Comprehensive Intervention for Changing Eating Habits Through Portion Control (PORTIONS_V_RCT)
Comprehensive Intervention for Changing Eating Habits Through Portion Control: PORTIONS-V Randomized Controlled Trial
This is a 12-month randomized controlled trial designed to evaluate the effectiveness of a comprehensive self-applied lifestlye intervention for weight loss, based on portion control. A total of 181 volunteers with overweight/obesity will be randomly allocated to an experimental intervention group or an active control group. The experimental intervention will include 4 components: (1) a portion control toolset (eating utensils); (2) a manual including instructions for the use of the tools, dietary and activity recommendations, and behavioural strategies; (3) a mobile app to motivate intervention engagement; and (4) a recipe book to help integrate the intervention in daily life. The control group will receive standard guidelines for healthy living, including diet and physical activity. Both groups will attend 4 clinical investigation days, 2 group sessions and will receive periodic telephone support. The primary outcome will be the change in waist circumference from baseline, assessed at 3, 9 and 12 months. Other measurements will include body composition, fasting biochemical parameters, eating behaviour, gut microbiota, functional magnetic resonance, portion size norms, intervention adherence and acceptance. The study will test the hypothesis that a comprehensive intervention focused on portion control can promote changes in eating habits and reduce waist circumference over 12 months compared with receving standard healthy living advice (active control group).
調査の概要
詳細な説明
Overweight and obesity are highly prevalent worldwide and represent major public health challenges. Nutritional interventions aimed at weight management frequently require sustained changes in eating behaviour, yet maintaining adherence to dietary recommendations over the long term remains challenging. Portion control represents a potentially useful strategy for promoting healthier eating habits, particularly through its potential effects on dietary energy density and meal composition. However, the mechanisms through which sustained changes in portion-related behaviours may influence body composition, metabolic health, eating behaviour and other physiological and cognitive processes remain insufficiently understood. Another challenge in nutritional intervention research is to assess dietary changes beyond their relationship with body weight alone. Changes in eating behaviour may be associated with metabolic markers, cognitive and behavioural processes, neural responses related to food intake, gut microbiota, and quality of life. A comprehensive assessment of these dimensions may therefore contribute to a better understanding of the factors associated with adherence to nutritional interventions and successful long-term weight management.
The primary objective of this randomized controlled trial is to confirm the effectiveness and long-term impact of a comprehensive weight management intervention focused on changing eating habits through portion control. The intervention is designed to facilitate the self-management of eating behaviour and promote sustained changes in the selection, composition and quantity of food consumed. The effect of the intervention will be assessed through changes in body composition at 3, 9 and 12 months, with change in waist circumference as the primary outcome. Secondary assessments will include metabolic, cognitive-behavioural and quality of life measures. The selection of these variables is informed by findings from the preceding PORTIONS-4 pilot study and by the scientific literature supporting the assessment of anthropometric and functional measures of adiposity in addition to weight and height-based indices such as body mass index (BMI), as well as comprehensive assessment of cognitive and behavioural factors, including habit formation, involved in eating and adherence.
The study will use a two-arm randomized controlled trial design, with participants allocated to either an experimental intervention group or a control group. A total of 181 participants will be enrolled, with 121 participants assigned to the experimental group and 60 to the control group. Participants allocated to the experimental group will receive a set of theoretical and practical strategies specifically developed or selected for this study to facilitate self-management of health and, in particular, the consumption of foods in recommended portions and quantities. The experimental intervention will consist of 4 complementary components: (1) an educational guide providing recommendations on nutrition, well-being and physical activity; (2) a toolset of optimized dietary tools consisting of a portion-serving spoon and a calibrated oil dispenser; (3) a recipe book specifically designed to provide healthy and sustainable recipes consistent with the intervention principles; and (4) a mobile application designed to support engagement with the intervention and facilitate the implementation of its recommendations in daily life. Participants allocated to the control group will receive an enhanced standard intervention based on theoretical nutrition education derived from recommendations provided by official health and nutrition organizations, together with recipes and physical activity guidelines. Both groups will participate in the intervention for 12 months, will receive six follow-up telephone calls throughout the intervention period and will receive the same degree of training and follow-up support, in order to minimize the potential influence of differences in contact level, education or support between groups.
The protocol includes clinical assessments at baseline and at 3, 9 and 12 months. Participants will also take part in two initial group sessions, two final group sessions and one central focus group (subsample) during the intervention period. At the scheduled clinical assessments, participants will undergo a comprehensive evaluation including biochemical measurements (glucose, insulin, lipid profile, ghrelin and glucagon-like peptide-1), body composition (assessed by bioelectrical impedance analysis) and physical function (handgrip strength assessment), psychological and quality-of-life questionnaires, eating rate and dietary composition. The study will also assess habit formation, food addiction, sensory and behavioural characteristics potentially related to eating behaviour, including taste detection thresholds. Changes in the gut microbiome will be evaluated to investigate potential biological adaptations associated with the intervention. In addition, functional magnetic resonance imaging will be used in a subsample to assess changes in neural activation and connectivity within networks involved in food-related processing and eating behaviour. These assessments will contribute to the investigation of potential interactions between eating behaviour, the gut microbiome and brain function during the weight management process.
The overall aim of these complementary assessments is to identify physiological, behavioural and cognitive mechanisms associated with adherence to and success of nutritional interventions for weight management. Understanding these mechanisms may contribute to the development of more personalized, effective and sustainable approaches to nutritional intervention. The primary hypothesis is that, compared with the control group, participants receiving the experimental intervention will show greater improvements in waist circumference and other measures of body composition over the 12-month intervention period. Improvements are also expected in BMI and fat mass. It is further hypothesized that participants in the experimental group will show greater improvements in dietary composition and in their ability to identify and apply appropriate portion sizes, reflected in healthier food choices and greater use of the portion-control strategies provided by the intervention. These effects are expected to be associated with greater utilization and adherence to the experimental intervention components. Compared with the control group, the experimental group is also expected to show more favourable changes in metabolic markers, cognitive and behavioural measures, and quality-of-life questionnaire scores over time. Finally, the study is expected to identify differences between groups in gut microbiota patterns and neural activation or connectivity associated with eating behaviour. Together, these findings may help clarify the physiological and cognitive mechanisms underlying adherence and response to comprehensive nutritional interventions for weight management.
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前:Eva Almiron Roig, PhD
- 電話番号:803316 34948425600
- メール:ealmiron@unav.es
研究連絡先のバックアップ
- 名前:Diego N Messina, PhD
- 電話番号:806346 34948425600
- メール:dmessinalom@unav.es
研究場所
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Navarre
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Pamplona、Navarre、スペイン、31008
- 募集
- University of Navarra, Centre for Nutrition Research
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コンタクト:
- Diego N Messina, PhD
- 電話番号:806346 34948425600
- メール:dmessinalom@unav.es
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コンタクト:
- Eva Almiron-Roig, PhD
- 電話番号:803316 34948425600
- メール:ealmiron@unav.es
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副調査官:
- Elkin O Luis, PhD
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副調査官:
- Verónica Aramendia, PhD
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副調査官:
- Fermín Milagro, PhD
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Body mass index equal or above 27.5 kg/m2 (26.0 kg/m2 for those of Asian descent), or waist circumference above 84 cm (female) or above 90 cm (male)
- Eating home-made meals at least 5 days a week
- Physically and mentally fit as assessed by the study researcher
- On-going pharmacological and hormonal treatment is accepted when this does not affect the study parameters (e.g., glucose response, appetite), and when the participant has been in a stable dose for at least 3 months
- Agreeing to undergo all the study procedures and consume the study foods
- Being able to attend in person on 4 clinical investigation days and 2 compulsory group sessions during working hours
- Being able to understand and agree to sign the informed consent form
Exclusion Criteria:
- Being a regular smoker (i.e., smoking more than 4 cigarettes a month)
- Being pregnant, breastfeeding or planning a pregnancy
- Exceed the weekly alcohol consumption limit for the corresponding sex (more than 14 units in women and more than 20 units in men)
- Having followed a meal plan for weight loss and/or muscle mass gain in the 3 months prior to the start of the study intervention
- Experiencing a weight change greater than 5% in the last 3 months
- History of relevant functional or structural anomalies of the digestive system, such as malformation, angiodysplasia, active peptic ulcer, chronic inflammatory or malabsorption disease, or history of intestinal or bariatric surgery
- Suffering from any type of cancer, currently undergoing treatment for cancer, or when a period of at least 5 years has not elapsed since its eradication
- On-going chronic metabolic disease or obesity-related disease, or any systemic intestinal, liver or kidney disease such as type 1 or type 2 diabetes, severe dyslipidemia, uncontrolled thyroid function disorder, cirrhosis, inflammatory bowel disease, untreated anemia, etc. (will not be excluded due to "fatty liver")
- Active mental health conditions, including dementia, that could interfere with the participant's ability to adequately follow the study protocol, or current use of psychiatric medications that may affect appetite (e.g., antidepressants). For stable-dose participants, cases will be evaluted on a one-to-one basis with the study medical team.
- Engaging in 10 or more hours of vigorous physical activity per week.
- Being allergic, or being intolerant to the study foods or their ingredients (regular or lactose-free yogurt and granola)
- History of anaphylactic reaction to any food
- Taking nutritional supplements as a prescription medication that may affect the results of the study
- Taking over-the-counter nutritional supplements (that is, without a medical prescription) that may affect the results of the study, unless the person is willing to stop it during the 12 months of the study duration and only when a minimum washout period of 14 days can be guaranteed prior to the basal measurements being taken
- A high incidence of attitudes and behaviors associated with eating disorders, expressed as a score greater than 20 on the 26-item Eating Attitudes Test scale (EAT - 26)
- Co-inhabiting with a study participant
- Previous participation in PORTIONS-3 (preclinical study) or PORTIONS-4 (pilot trial)
- For the body composition analysis, wearing a pacemaker or certain metallic implants.
ADDITIONAL EXCLUSION CRITERIA FOR SUB-STUDIES
Functional MRI sub-study - Additional Exclusion Criteria:
- Claustrophobia
- Presence of metallic implants, pacemakers, defibrillators, or other devices incompatible with functional magnetic resonance imaging (fMRI)
- Body weight greater than 180 kg
- Neck circumference greater than 62.8 cm
- Any contraindication to undergoing magnetic resonance imaging identified through the MRI safety screening questionnaire
- A score of 50% or lower for four or more of the food items included in the auditory stimuli in the food liking questionnaire, indicating insufficient familiarity with the stimuli
- Allocation to the trial's focus group discussions, unless the participant explicitly expresses a willingness to participate in both the fMRI assessment and the focus group discussions
Gut microbiota sub-study - Additional Exclusion Criteria
During the 15 days preceding stool sample collection:
- Use of antibiotics
- Use of fiber supplements
- Use of supplements that may affect the gut microbiota, such as probiotics or biotin
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
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実験的:Experimental intervention arm
Participants will receive a comprehensive 12-month intervention focused on changing eating habits through portion control. The intervention will include four components to promote lifestyle modification: (1) an educational guide with recommendations on nutrition, well-being and physical activity; (2) a portion-control toolset (calibrated oil dispenser and portion control serving spoon); (3) a healthy and sustainable recipe book; and (4) a mobile application to foster engagement with the intervention. Participants will also receive 6 follow-up telephone calls during the intervention period and will attend 4 clinical investigation days and 2 group sessions (with an additional 2 optional group sessions). A subsample of participants will undergo a focus group session (n=30) or functional magnetic resonance imaging (n=20). |
Self-applied, multicomponent intervention with a previously validated portion control toolset
他の名前:
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アクティブコンパレータ:Active control group
Participants will receive a 12-month enhanced standard intervention based on printed nutrition and physical activity recommendations/guidelines from official health and nutrition organizations (i.e., WHO). The intervention will include general dietary advice, recipes and physical activity guidelines. Participants will also receive 6 follow-up telephone calls during the intervention period and will attend 4 clinical investigation days and 2 group sessions (with an additional 2 optional group sessions). A subsample of participants will undergo a focus group session (n=15) or functional magnetic resonance imaging (n=10). |
Active comparator with same level of follow-up as experimental group
他の名前:
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
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Change in Waist Circumference From Baseline
時間枠:Week -1, Week 0, Week 12, Week 36, Week 48
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Change in waist circumference (cm) from baseline will be assessed over the 12-month intervention period. Waist circumference will be measured using standardized anthropometric procedures |
Week -1, Week 0, Week 12, Week 36, Week 48
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Change from baseline in dietary energy density (kcal/g)
時間枠:Week -1, Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Dietary energy (in kcal) and Dietary volume (in g) will be combined to obtain Dietary energy density (kcal/g). |
Week -1, Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Change from baseline in dietary nutrient composition (in g)
時間枠:Week -1, Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Dietary nutrient composition (in g) will be defined as the average % energy provided by macronutrients, obtained from the 24 h dietary record |
Week -1, Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Change from baseline in dietary nutrient composition (in % energy)
時間枠:Week -1, Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Dietary nutrient composition (in % energy) will be defined as the average % energy provided by macronutrients, obtained from the 24 h dietary record |
Week -1, Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Use of serving spoon (24 h frequency)
時間枠:Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Number of times the intervention spoon has been used in a period of 24 h (experimental arm only) |
Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Use of oil dispenser (24 h frequency)
時間枠:Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Number of times the oil dispenser has been used in a period of 24 h (experimental arm only) |
Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Use of intervention guide (24 h frequency)
時間枠:Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Number of times the intervention guide has been used in a period of 24 h |
Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Use of intervention app (24 h frequency)
時間枠:Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Number of times the intervention app has been used in a period of 24 h (experimental arm only) |
Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Use of cookbook (24 h frequency)
時間枠:Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Number of times the cookbook has been used in a period of 24 h |
Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Use of serving spoon (15 day frequency)
時間枠:Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Number of times the intervention spoon has been used in a period of 15 days (experimental arm only) |
Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Use of oil dispenser (15 day frequency)
時間枠:Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Number of times the oil dispenser has been used in a period of 15 days (experimental arm only) |
Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Use of intervention guide (15 day frequency)
時間枠:Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Number of times the intervention guide has been used in a period of 15 days |
Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Use of intervention app (15 day frequency)
時間枠:Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Number of times the intervention app has been used in a period of 15 days (experimental arm only) |
Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Use of cookbook (15 day frequency)
時間枠:Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Number of times the cookbook has been used in a period of 15 days |
Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Anthropometric profile: Body Height
時間枠:Week -1
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Height will be measured in m using a stadiometer |
Week -1
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Anthropometric profile: Body Weight
時間枠:Week -1, Week 0
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Weight will be measured in kg using Tanita scales |
Week -1, Week 0
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Anthropometric profile: Waist Circumference
時間枠:Week -1
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Waist circumference will be measured in cm using a measuring tape |
Week -1
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Anthropometric profile: Hip Circumference
時間枠:Week -1
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Hip circumference will be measured in cm using a measuring tape |
Week -1
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Anthropometric profile: Neck Circumference
時間枠:Week -1
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Neck circumference will be measured in cm using a measuring tape |
Week -1
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Anthropometric profile: Change from baseline in Body Weight
時間枠:Week 12, Week 36, Week 48
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Weight will be measured in kg |
Week 12, Week 36, Week 48
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Anthropometric profile: Change from baseline in Body Mass Index
時間枠:Week 12, Week 36, Week 48
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Body Mass Index will be calculated from weight and height as kg/m^2 |
Week 12, Week 36, Week 48
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Anthropometric profile: Change from baseline in Waist to Hip Ratio
時間枠:Week 12, Week 36, Week 48
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Waist to hip ratio is defined as the ratio of the waist circumference (cm) to the hip circumference (cm) |
Week 12, Week 36, Week 48
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Anthropometric profile: Change from baseline in body fat composition
時間枠:Week 0, Week 12, Week 36, Week 48
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Body fat composition will be quantified as fat mass (in kg, %) from a body composition analyser |
Week 0, Week 12, Week 36, Week 48
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Biochemical profile: Change from baseline in fasting blood glucose
時間枠:Week 0, Week 12, Week 36, Week 48
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Fasting blood glucose levels (mg/dL) |
Week 0, Week 12, Week 36, Week 48
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Biochemical profile: Change from baseline in fasting insulin
時間枠:Week 0, Week 12, Week 36, Week 48
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Fasting blood insulin levels (mIU/L) |
Week 0, Week 12, Week 36, Week 48
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Biochemical profile: Change from baseline in fasting blood triglycerides
時間枠:Week 0, Week 12, Week 36, Week 48
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Fasting blood triglycerides levels (mg/dL) |
Week 0, Week 12, Week 36, Week 48
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Biochemical profile: Change from baseline in fasting blood total cholesterol
時間枠:Week 0, Week 12, Week 36, Week 48
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Fasting blood total cholesterol levels (mg/dL) |
Week 0, Week 12, Week 36, Week 48
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Biochemical profile: Change from baseline in fasting blood HDL-cholesterol
時間枠:Week 0, Week 12, Week 36, Week 48
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Fasting blood HDL-cholesterol levels (mg/dL) |
Week 0, Week 12, Week 36, Week 48
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Biochemical profile: Change from baseline in fasting blood LDL-cholesterol
時間枠:Week 0, Week 12, Week 36, Week 48
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Fasting blood LDL- cholesterol levels (mg/dL) |
Week 0, Week 12, Week 36, Week 48
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Biochemical profile: Change from baseline in fasting blood ghrelin
時間枠:Week 0, Week 12, Week 36, Week 48
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Fasting blood ghrelin levels (pg/mL) |
Week 0, Week 12, Week 36, Week 48
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Biochemical profile: Change from baseline in fasting blood leptin
時間枠:Week 0, Week 12, Week 36, Week 48
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Fasting blood leptin levels (ng/mL) |
Week 0, Week 12, Week 36, Week 48
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Biochemical profile: Change from baseline in fasting blood GLP-1
時間枠:Week 0, Week 12, Week 36, Week 48
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Fasting blood GLP-1 levels (pmol/mL) |
Week 0, Week 12, Week 36, Week 48
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Meal eating behaviour: Change from baseline in Eating rate
時間枠:Week 0, Week 12, Week 36, Week 48
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Average amount of yogurt with granola consumed per unit of time (g/min), based on validated methodology (Yeomans, 2000) |
Week 0, Week 12, Week 36, Week 48
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Meal eating behaviour: Change from baseline in Bite Size
時間枠:Week 0, Week 12, Week 36, Week 48
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Average amount of yogurt with granola consumed at each bite (g), based on validated methodology (Yeomans, 2000) |
Week 0, Week 12, Week 36, Week 48
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Meal eating behaviour: Change from baseline in Meal Duration
時間枠:Week 0, Week 12, Week 36, Week 48
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Average time used to eat a yogurt with granola (min), based on validated methodology (Yeomans, 2000) |
Week 0, Week 12, Week 36, Week 48
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Meal eating behaviour: Change from baseline in Deceleration Rate
時間枠:Week 0, Week 12, Week 36, Week 48
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Average change in eating rate (g/sec-squared), based on validated methodology (Yeomans, 2000) |
Week 0, Week 12, Week 36, Week 48
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Learning task: Change from baseline in learned meal portion size
時間枠:Week 0, Week 12, Week 36, Week 48
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% error in chosen portion sizes for starch, protein and vegetables of a virtual meal vs recommended portion sizes (based on Brunstrom & Rogers, 2009) |
Week 0, Week 12, Week 36, Week 48
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Learning task: Change from baseline in learned meal nutrient content
時間枠:Week 0, Week 12, Week 36, Week 48
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% error in chosen nutrient content of a virtual meal vs recommended nutrient content (based on Brunstrom & Rogers, 2009) |
Week 0, Week 12, Week 36, Week 48
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Neural Activity Related to Food Reward Processing
時間枠:Week 0, Week 24, Week 48
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Neural activity associated with food reward and eating- related sensations, assessed using functional magnetic resonance imaging (fMRI) during exposure to food-related auditory stimuli, based on Carnell et al., 2017 (Subsample n=30 only) |
Week 0, Week 24, Week 48
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Gut Microbiota Diversity and Bacterial Abundance
時間枠:Week 0, Week 48
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Gut microbiota diversity and abundance of bacterial taxa associated with metabolic status, adiposity, mental health, and eating behavior |
Week 0, Week 48
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Food addiction
時間枠:Week -1, Week 24, Week 48
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Food addiction symptoms assessed using the Yale Food Addiction Scale (YFAS), validated by Granero et al., 2018 |
Week -1, Week 24, Week 48
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Habit Automaticity
時間枠:Week 1, Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Automaticity of eating-related habits assessed using the Self-Report Behavioural Automaticity Index (SRBAI), validated by Gardner et al., 2012 |
Week 1, Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Eating habits: Eating profile
時間枠:Week 0, Week 12, Week 36, Week 48
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Individual profile defined by the combined Restraint (0-21 points), Disihnibition (0-16 points) and Susceptibilty to hunger (0-14 points) sub-scales scores of the Three Factor Eating Questionnaire (TFEQ), validated by Stunkard & Messick, 1985. Restraint values above 11, disinhibition values above 8 and susceptibility to hunger values above 4 are considered worse outcomes (i.e. risk for development of obesity and other eating disorders) |
Week 0, Week 12, Week 36, Week 48
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Dietary energy (kcal)
時間枠:Week -1, Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Dietary energy (kcal) will be obtained from the 24 h dietary record |
Week -1, Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Dietary volume (in g)
時間枠:Week -1, Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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Dietary volume (g) will be obtained from the 24 h dietary record |
Week -1, Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
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その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Handgrip strength
時間枠:Week 0, Week 12, Week 36, Week 48
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Handgrip strength will be measured in kg using a dynamometer |
Week 0, Week 12, Week 36, Week 48
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Eating habits: Risk of eating disorders
時間枠:Week -1
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Score in the Eating Attitudes Test-26 (EAT-26), ranging from 0-78 points, validated by Garner et al., 1982. Scores above 20 suggest a higher risk for presence of potential eating disorders |
Week -1
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Physical activity level
時間枠:Week 0, Week 12, Week 36, Week 48
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Score in the short-form International Physical Activity Questionnaire (IPAQ), expressed as metabolic equivalent of task (MET)-minutes per week (Craig et al., 2003). Higher MET minutes indicates higher levels of physical activity. |
Week 0, Week 12, Week 36, Week 48
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Quality of Life (QoL)
時間枠:Week 0, Week 12, Week 36, Week 48
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Score in the World Health Organization Quality of Life-BREF (WHOQOL-BREF) questionnaire (The WHOQOL Group, 1998). Higher scores indicate a higher perception of quality of life. |
Week 0, Week 12, Week 36, Week 48
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Eating habits: Frequency of homemade meals
時間枠:Week -1
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Frequency of consuming homemade meals via self-reported questionnaire |
Week -1
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Eating habits: Frequency of take away meals
時間枠:Week -1
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Frequency of consuming take away meals via self-reported questionnaire |
Week -1
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Eating habits: Meal prep and serving
時間枠:Week -1
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Responsible person for cooking at home, via self-reported questionnaire |
Week -1
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Eating habits: Liking for the intervention food (yogurt with granola)
時間枠:Week -1, Week 0, Week 12, Week 36, Week 48
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Liking for the foods to be used in the intervention, via self-reported questionnaire (100 mm visual analogue scale) |
Week -1, Week 0, Week 12, Week 36, Week 48
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Eating habits: Familiarity with the intervention food (yogurt with granola)
時間枠:Week 0, Week 12, Week 36, Week 48
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Familiarity with the foods to be used in the intervention, via self-reported questionnaire (100 mm visual analogue scale) |
Week 0, Week 12, Week 36, Week 48
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Eating habits: Beverage consumption habits
時間枠:Week 0
|
Shortened version of the pre-piloted on-line Beverage Portion Size survey (Self-reported questionnaire assessing caloric beverage intake and awareness of beverage portion sizes) (Vargas-Alvarez et al., 2022) |
Week 0
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Eating habits: Problem Eating Behaviour Questionnaire (PEBQ)
時間枠:Week 0, Week 12, Week 36, Week 48
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Validated questionnaire (Carter & Jansen, 2012) used to identify eating patterns associated with the risk for obesity. It consists of 25 items answered on a 5-Pt intensity scale. The information collected can be used qualitatively, to identify problematic behaviors, or quantitatively by adding the direct scores. Scores greater than 50 suggest a moderate to high frequency of behaviors associated with obesity |
Week 0, Week 12, Week 36, Week 48
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Self-reported medical history
時間枠:Week -1
|
Self-reported questionnaire based on previous studies (Almiron-Roig et al., 2023) asking about special dietary needs, pregnancy, lactation, menopause, history of eating disorders, history of mental illness, incompatible medical conditions (e.g., cancer, diabetes, memory loss), regular medication including nutritional and other supplements |
Week -1
|
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Anthropometric profile: General body composition
時間枠:Week 0, Week 12, Week 36, Week 48
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Fat mass distribution (trunk, arms, legs), fat-free mass (kg, %), fat-free mass distribution, visceral fat score, basal metabolic rate (kcal/day) |
Week 0, Week 12, Week 36, Week 48
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Psychological profile: Personality
時間枠:Week -1
|
Score in the NEO-Five Factor Inventory (NEO-FFI) 60 item validated questionnaire (Costa & McCrae, 1989). The score for each central domain of normal personality defined by the Five-Factor Model of personality (neuroticism, extraversion, conscientiousness, agreeableness, and openness to experience) is calculated. A higher score on a scale assessing a certain personality domain indicates a stronger expression of traits associated with this particular domain |
Week -1
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Psychological profile: Perceived stress
時間枠:Week -1
|
Score in the Perceived Stress Scale-14 (PSS-14) validated questionnaire (Cohen et al., 1983). Scores ranging from 0 to 13 suggest low stress, scores ranging from 14 to 24 suggest moderate stress, and scores above 27 suggest high perceived stress |
Week -1
|
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Psychological profile: Emotional intelligence
時間枠:Week -1
|
Score in the Trait Meta-Mood Scale-24 (TMMS-24) validated questionnaire (Salovey et al., 1995). The score for three different dimensions of emotional intelligence are calculated. To obtain a score for each factor, items 1 to 8 are added for the emotional attention factor, items 9 to 16 for the emotional clarity factor, and items 17 to 24 for the emotional repair factor |
Week -1
|
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Psychological profile: Mood
時間枠:Week -1
|
Score in the Profile of Mood States (POMS) validated questionnaire (McNair et al., 1971). The score for six different dimensions of mood (tension, anger, fatigue, depression, confusion, and vigour) is calculated. A higher score on a scale assessing a certain mood dimension indicates a stronger expression of associated feelings. The resulting scores will range from -24 to 177, with lower scores indicative of people with more stable mood profiles |
Week -1
|
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Attitude towards intervention: Intervention expectations
時間枠:Week 0
|
Self-constructed scale evaluated with the sum of scores (1-10) for 5 items (based on Borkovec & Nau, 1972). The 5 items include rating the intervention's logic, satisfaction, recommendability, expected usefulness, and the respondent's readiness to follow it. A higher score reflects a more positive expectation towards the upcoming intervention |
Week 0
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Attitude towards intervention: Intervention opinion
時間枠:Week 12, Week 36
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Self-constructed scale evaluated with the sum of scores (1-10) for 5 items (based on Nau & Borkovec, 1972). The 5 items include rating the intervention's logic, satisfaction, recommendability, usefulness, and the respondent's readiness/intention to continue with it. A higher score reflects a more positive opinion towards the experienced intervention |
Week 12, Week 36
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Attitude towards intervention: Dietetic tool acceptance (serving spoon, oil dispenser)
時間枠:Week 12, Week 36, Week 48
|
Previously piloted questionnaire (Almiron-Roig et al., 2016) including 5-Pt Likert scores for portion tool attractiveness, fits within lifestyle, embarrassment, ease of use, perceived effectiveness and resistant to use. An average score of 1 or 2 indicates low acceptance, 3 neutral, and 4 or 5 high acceptance (experimental arm only) |
Week 12, Week 36, Week 48
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Attitude towards intervention: Dietetic tool intention to use (serving spoon, oil dispenser)
時間枠:Week 12, Week 36, Week 48
|
Single scale instrument measuring the level of intention to use each component from 0-100 on a 100 mm visual analogue scale (previously piloted questionnaire, Almiron-Roig et al., 2016) (experimental arm only) |
Week 12, Week 36, Week 48
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Attitude towards intervention: Perceived app usability
時間枠:Week 12, Week 36, Week 48
|
System Usability Scale (SUS) (based on Brooke, 1996). Includes ten 5-Pt Likert questions of which 5 items are scored positively (pleasant, easy to use, good functionality, quick to learn, safe), and 5 items are scored reversedly (complex, requires support, inconsistent, complicated to use, requires learning). A higher overall score indicates higher perceived usability (experimental arm only) |
Week 12, Week 36, Week 48
|
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Attitude towards intervention: App intention to use
時間枠:Week 12, Week 36, Week 48
|
Single scale instrument measuring the level of intention to use the intervention app from 0-100 on a 100 mm visual analogue scale (previously piloted questionnaire, Almiron-Roig et al., 2016) (experimental arm only) |
Week 12, Week 36, Week 48
|
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Attitude towards intervention: Intervention guide assessment
時間枠:Week 12
|
Self-constructed questionnaire including 20 items answered with a 5-Pt Likert scale. The first 10 items assess content of the guide (credibility, coherence, usefulness, applicability) and the second 10 items assess format (organisation, word choice and communication style). A score <60 indicates poor assessment (the tool cannot be used in clinical practice as it stands); a score between 60-79 indicates the tool needs revision before implementation; a score of 80 or above indicates the tool is well rated by potential users and may be useful in clinical practice |
Week 12
|
|
Attitude towards intervention: Intervention guide intention to use
時間枠:Week 12
|
Single scale instrument measuring the level of intention to use the intervention guide from 0-100 on a 100 mm visual analogue scale (previously piloted questionnaire, Almiron-Roig et al., 2016) |
Week 12
|
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Attitude towards intervention: Cookbook assessment
時間枠:Week 12
|
Self-constructed questionnaire including 6 items answered with a 5-Pt Likert scale. The items assess coherence, usefulness, applicability, contents, word choice and communication style. A score <18 indicates poor assessment (the tool cannot be used in clinical practice as it stands); a score between 18-24 indicates the tool needs revision before implementation; a score of 24 or above indicates the tool is well rated by potential users and may be useful in clinical practice |
Week 12
|
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Attitude towards intervention: Cookbook intention to use
時間枠:Week 12
|
Single scale instrument measuring the level of intention to use the Cookbook from 0-100 on a 100 mm visual analogue scale (previously piloted questionnaire, Almiron-Roig et al., 2016) |
Week 12
|
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Intervention component usage: serving spoon
時間枠:Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
|
Monthly questionnaire asking about types of meals in which the serving spoons were most frequently used in the last 2 weeks (experimental arm only) |
Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
|
|
Intervention component usage: oil dispenser
時間枠:Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
|
Monthly questionnaire asking about types of meals in which the oil dispenser was most frequently used in the last 2 weeks (experimental arm only) |
Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
|
|
Intervention component usage: intervention guide
時間枠:Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
|
Monthly questionnaire asking about guide sections most frequently checked in the last 2 weeks |
Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
|
|
Intervention component usage: Cookbook
時間枠:Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
|
Monthly questionnaire asking about cookbook sections most frequently checked in the last 2 weeks |
Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
|
|
Intervention component usage: intervention app
時間枠:Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
|
Monthly questionnaire asking about app functions most frequently used in the last 2 weeks (experimental arm only) |
Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48
|
|
Protocol compliance on clinical investigation days
時間枠:Week 0, Week 12, Week 36, Week 48
|
Self-constructed interview to verify participants' compliance with arrival time, physical activity and dietary requirements and any change in medication occurred prior to each clinical investigation day |
Week 0, Week 12, Week 36, Week 48
|
|
Taste detection
時間枠:Week 3, Weeks 40 to 44
|
Taste detection thresholds for bitter, sweet, sour, and salty tastes, assessed using paper taste strips impregnated with the corresponding taste stimuli |
Week 3, Weeks 40 to 44
|
|
Barriers to Intervention Adherence
時間枠:Weeks 21 to 24
|
Qualitative information on barriers to adherence encountered after 6 months of intervention, and participants' proposed solutions or strategies to overcome these barriers, collected through focus group discussions (subsample only n=45) |
Weeks 21 to 24
|
|
End of Study Survey
時間枠:Week 48
|
Self-constructed interview to assess participant's overall experience with the intervention at study end (items include previous tools/methods employed, satisfaction with intervention, consistency of use, barriers experienced and intention to continue using the components) |
Week 48
|
|
Adverse Events
時間枠:Week 6, Week 9, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 48, plus spontaneous contacts from participants
|
Adverse events are defined as any new unfavourable and unintended event that the participant has experienced during the course of the intervention or treatment. AE do not necessarily have a causal relationship with the intervention. Examples of AE may include:
Serious adverse events (SAE) are defined as any untoward medical occurrence that:
|
Week 6, Week 9, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 48, plus spontaneous contacts from participants
|
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Eating habits: Hunger levels
時間枠:Week 0, Week 12, Week 36, Week 48
|
Fasting scores for hunger measured on a 100 mm visual analogue scale, taken before consumption of yogurt with granola (validated questionnaire based on Hill & Blundell, 1982) |
Week 0, Week 12, Week 36, Week 48
|
|
Eating habits: Fullness levels
時間枠:Week 0, Week 12, Week 36, Week 48
|
Fasting scores for fullness measured on a 100 mm visual analogue scale, taken before consumption of yogurt with granola (validated questionnaire based on Hill & Blundell, 1982) |
Week 0, Week 12, Week 36, Week 48
|
|
Eating habits: Thirst levels
時間枠:Week 0, Week 12, Week 36, Week 48
|
Fasting scores for thirst measured on a 100 mm visual analogue scale, taken before consumption of yogurt with granola (validated questionnaire based on Hill & Blundell, 1982) |
Week 0, Week 12, Week 36, Week 48
|
|
Eating habits: Desire to eat levels
時間枠:Week 0, Week 12, Week 36, Week 48
|
Fasting scores for desire to eat measured on a 100 mm visual analogue scale, taken before consumption of yogurt with granola (validated questionnaire based on Hill & Blundell, 1982) |
Week 0, Week 12, Week 36, Week 48
|
|
Eating habits: Prospective intake levels
時間枠:Week 0, Week 12, Week 36, Week 48
|
Fasting scores for prospective intake measured on a 100 mm visual analogue scale, taken before consumption of yogurt with granola (validated questionnaire based on Hill & Blundell, 1982) |
Week 0, Week 12, Week 36, Week 48
|
|
Eating habits: Nausea levels
時間枠:Week 0, Week 12, Week 36, Week 48
|
Fasting scores for nausea measured on a 100 mm visual analogue scale, taken before consumption of yogurt with granola (validated questionnaire based on Hill & Blundell, 1982) |
Week 0, Week 12, Week 36, Week 48
|
|
Socio-demographic profile: Age
時間枠:Week -1
|
Age will be recorded in self-reported age in years at recruitment point |
Week -1
|
|
Socio-demographic profile: Sex
時間枠:Week -1
|
Sex will be recorded as self-reported sex assigned at birth (male, female) |
Week -1
|
|
Socio-demographic profile: Gender
時間枠:Week -1
|
Gender will be recorded as self-identified gender with one of these options: man, women, other (describe if you wish), prefer not to say. |
Week -1
|
|
Socio-demographic profile: Education
時間枠:Week -1
|
Education will be recorded as self-reported maximum education level achieved with one these options: without education; prmary education; secondary education; seconary vocational education; high vocational education; university degree; other (specify). |
Week -1
|
|
Socio-demographic profile: marital status
時間枠:Week -1
|
Marital status will be recorded as self-reported status with one of these options: married, civil union, separated, divorced, widowed, single (never married), other (specify). |
Week -1
|
|
Socio-demographic profile: Country of birth
時間枠:Week -1
|
Self-reported country of birth will be recorded using an open-ended question "country of birth" |
Week -1
|
|
Socio-demographic profile: Employment
時間枠:Week -1
|
Employment will be recorded as self-reported professional situation with one of these open-ended questions: Current job (if you have); Last job (in case of retirement, permanent leave, unemployment, etc.); Without a current or past job |
Week -1
|
|
Socio-demographic profile: Smoking status
時間枠:Week -1
|
Smoking status will be recorded as self-reported habits with one of these options: never smoked; ex-smoker (for more than 3 months); current smoker; occasional smoker (fewer than 4 cigarettes per month). |
Week -1
|
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Socio-demographic profile: alcohol intake
時間枠:Week -1
|
Alcohol intake will be recorded as self-reported weekly alcohol unit consumption (1 unit = can, glass or shot). |
Week -1
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協力者と研究者
捜査官
- 主任研究者:Eva Almiron-Roig, PhD、University of Navarra
出版物と役立つリンク
一般刊行物
- Cohen S, Kamarck T, Mermelstein R. A global measure of perceived stress. J Health Soc Behav. 1983 Dec;24(4):385-96. No abstract available.
- Stunkard AJ, Messick S. The three-factor eating questionnaire to measure dietary restraint, disinhibition and hunger. J Psychosom Res. 1985;29(1):71-83. doi: 10.1016/0022-3999(85)90010-8.
- Craig CL, Marshall AL, Sjostrom M, Bauman AE, Booth ML, Ainsworth BE, Pratt M, Ekelund U, Yngve A, Sallis JF, Oja P. International physical activity questionnaire: 12-country reliability and validity. Med Sci Sports Exerc. 2003 Aug;35(8):1381-95. doi: 10.1249/01.MSS.0000078924.61453.FB.
- Development of the World Health Organization WHOQOL-BREF quality of life assessment. The WHOQOL Group. Psychol Med. 1998 May;28(3):551-8. doi: 10.1017/s0033291798006667.
- Garner DM, Olmsted MP, Bohr Y, Garfinkel PE. The eating attitudes test: psychometric features and clinical correlates. Psychol Med. 1982 Nov;12(4):871-8. doi: 10.1017/s0033291700049163.
- Almiron-Roig E, Dominguez A, Vaughan D, Solis-Trapala I, Jebb SA. Acceptability and potential effectiveness of commercial portion control tools amongst people with obesity. Br J Nutr. 2016 Dec;116(11):1974-1983. doi: 10.1017/S0007114516004104. Epub 2016 Dec 15.
- Gardner B, Abraham C, Lally P, de Bruijn GJ. Towards parsimony in habit measurement: testing the convergent and predictive validity of an automaticity subscale of the Self-Report Habit Index. Int J Behav Nutr Phys Act. 2012 Aug 30;9:102. doi: 10.1186/1479-5868-9-102.
- Vargas-Alvarez MA, Quiroz V, Martinez JA, Almiron-Roig E. Development and piloting of an on-line questionnaire to assess portion size knowledge and consumption habits of non-alcoholic beverages. Appetite. 2022 Feb;169:105555. doi:10.1016/j.appet.2021.105555
- McNair DM, Lorr M, Droppleman LF. Manual for the Profile of Mood States. San Diego, CA: Educational and Industrial Testing Service; 1971
- Costa PT Jr, McCrae RR. NEO PI/FFI manual supplement for use with the NEO Personality Inventory and the NEO Five-Factor Inventory. Odessa, FL: Psychological Assessment Resources; 1989.
- Brooke J. SUS: a quick and dirty usability scale. In: Jordan PW, Thomas B, McClelland IL, Weerdmeester B, editors. Usability Evaluation in Industry. London: Taylor & Francis; 1996. p. 189-194
- Borkovec TD, Nau SD. Credibility of analogue therapy rationales. J Behav Ther Exp Psychiatry. 1972 Dec;3(4):257-260. doi:10.1016/0005-7916(72)90045-6.
- Yeomans MR. Rating changes over the course of meals: what do they tell us about motivation to eat? Neurosci Biobehav Rev. 2000 Mar;24(2):249-59. doi: 10.1016/s0149-7634(99)00078-0.
- Hill AJ, Blundell JE. Nutrients and behaviour: research strategies for the investigation of taste characteristics, food preferences, hunger sensations and eating patterns in man. J Psychiatr Res. 1982-1983;17(2):203-12. doi: 10.1016/0022-3956(82)90023-1.
- Granero R, Jimenez-Murcia S, Gearhardt AN, Aguera Z, Aymami N, Gomez-Pena M, Lozano-Madrid M, Mallorqui-Bague N, Mestre-Bach G, Neto-Antao MI, Riesco N, Sanchez I, Steward T, Soriano-Mas C, Vintro-Alcaraz C, Menchon JM, Casanueva FF, Dieguez C, Fernandez-Aranda F. Validation of the Spanish Version of the Yale Food Addiction Scale 2.0 (YFAS 2.0) and Clinical Correlates in a Sample of Eating Disorder, Gambling Disorder, and Healthy Control Participants. Front Psychiatry. 2018 May 25;9:208. doi: 10.3389/fpsyt.2018.00208. eCollection 2018.
- Carter FA, Jansen A. Improving psychological treatment for obesity. Which eating behaviours should we target? Appetite. 2012 Jun;58(3):1063-9. doi: 10.1016/j.appet.2012.01.016. Epub 2012 Jan 25.
- Carnell S, Benson L, Chang KV, Wang Z, Huo Y, Geliebter A, Peterson BS. Neural correlates of familial obesity risk and overweight in adolescence. Neuroimage. 2017 Oct 1;159:236-247. doi: 10.1016/j.neuroimage.2017.07.052. Epub 2017 Jul 25.
- Brunstrom JM, Rogers PJ. How many calories are on our plate? Expected fullness, not liking, determines meal-size selection. Obesity (Silver Spring). 2009 Oct;17(10):1884-90. doi: 10.1038/oby.2009.201. Epub 2009 Jun 18.
- Almiron-Roig E, Navas-Carretero S, Castelnuovo G, Kjolbaek L, Romo-Hualde A, Normand M, Maloney N, Hardman CA, Hodgkins CE, Moshoyiannis H, Finlayson G, Scott C, Raats MM, Harrold JA, Raben A, Halford JCG, Martinez JA. Impact of acute consumption of beverages containing plant-based or alternative sweetener blends on postprandial appetite, food intake, metabolism, and gastro-intestinal symptoms: Results of the SWEET beverages trial. Appetite. 2023 May 1;184:106515. doi: 10.1016/j.appet.2023.106515. Epub 2023 Feb 26.
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研究開始 (推定)
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研究の完了 (推定)
試験登録日
最初に提出
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最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
- PC24-PORTIONS-V-007-002
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