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Does Meal Replacement With a Carbohydrates and Protein Supplement Induce Weight Loss in Overweight and/or Obese Adults?

Not Applicable
Conditions
Weight Loss
Interventions
Behavioral: satiety
Registration Number
NCT04458493
Lead Sponsor
Western University, Canada
Brief Summary

Participants will be randomized into two groups, one group will be the control (no intervention at all) and the other will be CHO-PRO (meal replacement, Generation UCAN supplement, 400ml, 20% solution). Prior to the start of the experiment, all participants will be asked to record their satiety ratings, appetite and desire to eat (10-point visual analogue scale) 30, 60 and 120 minutes after their regular dinner for 3 days. On the first day of the experiment, all participants will be asked to measure their waist and hip circumferences, fasting blood glucose level, maximal number of pushups and body weight using a scale at home prior to breakfast. Instructions on how to do the measurements properly will be recorded in a video and distributed to the participants. Participants in the control group will not receive any intervention. Participants in the CHO-PRO group will be provided with the supplement and they will be asked to consume the CHO - protein supplement (Generation UCAN supplement, 250ml, 10% solution) 6 to 7 hours after lunch, in place of their dinner for 6 weeks. They will also be asked to record their satiety ratings, appetite and desire to eat (10-point visual analogue scale) 30, 60 and 120 minutes after each meal replacement drink. All participants will be required to complete a dietary record, prior to, and during (at weeks 2 and 4) intervention. To track adherence of the CHO-PRO group, participants will be asked to check off the calendar that they did not consume the meal replacement due to various reasons. On day 43, all participants will be asked measure again waist and hip circumferences, fasting blood glucose level, maximal number of pushups and body weight using a scale at home prior to breakfast again.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
50
Inclusion Criteria
  • sedentary (<2 moderate exercise bouts/wk)
  • between the ages of 18 to 40y
  • body mass index (BMI) between >25
Exclusion Criteria
  • do not eat three meals a day typically
  • taking medication that affects their eating patterns
  • have metabolic and gastrointestinal diseases

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
controlsatietyno supplement will be provided on the day of the experiment
Generation UCANsatietycarbohydrates - protein (Generation UCAN supplement, 400ml, 20% solution)
Primary Outcome Measures
NameTimeMethod
changes in body weight1 day prior to the start of the experiment and on the 31st day of the experiment

body weight will be measured using a scale at home prior to breakfast

Secondary Outcome Measures
NameTimeMethod
changes in fasted blood glucose1 day prior to the start of the experiment and on the 31st day of the experiment

blood glucose will be measured through finger pricks

changes in waist and hip circumferences1 day prior to the start of the experiment and on the 31st day of the experiment

waist and hip circumferences will be measured using a measuring tape at home prior to breakfast

changes in desire to eat ratings30, 60 and 120 minutes after each meal replacement drink

desire to eat ratings will be asked with the use a 10 point visual analog scale (VAS), 10 being no desire to eat at all and 1 being strong desire to eat

changes in appetite ratings30, 60 and 120 minutes after each meal replacement drink

appetite ratings will be asked with the use a 10 point visual analog scale (VAS), 10 being strong desire to consume food and 1 being no desire to consume food at all

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