Status:

UNKNOWN

Prosocial Behavior and Exercise Among Older Adults

Lead Sponsor:

National Institute on Aging (NIA)

Conditions:

Health-Related Quality of Life

Physical Activity

Eligibility:

All Genders

55-80 years

Phase:

NA

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-te...

Eligibility Criteria

Inclusion

  • 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

  • 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

Key Trial Info

Start Date :

December 1 2008

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

June 1 2010

Estimated Enrollment :

80 Patients enrolled

Trial Details

Trial ID

NCT00747019

Start Date

December 1 2008

End Date

June 1 2010

Last Update

July 2 2009

Active Locations (1)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 1 (1 locations)

1

Wake Forest University School of Medicine

Winston-Salem, North Carolina, United States, 27127