Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
FEMALE
Healthy Volunteers
ID07299942

Beta-glucan Supplementation During Calorie and Carbohydrate-restricted Diet: Impact on Body Weight and Body Fat Loss, Subjective Appetite, and Gastrointestinal Appetite Hormones of Healthy Women With Overweight.

Led by University of Glasgow · Updated on 2025-12-23

60

Participants Needed

1

Research Sites

47 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate whether adding beta-glucan supplements to a calorie- and carbohydrate-restricted diet helps women with overweight or obesity lose body weight and fat, while also reducing negative changes in appetite and related hormones. The trial is a double-blind, randomized, controlled study involving healthy females aged 18 to 60 with a BMI between 25 and 39.9. It compares beta-glucan to a placebo (cellulose) to understand its effects during dietary restriction. Participants will be randomly assigned to one of two groups: one receiving 9 grams per day of beta-glucan and the other receiving 9 grams per day of cellulose as a placebo. Both groups will follow a 4-week diet with low-calorie liquid meal replacements for breakfast and dinner, each providing 200 kcal, and low-carbohydrate lunches making up 35% of habitual energy intake. Supplements are taken with each main meal, and participants receive support and monitoring during the intervention. Before and after the 4-week intervention, participants undergo experimental trials involving fasting body weight and composition measurements, saliva collection to assess body water, and blood sampling over 4 hours to measure appetite hormones. Subjective appetite is recorded using questionnaires. Participants also track their food and drink intake for three days before each trial day. The study measures body weight, total body water, subjective appetite, and gastrointestinal appetite hormones to assess the intervention's impact.

CONDITIONS

Brief Title

Impact of Beta-glucan Supplementation During Calorie and Carbohydrate-restricted Diet on Body Weight and Body Fat Loss, Appetite, and Gastrointestinal Appetite Hormones.

Who Can Participate

Age: 18Years - 60Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthy females living with overweight or obese (BMI of 25 - 39.9 kg/m2).
  • Age between 18 to 60 years.
  • Stable body weight for at least 3 months preceding the study.
Not Eligible

You will not qualify if you...

  • Smokers
  • Irregular menstrual cycle
  • Exercising more than 75 minutes a week
  • Pregnant or lactating
  • Food allergies
  • Vegan or vegetarian or follow any diet other than the typical Western diet.
  • Taking dietary supplement at the time of the study.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Experimental Trial (Pre-intervention)

Duration - 1 day

Participants complete baseline measurements including body weight, subjective appetite questionnaire, blood and saliva samples, and consume a standardized low-calorie breakfast with the assigned supplement.

1 visit (in-person)

Treatment

Duration - 4 weeks

Participants follow a 4-week calorie and carbohydrate-restricted diet combined with daily beta-glucan or placebo supplementation taken with each main meal. Weekly dietary support is provided via telephone or email.

Weekly contacts and daily supplement intake

Experimental Trial (Post-intervention)

Duration - 1 day

Participants repeat the experimental trial to assess changes in body composition, subjective appetite, and gastrointestinal hormones after the intervention.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

Human Nutrition, College of Medicine, Veterinary and Life Science,

Glasgow, United Kingdom, G31 2ER

Actively Recruiting

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Research Team

D

Dalia Malkova

N

Nesreen Baobid

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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