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BEYOND Weight Loss Study (BEYOND)

Primary Purpose

Obesity

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Counterweight Plus
Sponsored by
NHS Greater Glasgow and Clyde
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity focused on measuring Weight loss

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • confirmation from general practitioner (GP) of suitability for intervention
  • written informed consent
  • female
  • BMI ≥30 kg/m2 and < 45kg/m2, weight<200 kg and <60 cm bore size

Exclusion Criteria:

  • known illness such as heart disease, cancer, or any disability that would affect weight loss (diabetes not an exclusion) or prevent completion of the intervention
  • implanted electronic devices that are MRI incompatible or MRI unsafe, ferromagnetic foreign bodies
  • substance abuse
  • myocardial infarction within previous 6 months
  • learning difficulties and subjects having difficulty in understanding verbal or written English
  • pregnant/ considering pregnancy
  • patients who have required hospitalisation for depression or are on antipsychotic drugs
  • people currently participating in another clinical research trial
  • recent weight loss >5kg within the last 6 months
  • current treatment with anti-obesity drugs
  • diagnosed eating disorder

Sites / Locations

  • Glasgow Royal Infirmary

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Counterweight Plus Dietary Intervention

Arm Description

Weight management programme including total diet replacement with soups and shakes; approximately 800 calories/day

Outcomes

Primary Outcome Measures

WP1: change in body composition with substantial, non-surgical, weight loss
Measurement of muscle mass before and after a weight loss programme using MRI
WP1: change in body composition with substantial, non-surgical, weight loss
Measurement of fat mass before and after a weight loss programme using MRI
WP2: metabolic adaptation during weight loss and maintenance
Change in resting metabolic rate before and after weight loss
WP3: weight regain prevention
% achieving >15kg weight loss at 12 and 24 months

Secondary Outcome Measures

Muscle/fat mass of specific muscle groups
Relationship between predicted muscle and fat mass with the strength of specific muscle groups (by muscle strength, gait analysis and WOMAC questionnaire)
Adherence and acceptability of Rescue Packages to Patients
Number of participants requiring and completing rescue packages
Metabolic adaptive effect of weight loss
Comparison of leptin, ghrelin and thyroid hormone levels at baseline to those during weight loss and maintenance to establish
Weight regain prevention
changes in BED Questionnaire Rating Score
Weight regain prevention
% undertaking Rescue Package during Weight Loss Maintenance
Weight regain prevention
rate of weight regain during Weight Loss Maintenance

Full Information

First Posted
December 19, 2014
Last Updated
January 17, 2018
Sponsor
NHS Greater Glasgow and Clyde
Collaborators
University of Glasgow
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1. Study Identification

Unique Protocol Identification Number
NCT02340793
Brief Title
BEYOND Weight Loss Study
Acronym
BEYOND
Official Title
Body Composition and Energy Expenditure With Total Diet Replacement During Weight Loss and Maintenance
Study Type
Interventional

2. Study Status

Record Verification Date
January 2018
Overall Recruitment Status
Completed
Study Start Date
January 2015 (undefined)
Primary Completion Date
February 2017 (Actual)
Study Completion Date
February 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
NHS Greater Glasgow and Clyde
Collaborators
University of Glasgow

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
National guidelines recommend 15-20% weight loss for severe and complicated obesity. Weight loss maintenance can be achieved in around 33% of patients at 12 months. The BEYOND study will administer Counterweight Plus; a nutritionally replete Total Diet Replacement Plan (TDR) of 800+ Calories followed by structured Food Reintroduction, and Weight Loss Maintenance programmes. The study will incorporate three work packages with the aim of: examining changes in body composition with substantial (target >15kg) non-surgical weight loss (work package 1, WP1) characterizing the metabolic adaptations during weight loss and maintenance (work package 2, WP2) examining Rescue Packages as a method of weight re-gain prevention (work package 3, WP3).
Detailed Description
All participants will receive the Counterweight Plus dietary intervention. This consists of: 12-20 weeks 800+ calories/day Total Diet Replacement Plan, followed by 6-8 weeks Food Reintroduction, followed by up to 104 weeks Weight Loss Maintenance, based on maintaining daily calorie restriction. All participants will undergo the following investigations at baseline and at regular intervals throughout the study period: height (baseline only) whole body MRI scans: total-body skeletal muscle volume and fat mass will be measured using whole-body multi-slice MRI (baseline and 12 weeks only) functional assessment: completion of the Western Ontario and McMaster Universities Arthritis Index (WOMAC) (baseline and 12 weeks only) gait and muscle strength assessment: biomechanical gait analysis will be carried out using an 8 camera VICON system during flat walking to determine maximum flexion and extension moments for both limbs and maximum adduction and abduction moments. Muscle strength will also be directly measured of both the upper (grip strength) and lower (quadriceps and hamstrings) limb using a dynamometer and myometer (baseline and 12 weeks only) anthropometric measurement: body weight; waist, hip, thigh, arm and calf circumferences indirect calorimetry: resting metabolic rate will be measured by a computerised open-circuit ventilated hood system fasting blood sampling: for measurement of HbA1C, lipid profile, leptin, thyroid hormones gut microbiota analysis from faecal samples Binge Eating Disorder and Quality of Life (EQ-5D) questionnaires Participants will receive regular support/advice from a research dietician/ nutritionist during the two year study period.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity
Keywords
Weight loss

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
23 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Counterweight Plus Dietary Intervention
Arm Type
Experimental
Arm Description
Weight management programme including total diet replacement with soups and shakes; approximately 800 calories/day
Intervention Type
Dietary Supplement
Intervention Name(s)
Counterweight Plus
Intervention Description
A non-surgical, nutritionally replete weight management programme comprising a Total Diet Replacement Plan (TDR) of 800+ calories/day to produce a weight loss of >15kg over 12-20 weeks; followed by a structured Food Reintroduction phase for 6-8 weeks and a Weight Loss Maintenance phase; total intervention period 2 years.
Primary Outcome Measure Information:
Title
WP1: change in body composition with substantial, non-surgical, weight loss
Description
Measurement of muscle mass before and after a weight loss programme using MRI
Time Frame
20 weeks
Title
WP1: change in body composition with substantial, non-surgical, weight loss
Description
Measurement of fat mass before and after a weight loss programme using MRI
Time Frame
20 weeks
Title
WP2: metabolic adaptation during weight loss and maintenance
Description
Change in resting metabolic rate before and after weight loss
Time Frame
2 years
Title
WP3: weight regain prevention
Description
% achieving >15kg weight loss at 12 and 24 months
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Muscle/fat mass of specific muscle groups
Description
Relationship between predicted muscle and fat mass with the strength of specific muscle groups (by muscle strength, gait analysis and WOMAC questionnaire)
Time Frame
20 weeks
Title
Adherence and acceptability of Rescue Packages to Patients
Description
Number of participants requiring and completing rescue packages
Time Frame
2 years
Title
Metabolic adaptive effect of weight loss
Description
Comparison of leptin, ghrelin and thyroid hormone levels at baseline to those during weight loss and maintenance to establish
Time Frame
2 years
Title
Weight regain prevention
Description
changes in BED Questionnaire Rating Score
Time Frame
2 years
Title
Weight regain prevention
Description
% undertaking Rescue Package during Weight Loss Maintenance
Time Frame
2 years
Title
Weight regain prevention
Description
rate of weight regain during Weight Loss Maintenance
Time Frame
2 years

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: confirmation from general practitioner (GP) of suitability for intervention written informed consent female BMI ≥30 kg/m2 and < 45kg/m2, weight<200 kg and <60 cm bore size Exclusion Criteria: known illness such as heart disease, cancer, or any disability that would affect weight loss (diabetes not an exclusion) or prevent completion of the intervention implanted electronic devices that are MRI incompatible or MRI unsafe, ferromagnetic foreign bodies substance abuse myocardial infarction within previous 6 months learning difficulties and subjects having difficulty in understanding verbal or written English pregnant/ considering pregnancy patients who have required hospitalisation for depression or are on antipsychotic drugs people currently participating in another clinical research trial recent weight loss >5kg within the last 6 months current treatment with anti-obesity drugs diagnosed eating disorder
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael EJ Lean, MA MB BChir MD
Organizational Affiliation
University of Glasgow
Official's Role
Principal Investigator
Facility Information:
Facility Name
Glasgow Royal Infirmary
City
Glasgow
State/Province
Scotland
ZIP/Postal Code
G31 2ER
Country
United Kingdom

12. IPD Sharing Statement

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