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OpenTrials
Completed

NCT Number: NCT00177632

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

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.

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Key information

Age range

25 year–55 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

University of Pittsburgh

Pittsburgh, Pennsylvania, 15203, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female
  • 25-55 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

  • 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.)
  • Currently being treated for psychological disorders/conditions and/or currently taking psychotropic medication.
  • Diabetes, hypothyroidism, or other medical conditions which would affect energy metabolism.
  • 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).
  • 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).

Treatment and study plan

Behavioral weight loss

Behavioral

Primary outcomes

  1. weight loss

Secondary outcomes

  1. fitness

  2. physical activity

  3. dietary intake

  4. mediators

Sponsors and collaborators

Lead sponsor

University of Pittsburgh

Other

Registry information

Important dates

Study start
2003
Study completion
2004
First posted
Sep 15, 2005
Registry last updated
Sep 15, 2005

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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