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A Mentor-Based Approach to Long-Term Weight Loss

This study has been completed.

Sponsors and Collaborators: University of Pittsburgh
National Institutes of Health (NIH)
Information provided by: University of Pittsburgh
ClinicalTrials.gov Identifier: NCT00177697
  Purpose

The purpose of this study to examine the effect of having a weight loss mentor on long-term weight loss in overweight adults.


Condition Intervention Phase
Weight Loss
Obesity
Behavioral: behavioral weight loss program
Phase I
Phase II

MedlinePlus related topics:   Obesity    Weight Control   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Open Label, Active Control, Single Group Assignment
Official Title:   A Mentor-Based Approach to Long-Term Weight Loss

Further study details as provided by University of Pittsburgh:

Primary Outcome Measures:
  • weight loss

Secondary Outcome Measures:
  • fitness
  • dietary intake
  • mediators

Estimated Enrollment:   174
Study Start Date:   September 1999
Estimated Study Completion Date:   July 2002

  Eligibility
Ages Eligible for Study:   21 Years to 55 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes

Criteria

Inclusion Criteria:

  1. Female
  2. 21-55 years of age
  3. BMI = 25-35 kg/m2
  4. Ability to provide informed consent.
  5. Ability to provide consent from their personal physician to participate in this study.

Exclusion Criteria:

  1. Reporting regular exercise participation of at least 20 minutes per day on at least 3 days per week during the previous six months. (This study is designed to recruit relatively sedentary adults.)
  2. Diabetes, hypothyroidism, or other medical conditions which would affect energy metabolism.
  3. Currently pregnant, pregnant within the previous six months, or planning on becoming pregnant within the next 12 months. (Pregnancy will be based on self-report and will be included on the detailed medical history that is completed by subjects.)
  4. Non-medicated resting systolic blood pressure >160 mmHg or non-medicated resting diastolic blood pressure >100 mmHg, or taking medication that would affect blood pressure.
  5. Taking medication that would affect resting heart rate or the heart rate response during exercise (e.g., beta blockade).
  6. Arrhythmia on resting or exercise electrocardiogram that would indicate that vigorous exercise was contraindicated.
  7. History of myocardial infarction or valvular disease.
  8. History of orthopedic complications that would prevent optimal participation in the exercise component (e.g., heel spurs, severe arthritis).
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00177697

Locations
United States, Pennsylvania
University of Pittsburgh    
      Pittsburgh, Pennsylvania, United States, 15203

Sponsors and Collaborators
University of Pittsburgh
National Institutes of Health (NIH)

Investigators
Principal Investigator:     John M Jakicic, Ph.D.     University of Pittsburgh    
  More Information


Study ID Numbers:   R01 DK58002
First Received:   September 13, 2005
Last Updated:   September 13, 2005
ClinicalTrials.gov Identifier:   NCT00177697
Health Authority:   United States: Institutional Review Board

Study placed in the following topic categories:
Body Weight
Signs and Symptoms
Obesity
Weight Loss
Body Weight Changes
Nutrition Disorders
Overweight
Overnutrition

ClinicalTrials.gov processed this record on October 23, 2008




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