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The Effectiveness of Commercial Weight Loss Programmes

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ClinicalTrials.gov Identifier: NCT00327821
Recruitment Status : Completed
First Posted : May 19, 2006
Last Update Posted : July 21, 2006
Sponsor:
Collaborator:
British Broadcasting Corporation
Information provided by:
University of Surrey

Brief Summary:

The objective is to compare the effectiveness of 4 different commercial weight-loss diets available to adults in the UK.

This is achieved with a 6 month multi-centre randomised unblinded controlled trial of

  • Dr Atkins' New Diet Revolution,
  • The slimFast Plan,
  • The weight Watchers Pure Points Programme,
  • Rosemary Conley's "Eat Yourself Slim" Diet & Fitness Plan.
  • No diet (control)

Subjects are a community based sample of 300 (60 per group) otherwise healthy overweight and obese adults.

Main outcome measures are weight and body fat change over 6 months.


Condition or disease Intervention/treatment Phase
Obesity Behavioral: calorie controlled diet Not Applicable

Study Type : Interventional  (Clinical Trial)
Enrollment : 300 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Official Title: A Randomised Control Trial of Commercial Weight Loss Programme in a Community Based Sample of Obese Adults.
Study Start Date : July 2002
Study Completion Date : March 2003

Resource links provided by the National Library of Medicine

U.S. FDA Resources




Primary Outcome Measures :
  1. Weight loss
  2. Fat loss


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Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Body mass index (BMI) > 27 and < 40 kg/m2.

Exclusion Criteria:

  • History of coronary heart disease
  • Type 1 or Type 2 diabetes
  • Renal, liver or respiratory failure
  • Gout
  • Taking lipid lowering or anti-hypertensive drugs
  • History of obesity with known cause (i.e. Cushings disease, hypothyroidism)
  • Previous gastric or weight loss surgery
  • Taking any weight loss drug (including Orlistat or Sibutramine)
  • Clinical depression
  • Eating disorders
  • Drug or alcohol abuse
  • Any malabsorptive state (including lactose intolerance)
  • Being treated for a malignancy
  • Being pregnant
  • Breastfeeding

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00327821


Locations
United Kingdom
University of Surrey
Guildford, Surrey, United Kingdom, GU2 7XH
Sponsors and Collaborators
University of Surrey
British Broadcasting Corporation
Investigators
Principal Investigator: D J Millward, PhD University of Surrey
Study Director: H A Truby, PhD SRD University of Surrey