Prosocial Behavior and Exercise Among Older Adults

Not Applicable

• Conditions: Health-Related Quality of Life; Physical Activity; Physical Function
• Interventions: Behavioral: Prosocial Behavior Physical Activity (PBPA); Behavioral: Physical Exercise (PE)

• Registration Number: NCT00747019
• Lead Sponsor: National Institute on Aging (NIA)

Brief Summary

The purpose of this study is to compare two exercise programs to determine how well they help older adults make exercise a regular habit after 9 months.

Detailed Description

Although only a small percentage of older adults engage in habitual physical activity, previous studies have demonstrated interventions that include cognitive-behavioral strategies can enhance long-term, independent physical activity. In addition, there are episodic charity events, such as charity walks, that attract large numbers of participants of all age ranges to engage in moderate-intensity physical activity. These actions are a form of prosocial behavior, defined as voluntary, intentional behavior that results in benefits for another. The opportunity to help others seems to be a motive in inspiring these individuals to at least engage in one session of moderate physical activity. Thus, the current research project contemplates whether prosocial behavior may be implemented as a viable behavioral incentive for long-term physical activity.

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.

Study Timeline

• Study First Submitted: 2008-09-03
• Study First Submitted QC: 2008-09-03
• Study First Posted: 2008-09-04
• Study Start: 2008-12
• Status Verified: 2009-06
• Last Update Submitted: 2009-06-30
• Last Update Posted: 2009-07-02
• Primary Completion: 2010-06
• Study Completion: 2010-06

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

• Between 55 and 80 years of age
• 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

• Self-reported evidence of cardiovascular disease risk, or documentation by the primary care physician of at least one of the following within the past 5 years:

  • 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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
PBPA	Prosocial Behavior Physical Activity (PBPA)	-
PE	Physical Exercise (PE)	-

Primary Outcome Measures

Name	Time	Method
Self-reported physical activity	Baseline, 3 and 9 months

Secondary Outcome Measures

Name	Time	Method
Physical function, health-related quality of life	Baseline, 3 and 9 months

Trial Locations

Locations (1)

Wake Forest University School of Medicine; 🇺🇸 Winston-Salem, North Carolina, United States