A Mentor-Based Approach to Long-Term Weight Loss
This study has been completed.
Sponsor:
University of Pittsburgh
Collaborator:
Information provided by:
University of Pittsburgh
ClinicalTrials.gov Identifier:
NCT00177697
First received: September 13, 2005
Last updated: NA
Last verified: September 2005
History: No changes posted
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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 1 Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A Mentor-Based Approach to Long-Term Weight Loss |
Resource links provided by NLM:
Further study details as provided by University of Pittsburgh:
Eligibility| Ages Eligible for Study: | 21 Years to 55 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- Female
- 21-55 years of age
- BMI = 25-35 kg/m2
- Ability to provide informed consent.
- Ability to provide consent from their personal physician to participate in this study.
Exclusion Criteria:
- 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.)
- Diabetes, hypothyroidism, or other medical conditions which would affect energy metabolism.
- 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.)
- 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.
- Taking medication that would affect resting heart rate or the heart rate response during exercise (e.g., beta blockade).
- Arrhythmia on resting or exercise electrocardiogram that would indicate that vigorous exercise was contraindicated.
- History of myocardial infarction or valvular disease.
- 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
Investigators
| Principal Investigator: | John M Jakicic, Ph.D. | University of Pittsburgh |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00177697 History of Changes |
| Other Study ID Numbers: | R01 DK58002 |
| Study First Received: | September 13, 2005 |
| Last Updated: | September 13, 2005 |
| Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
|
Obesity Weight Loss Overnutrition Nutrition Disorders |
Overweight Body Weight Signs and Symptoms Body Weight Changes |
ClinicalTrials.gov processed this record on May 19, 2013