Weight Loss Interventions for Obesity

Sponsor
National University Hospital, Singapore (Other)
Overall Status
Recruiting
CT.gov ID
NCT06022796
Collaborator
(none)
50
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2
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Study Details

Study Description

Brief Summary

Numerous barriers towards weight management among Singaporeans with obesity exists, which involves environmental and self-regulation factors (i.e. motivation and hunger). Hence, the provision of healthy ketogenic ready-to-eat meals may be a potential solution to facilitate initial weight loss through increasing motivation while reducing appetite and hunger levels among these individuals. Therefore, this study will investigate the effect of healthy ketogenic ready-to-eat meals with mHealth nutrition application versus healthy ketogenic diet (without meal provision) with the mHealth nutrition app to facilitate weight loss and improve metabolic outcomes among individuals with obesity.

Condition or Disease Intervention/Treatment Phase
  • Other: Healthy Ketogenic Ready-to-Eat Meals
  • Other: Healthy Ketogenic Diet
N/A

Detailed Description

In Singapore, the widespread availability of local meals and concerns of overconsumption due to a lack of internal self-regulation skills for hunger predisposes an increased energy intake. Furthermore, a lack of time, motivation, and self-efficacy in preparing healthy meals may potentially limit the extent of weight and dietary management among local individuals with obesity.

The ketogenic diet has consistently demonstrated beneficial effects on facilitating weight management. This weight loss mechanism involves achieving a calorie deficit, induced state of nutritional ketosis, and the reduction in appetite and hunger. Importantly, the weight loss achieved from the early phase of the intervention serves as one of the key enablers in the weight loss process. Despite these benefits, there is paucity in the literature examining the provision of healthy ketogenic ready-to-eat (HK-RTE) meals on weight loss. Furthermore, none of these studies explored the extent of motivation derived from the benefits of these meals, nor included the use of mHealth self-monitoring strategies to encourage weight loss.

To address the research gap, our study aims to evaluate the effectiveness of HK-RTE meals with mHealth app, as compared to healthy ketogenic diet (HKD) (without meal provision) using the mHealth app on weight loss and metabolic outcomes among Asian individuals with obesity.

In this randomized controlled trial, participants will be randomized to either HK-RTE group or the HKD group using computer-generated random sequencing. Both groups will receive nutrition education conducted by dietitians throughout the 6-month study period (total of 5 dietary workshops covering topics such as ketogenic dietary advice and self-monitoring habits).

The HK-RTE group will be provided with HK-RTE meals for lunch and dinner in the first month (n = 25). They are to take these meals as part of a healthy ketogenic diet, with a maximum of 50g net total carbohydrates daily. Those in the control group will be advised to follow a healthy ketogenic diet (HKD) without the RTE meals (n = 25) and similarly to keep to a maximum of 50g net carbohydrates daily. Participants will also be encouraged to use the Nutritionist Buddy (nBuddy) mobile application to facilitate monitoring of diet intake, physical activity and weight throughout the 6-month study period. The impact of the HK-RTE meals on motivation and appetite regulation in influencing weight loss will also be explored.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
In this randomized controlled trial, participants in the HK-RTE group will be advised to follow a healthy ketogenic diet with RTE meals provided (n=25), with a maximum of 50g net carbohydrate intake daily. Those in the control group will be instructed to follow a healthy ketogenic diet (HKD) (n=25).In this randomized controlled trial, participants in the HK-RTE group will be advised to follow a healthy ketogenic diet with RTE meals provided (n=25), with a maximum of 50g net carbohydrate intake daily. Those in the control group will be instructed to follow a healthy ketogenic diet (HKD) (n=25).
Masking:
None (Open Label)
Masking Description:
It is not feasible to apply blinding to the study design due to the nature of the intervention
Primary Purpose:
Treatment
Official Title:
Weight Loss Interventions for Obesity
Actual Study Start Date :
Jul 21, 2023
Anticipated Primary Completion Date :
Mar 1, 2024
Anticipated Study Completion Date :
May 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Healthy Ketogenic Ready-To-Eat (HK-RTE) Meals

Participants in the HK-RTE group (n=25) will be provided with the Healthfull meals for lunch and dinner in the first month. They will be advised to take these meals as part of a healthy ketogenic diet, with a maximum of 50g total net carbohydrates daily. Participants will receive nutrition education conducted by dietitians over the course of 6 months (total of 5 dietary workshops covering topics such as ketogenic dietary advice and self-monitoring habits). Participants will also receive health coaching via the Nutritionist Buddy (nBuddy) mobile application to facilitate monitoring of diet intake, physical activity and weight throughout the 6 months study period.

Other: Healthy Ketogenic Ready-to-Eat Meals
Participants will be provided nutrition education via 5 dietary workshops focusing on a healthy ketogenic diet. In addition, HK-RTE meals will be provided to participants as a form of meal replacement for lunch and dinner over 1 month. Participants will be expected to follow a healthy ketogenic diet thereafter.
Other Names:
  • Very low carbohydrate diet
  • Active Comparator: Healthy Ketogenic Diet (HKD)

    Participants in the reference group will be instructed to follow a Healthy Ketogenic Diet (n = 25), with a maximum of 50g total net carbohydrates daily. Similar to the experimental group, participants will receive nutrition education conducted by dietitians over the course of 6 months (total of 5 dietary workshops such as ketogenic dietary advice and self-monitoring habit). Participants will also receive health coaching via the Nutritionist Buddy (nBuddy) mobile application to facilitate monitoring of diet intake, physical activity and weight throughout the 6 months study period.

    Other: Healthy Ketogenic Diet
    Participants will receive nutrition education via 5 dietary workshops focusing on a healthy ketogenic diet, without the provision of HK-RTE meals.

    Outcome Measures

    Primary Outcome Measures

    1. Body weight [1 month, 3 months, 6 months]

      Weight changes post-intervention

    Secondary Outcome Measures

    1. Blood pressure [3 months, 6 months]

      Systolic and diastolic changes at follow up appointments

    2. Hemoglobin A1c [3 months, 6 months]

      HbA1c changes at follow up appointments

    3. Fasting blood glucose [3 months, 6 months]

      Fasting blood glucose changes at follow up appointments

    4. Total cholesterol [3 months, 6 months]

      Cholesterol changes at follow up appointments

    5. Low-density lipoprotein cholesterol [3 months, 6 months]

      Cholesterol changes at follow up appointments

    6. High-density lipoprotein cholesterol [3 months, 6 months]

      Cholesterol changes at follow-up appointments

    7. Triglycerides [3 months, 6 months]

      Triglycerides changes at follow up appointments

    8. Motivation to initiate and maintain dietary behaviours [3 months, 6 months]

      Motivation via self-reported questionnaire

    9. Perceived competence to maintain dietary behaviour [3 months, 6 months]

      Perceived competence via self-reported questionnaire

    10. Hunger [3 months, 6 months]

      Subjective ratings of hunger feelings via self-reported questionnaire

    11. Dietary intake [6 months]

      Nutrients intake by assessing food logs in nBuddy application

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    21 Years to 75 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Aged 21 to 75 years old

    • Body Mass Index >= 27.5kg/m2

    • Own a smartphone

    • Literacy in English

    • NUH staff

    Exclusion Criteria:
    • Intention of pregnancy; Pregnancy; Lactating individuals

    • Type 1 Diabetes Mellitus or Type 2 Diabetes Mellitus on insulin treatment

    • Untreated Endocrinopathy (e.g., hyper/hypothyroidism)

    • Advanced kidney disease

    • Abnormal liver function test assessed at screening

    • Heart diseases

    • Severe cognitive or psychiatric disabilities/disorders (e.g., eating disorders, depression)

    • Active malignancies

    • Taking medications that affect appetite or induce weight loss; previous or plans for bariatric surgery.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 National University Hospital Singapore Singapore 119074

    Sponsors and Collaborators

    • National University Hospital, Singapore

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    National University Hospital, Singapore
    ClinicalTrials.gov Identifier:
    NCT06022796
    Other Study ID Numbers:
    • 202300165
    First Posted:
    Sep 5, 2023
    Last Update Posted:
    Sep 5, 2023
    Last Verified:
    Aug 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 5, 2023