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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03077295
Other study ID # 804
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 5, 2017
Est. completion date April 5, 2019

Study information

Verified date June 2019
Source University of Aberdeen
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This weight loss study will investigate the impact of diet composition and meal size (large breakfast meals and smaller evening meals) on body weight, energy balance and eating behaviour, by altering calorie (meal) distribution.


Description:

The aim of this study is to further strengthen our understanding of the role of dietary components (in particular fibre and protein) in a healthy diet. The information gained from this research will lead to better policy advice, particularly in relation to healthy weight management, metabolic control, mental health and intestinal health. It will also lay the foundations to produce healthier primary products and aid the food industry in developing new and healthier products (e.g. products that aid hunger control and satiety). This will be addressed through four interlinked objectives:

O1: Healthy weight management and improved metabolic and mental health O2: Identification of gut bacteria and compounds of relevance to vascular and gut health O3: Linking fibre consumption to intestinal microbial communities and health O4: Mathematical modelling of interactions between diet and gut microbial communities


Recruitment information / eligibility

Status Completed
Enrollment 19
Est. completion date April 5, 2019
Est. primary completion date April 5, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria:

- BMI ranging from 27-42 kg/m2;

- those habitually consuming breakfast (at least 5 times a week).

Exclusion Criteria:

- women who are pregnant, planning to be pregnant or breastfeeding

- subjects with food allergy

- diagnosis of diabetes, hypertension, renal, hepatic, haematological disease or coronary heart disease

- having given a pint of blood for transfusion purposes within the last month

- unsuitable veins for blood sampling

- inability to understand the participant information sheet

- inability to speak, read and understand the English language

- those on any prescription medications (other than oral contraceptives)

- those on any specific diet regimes

- those on any weight loss programmes (that may be affecting lifestyle, physical activity and diet).

Study Design


Related Conditions & MeSH terms


Intervention

Other:
High Fibre
High fibre/carbohydrate (50% CHO, 35% fat and 15% Protein) with 45% calories at breakfast and 20% evening meal provided and buffet lunch. Total dietary fibre will be at least 30g/d for 2000kcal intake and provided as a mixed soluble and insoluble fibre sources to maintain palatability of the diet (e.g. wheat bran, fava bean, lentil, buckwheat).
High Protein
• High protein diet (30% protein, 35% fat and 35% CHO) with 45% calories at breakfast and 20% evening meal provided and buffet lunch. Protein will be a mixed meat matrix to include poultry, fish, red meat, prawns, eggs, dairy. Total dietary fibre will be no more than 15g/d for 2000kcal intake.

Locations

Country Name City State
United Kingdom The Rowett Institute Aberdeen

Sponsors (1)

Lead Sponsor Collaborator
University of Aberdeen

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Energy Balance Chronic influence on energy balance (body weight, kg) measured up to day 71 of study
Secondary Acute effects on appetite after test meals Appetite questionnaires recorded on Visual Analogue Scales every 30mins on test days Baseline & week 4 of each treatment
Secondary Acute effects on biomarkers of health after test meals blood samples analysed for Glucose, Lipids and Hormones Baseline & week 4 of each treatment
Secondary Acute effects on gastric emptying after test meals gastric emptying (stable isotope, Octanoic acid labelled breath samples) Baseline & week 4 of each treatment
Secondary Resting Metabolic Rate (RMR) before & after test meals Chronic influence on metabolism or Thermic Effect of Food (TEF) using indirect calorimetry measurement Baseline & week 4 of each treatment
Secondary Faecal sample analysis for gut health Chronic influence on changes in gut microbiota up to 10 weeks
Secondary Bone Density Dual Energy X-ray Absorptiometry (DXA) Scan to measure fat mass, fat free mass & bone density as part of the 4 compartment model Baseline & week 4 of each treatment
Secondary Body Composition Air Displacement Plethysmography (BodPod) to measure body fat as part of the 4 compartment model Baseline & week 4 of each treatment
Secondary Total Body Water Deuterium Dilution to measure Total Body Water (TBW) as part of the 4 compartment model Baseline & week 4 of each treatment
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