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OpenTrials
Completed

NCT Number: NCT00473044

An Intervention to Increase Physical Activity Among African American Women

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.

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Key information

Age range

60 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University of California, Los Angeles

Los Angeles, California, 90095, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Sisters in Motion

Behavioral

Primary outcomes

  1. Change in weekly steps walked as measured by pedometer

    Time frame: 10 weeks and 6 months

Secondary outcomes

  1. Change in weekly metabolic equivalents expended in physical activity

    Time frame: 10 weeks and 6 months

  2. Change in blood pressure, weight, and low-density lipoprotein (LDL) cholesterol

    Time frame: 10 weeks and 6 months

Sponsors and collaborators

Lead sponsor

National Institute on Aging (NIA)

Nih

Registry information

Important dates

Study start
2006
Primary completion
2008
Study completion
2008
First posted
May 14, 2007
Registry last updated
Dec 31, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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