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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).

Studieöversikt

Detaljerad beskrivning

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.

Studietyp

Interventionell

Inskrivning (Beräknad)

181

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

  • Namn: Eva Almiron Roig, PhD
  • Telefonnummer: 803316 34948425600
  • E-post: ealmiron@unav.es

Studera Kontakt Backup

Studieorter

    • Navarre
      • Pamplona, Navarre, Spanien, 31008
        • Rekrytering
        • University of Navarra, Centre for Nutrition Research
        • Kontakt:
        • Kontakt:
          • Eva Almiron-Roig, PhD
          • Telefonnummer: 803316 34948425600
          • E-post: ealmiron@unav.es
        • Underutredare:
          • Elkin O Luis, PhD
        • Underutredare:
          • Verónica Aramendia, PhD
        • Underutredare:
          • Fermín Milagro, PhD

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år till 70 år (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Ja

Kön som är behöriga för studier

Allt

Beskrivning

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

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: 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

Andra namn:
  • Beteendeförändring
  • Livsstilsförändring
Aktiv komparator: 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

Andra namn:
  • Beteendeförändring

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Change in Waist Circumference From Baseline
Tidsram: Week -1, Week 0, Week 12, Week 36, Week 48

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

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Change from baseline in dietary energy density (kcal/g)
Tidsram: 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

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
Change from baseline in dietary nutrient composition (in g)
Tidsram: 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

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
Change from baseline in dietary nutrient composition (in % energy)
Tidsram: 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

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
Use of serving spoon (24 h frequency)
Tidsram: Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48

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
Use of oil dispenser (24 h frequency)
Tidsram: Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48

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
Use of intervention guide (24 h frequency)
Tidsram: Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48

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
Use of intervention app (24 h frequency)
Tidsram: Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48

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
Use of cookbook (24 h frequency)
Tidsram: Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48

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
Use of serving spoon (15 day frequency)
Tidsram: Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48

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
Use of oil dispenser (15 day frequency)
Tidsram: Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48

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
Use of intervention guide (15 day frequency)
Tidsram: Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48

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
Use of intervention app (15 day frequency)
Tidsram: Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48

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
Use of cookbook (15 day frequency)
Tidsram: Week 4, Week 8, Week 12, Week 16, Week 20, Week 24, Week 28, Week 32, Week 36, Week 40, Week 44, Week 48

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
Anthropometric profile: Body Height
Tidsram: Week -1

Height will be measured in m using a stadiometer

Week -1
Anthropometric profile: Body Weight
Tidsram: Week -1, Week 0

Weight will be measured in kg using Tanita scales

Week -1, Week 0
Anthropometric profile: Waist Circumference
Tidsram: Week -1

Waist circumference will be measured in cm using a measuring tape

Week -1
Anthropometric profile: Hip Circumference
Tidsram: Week -1

Hip circumference will be measured in cm using a measuring tape

Week -1
Anthropometric profile: Neck Circumference
Tidsram: Week -1

Neck circumference will be measured in cm using a measuring tape

Week -1
Anthropometric profile: Change from baseline in Body Weight
Tidsram: Week 12, Week 36, Week 48

Weight will be measured in kg

Week 12, Week 36, Week 48
Anthropometric profile: Change from baseline in Body Mass Index
Tidsram: Week 12, Week 36, Week 48

Body Mass Index will be calculated from weight and height as kg/m^2

Week 12, Week 36, Week 48
Anthropometric profile: Change from baseline in Waist to Hip Ratio
Tidsram: Week 12, Week 36, Week 48

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
Anthropometric profile: Change from baseline in body fat composition
Tidsram: Week 0, Week 12, Week 36, Week 48

Body fat composition will be quantified as fat mass (in kg, %) from a body composition analyser

Week 0, Week 12, Week 36, Week 48
Biochemical profile: Change from baseline in fasting blood glucose
Tidsram: Week 0, Week 12, Week 36, Week 48

Fasting blood glucose levels (mg/dL)

Week 0, Week 12, Week 36, Week 48
Biochemical profile: Change from baseline in fasting insulin
Tidsram: Week 0, Week 12, Week 36, Week 48

Fasting blood insulin levels (mIU/L)

Week 0, Week 12, Week 36, Week 48
Biochemical profile: Change from baseline in fasting blood triglycerides
Tidsram: Week 0, Week 12, Week 36, Week 48

Fasting blood triglycerides levels (mg/dL)

Week 0, Week 12, Week 36, Week 48
Biochemical profile: Change from baseline in fasting blood total cholesterol
Tidsram: Week 0, Week 12, Week 36, Week 48

Fasting blood total cholesterol levels (mg/dL)

Week 0, Week 12, Week 36, Week 48
Biochemical profile: Change from baseline in fasting blood HDL-cholesterol
Tidsram: Week 0, Week 12, Week 36, Week 48

Fasting blood HDL-cholesterol levels (mg/dL)

Week 0, Week 12, Week 36, Week 48
Biochemical profile: Change from baseline in fasting blood LDL-cholesterol
Tidsram: Week 0, Week 12, Week 36, Week 48

Fasting blood LDL- cholesterol levels (mg/dL)

Week 0, Week 12, Week 36, Week 48
Biochemical profile: Change from baseline in fasting blood ghrelin
Tidsram: Week 0, Week 12, Week 36, Week 48

Fasting blood ghrelin levels (pg/mL)

Week 0, Week 12, Week 36, Week 48
Biochemical profile: Change from baseline in fasting blood leptin
Tidsram: Week 0, Week 12, Week 36, Week 48

Fasting blood leptin levels (ng/mL)

Week 0, Week 12, Week 36, Week 48
Biochemical profile: Change from baseline in fasting blood GLP-1
Tidsram: Week 0, Week 12, Week 36, Week 48

Fasting blood GLP-1 levels (pmol/mL)

Week 0, Week 12, Week 36, Week 48
Meal eating behaviour: Change from baseline in Eating rate
Tidsram: Week 0, Week 12, Week 36, Week 48

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
Meal eating behaviour: Change from baseline in Bite Size
Tidsram: Week 0, Week 12, Week 36, Week 48

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
Meal eating behaviour: Change from baseline in Meal Duration
Tidsram: Week 0, Week 12, Week 36, Week 48

Average time used to eat a yogurt with granola (min), based on validated methodology (Yeomans, 2000)

Week 0, Week 12, Week 36, Week 48
Meal eating behaviour: Change from baseline in Deceleration Rate
Tidsram: Week 0, Week 12, Week 36, Week 48

Average change in eating rate (g/sec-squared), based on validated methodology (Yeomans, 2000)

Week 0, Week 12, Week 36, Week 48
Learning task: Change from baseline in learned meal portion size
Tidsram: Week 0, Week 12, Week 36, Week 48

% 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
Learning task: Change from baseline in learned meal nutrient content
Tidsram: Week 0, Week 12, Week 36, Week 48

% 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
Neural Activity Related to Food Reward Processing
Tidsram: Week 0, Week 24, Week 48

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
Gut Microbiota Diversity and Bacterial Abundance
Tidsram: Week 0, Week 48

Gut microbiota diversity and abundance of bacterial taxa associated with metabolic status, adiposity, mental health, and eating behavior

Week 0, Week 48
Food addiction
Tidsram: Week -1, Week 24, Week 48

Food addiction symptoms assessed using the Yale Food Addiction Scale (YFAS), validated by Granero et al., 2018

Week -1, Week 24, Week 48
Habit Automaticity
Tidsram: 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

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
Eating habits: Eating profile
Tidsram: Week 0, Week 12, Week 36, Week 48

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
Dietary energy (kcal)
Tidsram: 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

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
Dietary volume (in g)
Tidsram: 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

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

Andra resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Handgrip strength
Tidsram: Week 0, Week 12, Week 36, Week 48

Handgrip strength will be measured in kg using a dynamometer

Week 0, Week 12, Week 36, Week 48
Eating habits: Risk of eating disorders
Tidsram: Week -1

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
Physical activity level
Tidsram: Week 0, Week 12, Week 36, Week 48

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
Quality of Life (QoL)
Tidsram: Week 0, Week 12, Week 36, Week 48

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
Eating habits: Frequency of homemade meals
Tidsram: Week -1

Frequency of consuming homemade meals via self-reported questionnaire

Week -1
Eating habits: Frequency of take away meals
Tidsram: Week -1

Frequency of consuming take away meals via self-reported questionnaire

Week -1
Eating habits: Meal prep and serving
Tidsram: Week -1

Responsible person for cooking at home, via self-reported questionnaire

Week -1
Eating habits: Liking for the intervention food (yogurt with granola)
Tidsram: Week -1, Week 0, Week 12, Week 36, Week 48

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
Eating habits: Familiarity with the intervention food (yogurt with granola)
Tidsram: Week 0, Week 12, Week 36, Week 48

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
Eating habits: Beverage consumption habits
Tidsram: 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
Eating habits: Problem Eating Behaviour Questionnaire (PEBQ)
Tidsram: Week 0, Week 12, Week 36, Week 48

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
Self-reported medical history
Tidsram: 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
Anthropometric profile: General body composition
Tidsram: Week 0, Week 12, Week 36, Week 48

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
Psychological profile: Personality
Tidsram: 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
Psychological profile: Perceived stress
Tidsram: 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
Psychological profile: Emotional intelligence
Tidsram: 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
Psychological profile: Mood
Tidsram: 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
Attitude towards intervention: Intervention expectations
Tidsram: 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
Attitude towards intervention: Intervention opinion
Tidsram: Week 12, Week 36

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
Attitude towards intervention: Dietetic tool acceptance (serving spoon, oil dispenser)
Tidsram: 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
Attitude towards intervention: Dietetic tool intention to use (serving spoon, oil dispenser)
Tidsram: 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
Attitude towards intervention: Perceived app usability
Tidsram: 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
Attitude towards intervention: App intention to use
Tidsram: 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
Attitude towards intervention: Intervention guide assessment
Tidsram: 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
Tidsram: 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
Attitude towards intervention: Cookbook assessment
Tidsram: 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
Attitude towards intervention: Cookbook intention to use
Tidsram: 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
Intervention component usage: serving spoon
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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:

  • Abnormal laboratory findings
  • Symptoms (e.g. gastro-intestinal discomfort, headache)
  • Disease
  • Worsening of existing symptoms

Serious adverse events (SAE) are defined as any untoward medical occurrence that:

  • Results in death
  • Is life-threatening at the time of the event
  • Requires in-patient hospitalization as in extension of an already planned hospitalization or requiring a new (unplanned) hospitalization
  • Results in persistent or significant disability or incapacity
  • Is another important medical event
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
Eating habits: Hunger levels
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: Week -1

Age will be recorded in self-reported age in years at recruitment point

Week -1
Socio-demographic profile: Sex
Tidsram: Week -1

Sex will be recorded as self-reported sex assigned at birth (male, female)

Week -1
Socio-demographic profile: Gender
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: Week -1

Self-reported country of birth will be recorded using an open-ended question "country of birth"

Week -1
Socio-demographic profile: Employment
Tidsram: 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
Tidsram: 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
Socio-demographic profile: alcohol intake
Tidsram: Week -1

Alcohol intake will be recorded as self-reported weekly alcohol unit consumption (1 unit = can, glass or shot).

Week -1

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Samarbetspartners

Utredare

  • Huvudutredare: Eva Almiron-Roig, PhD, University of Navarra

Publikationer och användbara länkar

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Allmänna publikationer

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Beräknad)

15 oktober 2026

Primärt slutförande (Beräknad)

29 januari 2028

Avslutad studie (Beräknad)

29 februari 2028

Studieregistreringsdatum

Först inskickad

3 november 2026

Först inskickad som uppfyllde QC-kriterierna

9 november 2026

Första postat (Faktisk)

12 november 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

12 november 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

9 november 2026

Senast verifierad

1 september 2026

Mer information

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