Evaluation of Alternative Exercise Treatments on Weight Loss in Overweight Women.

Phase 1

Completed

• Conditions: Obesity; Weight Loss

• Registration Number: NCT00177632
• Lead Sponsor: University of Pittsburgh

Brief Summary

The purpose is to examine the additional effect of either yoga or resistance exercise on weight loss weight combined with a standard behavioral weight loss intervention.

Detailed Description

Not available

Study Timeline

• Study Start: 2003-07
• Study Completion: 2004-07
• Status Verified: 2005-09
• Study First Submitted: 2005-09-13
• Study First Submitted QC: 2005-09-13
• Last Update Submitted: 2005-09-13
• Study First Posted: 2005-09-15
• Last Update Posted: 2005-09-15

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 66

Inclusion Criteria

1. Female
2. 25-55 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. Participation in regular exercise (aerobic, yoga or resistance exercise) for > 20 minutes per day on > 2 days per week for the last 3 months. (This study is designed to recruit relatively sedentary adults.)
2. Currently being treated for psychological disorders/conditions and/or currently taking psychotropic medication.
3. Diabetes, hypothyroidism, or other medical conditions which would affect energy metabolism.
4. 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, pregnancy status will also be verified by the pregnancy test that is required for the baseline, 6 and 12 month DEXA).
5. 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.
6. Taking medication that would affect resting heart rate or the heart rate response during exercise (e.g., beta blockade).
7. Arrhythmia on resting or exercise electrocardiogram that would indicate that vigorous exercise was contraindicated.
8. History of myocardial infarction or valvular disease.
9. History of orthopedic complications that would prevent optimal participation in the exercise component (e.g., heel spurs, severe arthritis).

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
weight loss

Secondary Outcome Measures

Name	Time	Method
mediators
fitness
physical activity
dietary intake

Trial Locations

Locations (1)

University of Pittsburgh; 🇺🇸 Pittsburgh, Pennsylvania, United States