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

W

Western University, Canada

Status

Unknown

Conditions

Weight Loss

Treatments

Dietary Supplement: Dietary Supplement: Generation UCAN supplementation
Behavioral: satiety

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

50 participants in 2 patient groups

control
Experimental group
Description:
no supplement will be provided on the day of the experiment
Treatment:
Behavioral: satiety
Generation UCAN
Experimental group
Description:
carbohydrates - protein (Generation UCAN supplement, 400ml, 20% solution)
Treatment:
Behavioral: satiety
Dietary Supplement: Dietary Supplement: Generation UCAN supplementation

Trial contacts and locations

0

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Central trial contact

Crystal Lee, BSc; Manuel Manuel, MSc

Data sourced from clinicaltrials.gov

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