- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06360432
Effects of the EatWelLog App on Diet Management for Older Adults With Sarcopenic Obesity
Effects of the EatWelLog App on Enhancing Daily Diet Management for Community-dwelling Older Adults With Sarcopenic Obesity: A Pilot Randomized Controlled Trial
Sarcopenic obesity, characterised by concurrent reduced muscle mass and excess body fat, affects 11% of older adults worldwide, rising to 23% in those over 75. Considering the negative synergistic impact on health, promoting muscle mass gains while reducing fat mass remains a significant challenge, necessitating urgent and effective intervention strategies for managing SO. Exercise and nutrition are the primary interventions recommended for SO.
This project aims to evaluate the effects of the EatWellLog App developed by the investigators' team for local older adults, in improving:
- their sarcopenic obesity status, measured by all four diagnostic criteria, including grip strength, muscle mass, physical performance and body fat mass (primary outcome), and,
- nutritional self-efficacy, nutritional status, dietary quality, health-related quality of life, and adherence to diet and exercise regimens (secondary outcomes), by enhancing the self-management abilities and longer-term adherence to daily diet management among participants in the M-health group using the App, compared to the control group.
The EatWellLog App, designed for older adults with SO, incorporating Klasnja and Pratt's five-strategy framework for mobile health (mHealth) applications development to facilitate health behavioural change. This App supports users with SO in managing daily diets that promote gradual weight loss and muscle mass preservation, adhering to the dietary regimen for this population.
Forty older adults with SO will be recruited from local community health centres and then randomized to either m-health or control groups. Both groups will receive an 8-week supervised programme separately. The programme consists of personalised dietary modification programme and group-based exercise training which have been tested and used in the investigators' pilot and General Research Fund (GRF) project. Additionally, only the m-health group will be instructed to use the App for daily diet self-management.
Participants will be assessed on a variety of outcomes immediately after the 8-week supervised programme (T1), which will be compared to the baseline (T0). To explore the possible long-term effects of the intervention, other measurements will be conducted at 3-(T2) and 6-(T3) months after the supervised programme, which will be compared with those conducted at T0.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Sarcopenic obesity (SO), characterized by concurrent reduced muscle mass and excess body fat, affects 11% older adults worldwide, rising to 23% among those over 751. Older adults with reduced muscle mass are 1.95-2.62 times prone to obesity than those with normal muscle mass. This is due to shared etiological factors between sarcopenia and obesity such as sedentary habits and aging-related biological shifts, including decreased anabolic hormones, increased insulin resistance, and escalated oxidative stress. The combination of sarcopenia and obesity has a compounding negative impact on health, raising the likelihood of knee and hip osteoarthritis, which leads to reduced physical capabilities, as well as increasing the risk of cardio-metabolic diseases, institutionalized, and death, exceeding the risks of sarcopenia or obesity alone.
Addressing SO effectively to promote muscle mass gains while reducing fat mass remains a significant challenge, necessitating urgent and effective intervention strategies. Currently, exercise and nutrition interventions, are the most commonly recommended interventions.
Exercise and Nutrition Interventions for SO A recent systematic review of 11 trials with 440 SO participants showed that resistance training twice weekly for 20 minutes over a minimum of 8 weeks effectively enhances body composition, muscle strength, and gait speed. Furthermore, evidence suggested that combining aerobic and resistance training with increased protein intake is more effective in reducing body fat than resistance training alone but had no effects on muscle mass and strength. Another systematic review of eight trials with 605 SO participants found that resistance training alone could increase muscle strength. To also improve physical functions (i.e., gait speed and grip strength), exercise combining aerobic and resistance training with dietary supplements seems to have more promising results. The findings in a recent umbrella review of meta-analyses concluded that exercise interventions (either resistance training or combined resistance and aerobic exercise) are beneficial for body composition and physical performance in older adults with SO. However, the added value of exercise with nutrition interventions (either protein supplement and dietary modifications) produces inconsistent results.
Adequate protein intake is vital for muscle building, and calorie restriction is effective at reducing fat mass. Thus, nutrition is a critical factor in the onset and progression of SO, although the evidence for nutrition interventions in reserving SO demonstrated inconsistent effects, especially regarding muscle mass and strength. When implementing a weight loss diet for individuals with SO, it is important to balance fat reduction with muscle mass preservation by ensure adequate protein intake to prevent exacerbating muscle loss. Evidence suggests that the source of protein is crucial for muscle retention, specifically for animal-based proteins, which are high in leucine, may be more effective in preserving muscle mass during weight loss and in maintaining physical function. While nutritional supplements are commonly used to increase protein intake, their effects on SO remain inconsistent and may cause side effects such as digestive issues, interact with certain medications, dehydration, liver and renal damage, bloating, and calcium loss. The investigators advocates for an unhealthy diet incorporating a full spectrum of nutrients from whole foods, in line with the Dietary Guidelines for Americans, 2020-2025, as the preferred approach over supplements for those with sarcopenic obesity. Modifying daily dietary habits of individuals with SO may provide more sustainable benefits than merely adding supplements to their diet.
A recent systematic review examining nutrition interventions in managing sarcopenic obesity analysed nine studies but only two assessed the impact of dietary modifications on protein intake among older adults with SO. The first randomized controlled trial (RCT) assessed the impact of a low-calorie diet with normal (0.8 g/kg body weight/day) versus high protein intake (1.2 g/kg body weight/day) over three months in 104 older women with SO. The study found muscle mass decreased in the normal protein group concurrent with fat loss, while the high protein group saw muscle mass preservation. The second pilot RCT involving 18 women compared a low-calorie diet with placebo to one with high protein (1.2-1.4 g/kg body weight/day) over four months. Significant muscle strength gains were noted in the high protein group, though changes in muscle mass were not significantly different between the two groups. While the findings in these two trials provided preliminary evidence that hypocaloric diet and high protein intake may be necessary for managing SO, particularly for preserving mass muscle and strength. These studies, however, had limitations such as broad inclusion criteria for sarcopenic obesity, lacking a standardized diagnostic protocol, insufficient data on dietary adherence, and opaque details regarding randomization and intervention specifics. More rigorous research is needed to investigate the impact of diet modification on sarcopenic obesity.
Conventional dietary modification intervention that relies on face-to-face consultation and monitoring, faced lots of challenges which included participants' poor compliance to the recommended dietary regimen, high attrition, time constraints and manpower. Those were major threats to the viability of the study leading to inconsistent treatment effects. In addition, the therapeutic effect may gradually reduces after the completion of the dietary training program. Additionally, the therapeutic effect may gradually reduce after the completion of the dietary program.
Rationale for developing a m-health based intervention for SO Systematic reviews found that m-health dietary intervention, with appropriate behaviour change techniques, can achieve dietary behaviour change across a range of chronic illnesses, such as obesity, metabolic syndrome, cardiovascular disease with relatively low attrition rates. To the best of the knowledge, there are no studies evaluating the effects of m-health dietary interventions on SO. The success of m-health interventions in other chronic conditions could potentially be adapted to improve health behaviors in patients with SO.
Aims and Hypotheses to be Tested.
The study aims to evaluate the effects of the EatWellLog App (hereafter referred to as "the App"), designed by the investigators' team to address the needs of local older adults, in improving:
- their sarcopenic obesity status, measured by all four diagnostic criteria, including grip strength, muscle mass, physical performance and body fat mass (primary outcome), and,
- nutritional self-efficacy, nutritional status, dietary quality, health-related quality of life, and adherence to diet and exercise regimens (secondary outcomes), by enhancing the self-management abilities and longer-term adherence to daily diet management among participants in the M-health group using the App, compared to the control group.
It is hypothesised that the App users will demonstrate significant and sustained improvements in SO status and secondary outcomes immediately after the supervised nutrition and exercise programme and at 3-and 6-month follow ups, compared to the control group who receive the same supervised programme without the App.
The investigators will also explore users' experience with the App by focus groups with all participants in the M-health group, 6-8 per group, to understand their experience of using the App. Additionally, the investigators will analyse the App usage data including session duration, frequency, feature utilisation, and retention rates, at the 3-month and 6-month follow-ups.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Justina Liu, PhD
- Phone Number: 27666427
- Email: justina.liu@polyu.edu.hk
Study Contact Backup
- Name: Amy Cheung
- Phone Number: 27664145
- Email: amy-ka-po.cheung@polyu.edu.hk
Study Locations
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Hong Kong, Hong Kong
- The Hong Kong Polytechnic University
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Contact:
- Amy Cheung, MA
- Phone Number: +852 27664145
- Email: amy-ka-po.cheung@polyu.edu.hk
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Aged 65 or above, and living in the community;
Having SO according to the Asian Working Group for Sarcopenia (AWGS) and the World Health Organization (WHO)'s obesity criteria for Asians:
- Early-stage sarcopenia indicated by fulfilment of one of the following criteria; handgrip strength <28 kg (men) and <18 kg (women); appendicular skeletal muscle mass (ASM)/ height2 <7 kg/m2 (men) and <5.7 kg/m2 (women), or SPPB score of <9; Short Physical Performance Battery (SPPB) score of <9,
- Obesity indicated by BMI ≥25 kg/m2, waist circumference ≥90 cm (men) and ≥80 cm (women), or body fat >30%;
- Own a smartphone with internet access; and
- Proficiency in communicating, reading, and writing in Chinese, and without major hearing and vision impairments to ensure that comprehension of our instructions.
Exclusion Criteria:
- Individuals with diseases impacting digestion or food consumption, including severe cardiac/ pulmonary/ renal diseases, diabetes, cancer, or autoimmune disorders;
- Those on medications affecting eating habits, digestion, or metabolism, such as weight loss drugs;
- Persons with alcohol use disorder as defined by the Diagnostic and Statistical Manual of Mental Disorders (DSM-5), potentially hindering dietary behaviour changes;
- Those with medical implants like pacemakers that could be disrupted by the bioelectric impedance analysis (BIA's) low-level electrical currents.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: M-health group
Participants in the M-health will receive an 8-week program consisting of personalized dietary modification program and group-based exercise training.
Additionally, the m-health group will be instructed to use the EatWellLog app for daily diet self-management.
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Participants will receive an 8-week program consisting of personalized dietary modification program.
The dietary modification program is composed of a total of 8 personalized, one-hour face-to-face sessions.
Participants will be encouraged to take on a moderate hypocaloric plan that cuts daily energy expenditure to encourage steady weight loss while preserving muscle mass.
A protein intake of 1.5 g/kg of body weight per day is recommended.
To optimize protein uptake, it's suggested that protein be distributed evenly across meals, aiming for 25-30 g per meal, inclusive of 2.5-2.8
g of leucine.
Participants will also receive a guidebook, crafted through the Delphi method, to facilitate the adoption of these dietary modifications in their daily routines.
Participants will receive an 8-week program consisting of exercise training.
It entails weekly group sessions, with each lasting an hour for 8 weeks.
These sessions, designed for groups of approximately 10, will blend resistance and aerobic workouts to enhance muscle mass and strength while reducing fat in individuals with SO.
Each session includes a 10-minute warm-up and cool-down, 20 minutes of resistance training using elastic bands, followed by a 20-minute brisk walking segment.
Participants will also receive a YouTube link and a pamphlet describing the exercises, encouraging them to maintain at least 30 minutes of exercise five times a week during and beyond the supervised programme.
Only participants in the M-health group will be instructed to use the EatWellLog app for daily diet self-management.
This App supports participants with SO by providing a structured approach to managing a diet that encourages steady weight loss while maintaining muscle mass, in line with current nutritional recommendations for this demographic.
The EatWellLog App has the following features: i) tracking participants' dietary habits by logging meals and snacks from a food list, ii) personalized online coaching and reminders by a multidisciplinary healthcare team, iii) participation of family caregivers through an interactive messaging function, iv) accessing health information via multiple channels, including animations, an at-a-glance display, and a reminder, and v) utilization of game elements, such as educational animations and video games to disseminate health and nutritional information related to SO.
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Sham Comparator: Control group
Participants in the Control group will receive an identical, 8-week program consisting of personalized dietary modification program and group-based exercise training without using the EatWellLog App.
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Participants will receive an 8-week program consisting of personalized dietary modification program.
The dietary modification program is composed of a total of 8 personalized, one-hour face-to-face sessions.
Participants will be encouraged to take on a moderate hypocaloric plan that cuts daily energy expenditure to encourage steady weight loss while preserving muscle mass.
A protein intake of 1.5 g/kg of body weight per day is recommended.
To optimize protein uptake, it's suggested that protein be distributed evenly across meals, aiming for 25-30 g per meal, inclusive of 2.5-2.8
g of leucine.
Participants will also receive a guidebook, crafted through the Delphi method, to facilitate the adoption of these dietary modifications in their daily routines.
Participants will receive an 8-week program consisting of exercise training.
It entails weekly group sessions, with each lasting an hour for 8 weeks.
These sessions, designed for groups of approximately 10, will blend resistance and aerobic workouts to enhance muscle mass and strength while reducing fat in individuals with SO.
Each session includes a 10-minute warm-up and cool-down, 20 minutes of resistance training using elastic bands, followed by a 20-minute brisk walking segment.
Participants will also receive a YouTube link and a pamphlet describing the exercises, encouraging them to maintain at least 30 minutes of exercise five times a week during and beyond the supervised programme.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Changes of muscle strength
Time Frame: Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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Handgrip strength (kg) will be measured by using the hand dynamometer.
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Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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Changes of muscle mass
Time Frame: Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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Muscle mass (kg) will be measured by using bioelectrical impedance analysis.
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Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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Changes of body mass index
Time Frame: Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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The weight and height will be combined to report BMI in kg/m^2.
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Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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Changes of waist circumference
Time Frame: Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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Waist circumference was taken as the minimum circumference between the umbilicus and xiphoid process and measured to the nearest 0.5 cm.
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Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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Changes of fat mass
Time Frame: Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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Fat mass (kg) will be measured by using bioelectrical impedance analysis.
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Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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The Short Physical Performance Battery (SPPB) scale
Time Frame: Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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The Short Physical Performance Battery (SPPB) scale will be used to measure physical function, which is a well-established tool for monitoring function in older people, which contains three kinds of assessments: stand for 10 seconds with feet in 3 different positions, 3-meter or 4-meter walking speed test, and time to rise from a chair for five times.
The scores of SPPB range from 0 (worst performance) to 12 (best performance).
The minimum and maximum values are 0 and 10 respectively.
Higher scores mean a better performance.
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Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Mini Nutritional Assessment (MNA) Short-form
Time Frame: Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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Participants' nutritional status will be assessed through the Mini Nutritional Assessment (MNA).
It is a simple and quick tool for assessing older people who are malnourished or at risk of malnutrition.
The MNA Short-form contains 6 items.
Questions are weighted, 2-3 points per item.
Scores are categorised as 0-7 (malnourished), 8-11 (at risk of malnutrition), 12-14 (normal nutritional status).
The minimum and maximum values are 0 and 14 respectively.
Higher scores mean a better nutritional status.
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Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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Health Action Process Approach (HAPA) Nutrition Self-efficacy Scale
Time Frame: Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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The nutrition self-efficacy scale is one part of the Health-Specific Self-efficacy Scale.
The nutritional self-efficacy scale is a 5-item scale, and each item is rated on 4-point likert scale from 1= very uncertain, 2=rather uncertain, 3=rather certain, 4=very certain.
Higher score means higher self-efficacy.
The minimum and maximum values are 0 and 20 respectively.
Higher scores mean a higher self-efficacy.
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Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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Dietary Quality Index-International (DQI-I)
Time Frame: Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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The DQI-I will be used to estimate the dietary quality of participants.
It is a well-used questionnaire without being affected by culture.
The total scores range from 0 to 100, with a higher score representing better diet quality.
The minimum and maximum values are 0 and 100 respectively.
Higher scores mean a better diet quality.
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Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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EuroQoL 5D (EQ-5D)
Time Frame: Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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The EQ-5D comprises five dimensions of health: mobility, self-care, usual activities, pain / discomfort, and anxiety/depression.
Each of them has three response categories: no, some, or extreme problems, and a 0-100 points visual analogue scale (EQ VAS).
The ratings from the five categories can be transformed into a utility index score by utilizing the scores derived from the preference weights of the general population in Hong Kong.
The utility score generally ranges from less than 0 to 1.
A higher score indicates higher health utility.
The EQ VAS ranges from 0 to 100, with higher scores indicate better imaginable health.
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Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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Diet Adherence
Time Frame: Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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The adherence to protein intake will be analyzed by a software program "Food Processor®".
If any participant forgets to keep the dietary record, the 7-day food recall method will be used by the experimental group facilitator to check the participant's food intake, an approach commonly used in nutritional studies.
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Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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Exercise Adherence
Time Frame: Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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Assessed based on the participants' self-reports on their overall adherence to the exercise regimen.
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Change from baseline to 8 weeks, 3 months, and 6 months after completing the program
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Collaborators and Investigators
Investigators
- Principal Investigator: Justina Liu, PhD, The Hong Kong Polytechnic University
Publications and helpful links
General Publications
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Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HSEARS20240214001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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