An Intervention to Increase Physical Activity Among African American Women

This study has been completed.
Sponsor:
Information provided by:
National Institute on Aging (NIA)
ClinicalTrials.gov Identifier:
NCT00473044
First received: May 10, 2007
Last updated: December 29, 2008
Last verified: December 2008
  Purpose

The purpose of this study is to investigate whether a faith-based curriculum delivered in small groups, and emphasizing goal setting along with mutual responsibility, increases physical activity.


Condition Intervention
Sedentary Lifestyle
Inactivity
Behavioral: Sisters in Motion

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind
Primary Purpose: Treatment
Official Title: An Intervention to Increase Physical Activity Among African American Women

Further study details as provided by National Institute on Aging (NIA):

Primary Outcome Measures:
  • Change in weekly steps walked as measured by pedometer [ Time Frame: 10 weeks and 6 months ]

Secondary Outcome Measures:
  • Change in weekly metabolic equivalents expended in physical activity [ Time Frame: 10 weeks and 6 months ]
  • Change in blood pressure, weight, and low-density lipoprotein (LDL) cholesterol [ Time Frame: 10 weeks and 6 months ]

Estimated Enrollment: 104
Study Start Date: April 2006
Study Completion Date: January 2008
Primary Completion Date: January 2008 (Final data collection date for primary outcome measure)
Detailed Description:

Sedentary lifestyles are common among older adults in the United States, especially among minority women. Regular physical activity in older adults has been shown to prevent falls, maintain functional status, prevent both dementia and osteoporosis, and decrease mortality. A review of the literature has shown that current research approaches using exercise classes as the only means of behavior change are ineffective and do not produce long-term sustainable improvement. This study is testing a culturally appropriate behavior modification intervention using 1) group prayer, 2) the development of social support and mutual responsibility for exercise, and 3) group problem solving activities to increase aerobic and strength-related activities among older African American women.

Participants randomized into the intervention arm receive a 45-minute curriculum session and a 45 minute exercise class, while those randomized into the control arm receive a 45 minute session of interactive lectures on unrelated health topics along with the 45 minute exercise class. The exercise class includes both aerobic exercise and strength training using hand-held weights.

Data is collected from pedometers worn by participants, as well as from questionnaires before and after the intervention. Blood pressure, weight, and cholesterol are measured before and after the intervention.

  Eligibility

Ages Eligible for Study:   60 Years and older
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Age greater than 60 years
  • Female
  • African American

Exclusion Criteria:

  • Use of walker for ambulation
  • Positive response on a modified Physical Activity Readiness Questionnaire, indicating potential risk of engaging in activity
  • Withdrawal by primary physician
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00473044

Locations
United States, California
University of California, Los Angeles
Los Angeles, California, United States, 90095
Sponsors and Collaborators
Investigators
Principal Investigator: Obidiugwu Kenrik Duru, MD David Geffen School of Medicine, University of California, Los Angeles
  More Information

Publications:
Responsible Party: Obidiugwu Kenrik Duru, MD, MS, University of California, Los Angeles
ClinicalTrials.gov Identifier: NCT00473044     History of Changes
Other Study ID Numbers: AG0085, R01 AG024460
Study First Received: May 10, 2007
Last Updated: December 29, 2008
Health Authority: United States: Federal Government

ClinicalTrials.gov processed this record on April 22, 2014