ClinicalTrials.gov
 Home    Search    Study Topics    Glossary  
 

  Full Text View  
  Tabular View  
  Contacts and Locations  
  No Study Results Posted  
  Related Studies  
Effect of Exercise on Prevention of Weight Gain

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: NCT00177502
  Purpose

The purpose of this study is to examine the dose-response of exercise on prevention of weight gain in overweight adults.


Condition Intervention Phase
Weight Loss
Behavioral: behavioral exercise intervention
Phase I
Phase II

MedlinePlus related topics:   Exercise and Physical Fitness    Weight Control   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Prevention, Randomized, Open Label, Active Control, Single Group Assignment
Official Title:   Effect of Exercise on Prevention of Weight Gain

Further study details as provided by University of Pittsburgh:

Primary Outcome Measures:
  • body weight

Secondary Outcome Measures:
  • fitness
  • physical activity
  • dietary intake
  • mediators

Estimated Enrollment:   294
Study Start Date:   January 2003
Estimated Study Completion Date:   December 2006

  Eligibility
Ages Eligible for Study:   18 Years to 55 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes

Criteria

Inclusion Criteria:

  1. Female or Male
  2. 18-55 years of age
  3. BMI = 25-29.9 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. Women who are currently pregnant, pregnant within the previous six months, or planning on becoming pregnant within the next 12 months. (Pregnancy during initial screening will be based on self-report and will be included on the detailed medical history that is completed by subjects. However, this will be confirmed with the urine pregnancy test that will be conducted prior to the baseline DEXA.)
  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: NCT00177502

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 HL070257-01A1, R01 HL070257-01A1
First Received:   September 12, 2005
Last Updated:   September 12, 2005
ClinicalTrials.gov Identifier:   NCT00177502
Health Authority:   United States: Institutional Review Board

Study placed in the following topic categories:
Body Weight
Signs and Symptoms
Weight Loss
Body Weight Changes
Weight Gain

ClinicalTrials.gov processed this record on October 23, 2008




Links to all studies - primarily for crawlers