Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
80 participants
INTERVENTIONAL
2008-12-31
2010-06-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Prosocial Behavior and Volunteerism to Promote Physical Activity in Older Adults
NCT01528761
Effects of Physical Activity on Cardiovascular Risk and Quality of Life
NCT02767739
Responses to Physical Activity Messages Among Midlife Adults
NCT04711512
Problem Solving/Physical Interventions and Aging
NCT00097643
A "Stand Up and Move More" Intervention for Older Adults
NCT03412084
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Both the Prosocial Behavior Physical Activity (PBPA) group and the Physical Exercise (PE) group will receive a cognitive-behavioral intervention to teach participants the behavioral skills necessary to engage in long-term (9-month) independent physical activity. Both programs will provide supervised exercise sessions so that participants learn how to safely and effectively engage in physical activity, and both programs will help participants set goals for activity and overcome barriers to exercise. However, in PBPA group, participants will be able to also earn boxes of food for donation to a charity based upon their physical activity.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
SINGLE_GROUP
PREVENTION
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
PBPA
Prosocial Behavior Physical Activity (PBPA)
The PBPA condition involves a center-based cognitive-behavioral intervention to teach participants the behavioral skills to engage in long-term (9-month) independent physical activity; delivered three times a week months 1-3; independent physical activity months 4-9. PBPA participants also earn boxes of food for donation to the Second Harvest Food Bank (SHFB) of Northwest North Carolina based upon their weekly physical activity.
PE
Physical Exercise (PE)
The PE condition is a center-based cognitive-behavioral intervention to teach participants the behavioral skills to engage in long-term (9-month) independent physical activity; delivered three times a week months 1-3; independent physical activity months 4-9.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Prosocial Behavior Physical Activity (PBPA)
The PBPA condition involves a center-based cognitive-behavioral intervention to teach participants the behavioral skills to engage in long-term (9-month) independent physical activity; delivered three times a week months 1-3; independent physical activity months 4-9. PBPA participants also earn boxes of food for donation to the Second Harvest Food Bank (SHFB) of Northwest North Carolina based upon their weekly physical activity.
Physical Exercise (PE)
The PE condition is a center-based cognitive-behavioral intervention to teach participants the behavioral skills to engage in long-term (9-month) independent physical activity; delivered three times a week months 1-3; independent physical activity months 4-9.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Physically underactive (moderate or vigorous physical activity for less than 2 days per week for the preceding 3 months)
* No evidence of any major psychological illness
* Written permission from the participant's primary care physician with specific certification of no severe risk of cardiovascular disease
* Participant resides within a 35-mile radius of the study site
* Participant will remain in the area for the duration of the study
Exclusion Criteria
* Myocardial infarction (MI)
* Percutaneous transluminal coronary angioplasty (PTCA)
* Chronic or unstable angina at rest or during physical exertion
* New York Heart Association (NYHA) Type I through Type IV congestive heart failure
* Unstable ventricular arrhythmias
* Cardiovascular surgery (coronary artery or valvular heart disease)
* Ischemic or hemorrhagic stroke
* Intermittent claudication during physical activity
* Edema in feet
* Self-reported or documented evidence of rheumatoid arthritis
* Self-reported or physician-reported evidence of current cigarette or cigar smoking
* Self-reported treatment for psychiatric illness within the past 5 years:
* Treatment for major depression or schizophrenia
* Currently receiving lithium or neuroleptics
* Hospitalization with the last 5 years for depression, or clinical judgment of treatment for major depression
* Hearing or sight impairments
* Cognitive impairment
* Alcohol consumption greater than 21 drinks per week, or self-reported alcoholism
* Inability to speak or read English
* Judgment of clinical staff
* Current participation in another medical intervention study
55 Years
80 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
National Institute on Aging (NIA)
NIH
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Division of Public Health Sciences, Wake Forest University School of Medicine
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Capri G. Foy, PhD, MS
Role: PRINCIPAL_INVESTIGATOR
Division of Public Health Sciences, Wake Forest University School of Medicine
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Wake Forest University School of Medicine
Winston-Salem, North Carolina, United States
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
References
Explore related publications, articles, or registry entries linked to this study.
Rejeski WJ, Brawley LR, Ambrosius WT, Brubaker PH, Focht BC, Foy CG, Fox LD. Older adults with chronic disease: benefits of group-mediated counseling in the promotion of physically active lifestyles. Health Psychol. 2003 Jul;22(4):414-23. doi: 10.1037/0278-6133.22.4.414.
Rejeski WJ, Foy CG, Brawley LR, Brubaker PH, Focht BC, Norris JL 3rd, Smith ML. Older adults in cardiac rehabilitation: a new strategy for enhancing physical function. Med Sci Sports Exerc. 2002 Nov;34(11):1705-13. doi: 10.1097/00005768-200211000-00003.
Eisenberg N, Miller PA. The relation of empathy to prosocial and related behaviors. Psychol Bull. 1987 Jan;101(1):91-119. No abstract available.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
AG0106
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.