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Sponsors and Collaborators: |
National Heart, Lung, and Blood Institute (NHLBI) Thomas Jefferson University |
Information provided by: | National Heart, Lung, and Blood Institute (NHLBI) |
ClinicalTrials.gov Identifier: | NCT00242658 |
This study will test the efficacy of providing primary care physicians and their patients with computer-tailored information, based on patients’ responses to survey questions. The health education messages are designed to encourage patients to become physically active and to encourage physicians to counsel their patients about exercise.
Condition | Intervention | Phase |
Hypertension |
Behavioral: Physical Activity Behavioral: Health Education Behavioral: Health Promotion Behavioral: Comparative Analysis Behavioral: Blood Pressure Control |
Phase I |
MedlinePlus related topics: | High Blood Pressure |
Study Type: | Interventional |
Study Design: | Educational/Counseling/Training, Randomized, Single Blind, Active Control, Parallel Assignment, Efficacy Study |
Official Title: | Computerized Physical Activity Promotion in Primary Care |
Estimated Enrollment: | 394 |
Study Start Date: | May 2005 |
The main objective of this study is to determine, via a 6-month randomized controlled study, the efficacy of providing tailored physical activity computer reports to patients and physicians. The primary outcome will be minutes of physical activity of at least moderate intensity, assessed after a 3-month intervention and subsequent 3 months of follow-up. This study will examine the effect of the intervention on fitness, measured as V02 peak, which is the maximum amount of oxygen consumption a person can achieve. This study will examine potential mediators of physical activity participation, with particular attention to the effect of health outcome expectations for exercise as a potential mediator of exercise adoption. Another objective of the study is to test methods to improve blood pressure control and preventive service utilization.
Ages Eligible for Study: | 21 Years to 65 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Exclusion Criteria:
United States, Pennsylvania | |||||
Jefferson Medical College, Department of Health Policy | |||||
Philadelphia, Pennsylvania, United States, 19107 | |||||
Jefferson Family Medicine Associates | |||||
Philadelphia, Pennsylvania, United States, 19107 |
National Heart, Lung, and Blood Institute (NHLBI) |
Thomas Jefferson University |
Study Chair: | Christopher N. Sciamanna, MD, MPH | Jefferson Medical College, Department of Health Policy |
Click here for the Principal Investigator's CV and departmental web site 
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Study ID Numbers: | 269, 7 R01 HL067005-03, 02F.214 CHIP |
First Received: | October 19, 2005 |
Last Updated: | October 12, 2006 |
ClinicalTrials.gov Identifier: | NCT00242658 |
Health Authority: | United States: Federal Government |
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