An Intervention to Increase Physical Activity Among African American Women

NCT ID: NCT00473044

Last Updated: 2008-12-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

104 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-04-30

Study Completion Date

2008-01-31

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Sedentary Lifestyle Inactivity

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Interventions

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Sisters in Motion

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

60 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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National Institute on Aging (NIA)

NIH

Sponsor Role lead

Responsible Party

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University of California, Los Angeles

Principal Investigators

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Obidiugwu Kenrik Duru, MD

Role: PRINCIPAL_INVESTIGATOR

David Geffen School of Medicine, University of California, Los Angeles

Locations

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University of California, Los Angeles

Los Angeles, California, United States

Site Status

Countries

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United States

References

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Dunn AL, Blair SN. Translating evidenced-based physical activity interventions into practice. The 2010 challenge. Am J Prev Med. 2002 May;22(4 Suppl):8-9. doi: 10.1016/s0749-3797(02)00432-4. No abstract available.

Reference Type BACKGROUND
PMID: 11985931 (View on PubMed)

American College of Sports Medicine. Physical activity programs and behavior counseling in older adult populations. Med Sci Sports Exerc. 2004 Nov;36(11):1997-2003. doi: 10.1249/01.mss.0000145451.08166.97.

Reference Type BACKGROUND
PMID: 15514518 (View on PubMed)

Brawley LR, Rejeski WJ, King AC. Promoting physical activity for older adults: the challenges for changing behavior. Am J Prev Med. 2003 Oct;25(3 Suppl 2):172-83. doi: 10.1016/s0749-3797(03)00182-x.

Reference Type BACKGROUND
PMID: 14552942 (View on PubMed)

Other Identifiers

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R01AG024460

Identifier Type: NIH

Identifier Source: secondary_id

View Link

AG0085

Identifier Type: -

Identifier Source: org_study_id