MedPath

Facebook to Promote Physical Activity in Black Women African American Women

Not Applicable
Completed
Conditions
Physical Activity
Registration Number
NCT02372565
Lead Sponsor
Arizona State University
Brief Summary

The purpose of this study is to evaluate the feasibility of a social media and text-message-delivered, Social Cognitive Theory-based, culturally relevant intervention designed to promote physical activity among African American women. An 8-week, 2-arm randomized trial will be implemented. Arm 1 will receive a culturally-relevant, technology-based physical activity intervention delivered via Facebook and text messages. Arm 2 (Comparison Group) will receive a standard print-based physical activity promotion materials consisting of high quality physical activity promotion brochures produced by the American Heart Association.

Detailed Description

The purpose of this study is to apply and investigate the feasibility of a social media and text-message-delivered, Social Cognitive Theory-based, culturally relevant intervention designed to promote physical activity among African American women. In an 8-week, 2-arm randomized trial, 30 African American women will be assigned to receive either: a) culturally-relevant, technology-based physical activity intervention delivered via Facebook and text messages, or b) a standard print-based physical activity promotion intervention consisting of high quality physical activity promotion brochures produced by the American Heart Association delivered via USPS mail.

Aim 1: Test the feasibility of a culturally relevant, social media and text-message delivered physical promotion pilot intervention among adult African American women. The investigators hypothesize that the culturally relevant Facebook and text message delivered intervention will be feasible as measured by the acceptability, implementation, and practicality of the intervention program.

Aim 2: Examine the impact of the culturally-relevant, Facebook and text message delivered intervention to increase physical activity and enhance associated Social Cognitive Theory constructs explicitly targeted by the intervention activities. Physical activity will be objectively measured by accelerometers and Social Cognitive Theory constructs of self-efficacy, social support, self-regulation, and outcome expectations will be assessed by validated self-report questionnaires. The investigators hypothesize that participants receiving the culturally-adapted, Social Cognitive Theory-based Facebook and text-message intervention will demonstrate higher physical activity levels and greater enhancements in Social Cognitive Theory constructs when compared to the standard print-based intervention group at the post-intervention assessment.

Aim 3: Examine the preliminary effect of a culturally relevant, social media-delivered physical activity promotion intervention on anthropometric, blood pressure, and blood lipid outcomes. The investigators hypothesize that increased physical activity at the post-intervention follow-up will be associated with improvements in these variables.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
30
Inclusion Criteria
  • self-identified as African American
  • female
  • insufficiently active (<150 min/week of moderate-intensity physical activity assessed by the short version of the International Physical Activity Questionnaire)
  • aged 24-49 years
  • having an active Facebook account
  • ability to read/write in English
Exclusion Criteria
  • concurrent participation in another physical activity promotion program (research or commercial)
  • being pregnant or planning on becoming pregnant in the next 6 months, and
  • self-reported condition that inhibits engagement in physical activity
  • contraindication for physical activity according to the Physical Activity Readiness Questionnaire (PAR-Q) unless written permission from the participant's physician to engage in the study is provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Feasibility of Using Facebook and Text Messaging to Deliver a Physical Activity Program to African American WomenPost Intervention (up to 8 weeks)

Measured using a composite score by assessing acceptability (participants perceived satisfaction and usefulness of the program; perceived cultural relevance of the program), demand (interest in study participation; participant retention), and implementation (participant activity on the Facebook group page, successful delivery of text messages, successful delivery of study materials on the study Facebook wall) of the culturally relevant physical activity program.

Secondary Outcome Measures
NameTimeMethod
Change in self-regulation for physical activity from baseline to 8 weeksTwo assessments, 8 weeks apart

Assessed by the Self-Regulation Scale from the Health Beliefs Survey (Anderson, 2010)

Change in serum high-density lipoprotein (HDL) cholesterol from baseline to 8 weeksTwo assessments, 8 weeks apart
Change in serum triglycerides from baseline to 8 weeksTwo assessments, 8 weeks apart
Change in total serum cholesterol from baseline to 8 weeksTwo assessments, 8 weeks apart
Change in serum low-density lipoprotein (LDL) cholesterol from baseline to 8 weeksTwo assessments, 8 weeks apart
Change in physical activity from baseline to 8 weeksTwo assessments, 8 weeks apart

Assessed by ActiGraph GT3X+ accelerometers

Change in exercise self-efficacy from baseline to 8 weeksTwo assessments, 8 weeks apart

Assessed by the Exercise Confidence Survey (Sallis, 1988)

Change in social support for exercise from baseline to 8 weeksTwo assessments, 8 weeks apart

Assessed by the Social Support for Exercise Survey (Sallis,1987)

Change in outcome expectations for exercise from baseline to 8 weeksTwo assessments, 8 weeks apart

Assessed by the Outcome Expectation Scale for Exercise (Resnick, 2000)

Change in body mass index (BMI) from baseline to 8 weeksTwo assessments, 8 weeks apart

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.