NCT Number: NCT00177476
Enhancing Exercise Participation in Overweight Adults
The purpose of this study is to examine whether behavioral strategies implemented during the adoption versus the maintenance periods of weight loss to enhance exercise participation in overweight adults are more effective than a standard behavioral intervention.
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Conditions
Age range
18 year–55 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 1 / Phase 2
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Female or Male
- 18-55 years of age
- BMI = 25-39.9 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.
- Women who are currently pregnant, pregnant within the previous six months, or planning on becoming pregnant within the next 18 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)
- 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.
- Weight loss of >5% of body weight within the previous 12 months.
- History of orthopedic complications that would prevent optimal participation in the exercise component (e.g., heel spurs, severe arthritis).
Treatment and study plan
Primary outcomes
-
body weight
Secondary outcomes
-
Fitness
-
physical activity
-
dietary intake
-
mediators
Sponsors and collaborators
Lead sponsor
University of Pittsburgh
Other
Collaborators
- National Institutes of Health (NIH)
Registry information
Important dates
- Study start
- 2003
- Study completion
- 2006
- 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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