Change Clubs for African American Women

Preliminary Investigation of Civic Engagement as a Novel Approach to Behavior Change and Body Weight Improvement in African American Females

African American women have among the highest rates of overweight and obesity and few meet dietary or physical activity guidelines. The investigators seek to develop a new intervention strategy that will help alleviate health disparities, thereby improving quality of life, health care costs, and disease burden. The African American Collaborative Obesity Research Network (AACORN) recommends an eco-social, community-engaged approach to behavior change that is in line with cultural values of interconnectedness and care for others. The purpose of this study is to operationalize the AACORN paradigm to promote improvements in weight status and health through a civic engagement approach. To achieve this, participants will meet in church-based Change Clubs and be led through a 6 month curriculum, which includes both lessons in cardiovascular risk reduction and a civic engagement project. Civic engagement may lead to change in individual health behaviors by increasing self-regulation and self-efficacy. The investigators will measure club members' adherence to the Change Club intervention, defined as average number of sessions attended, retention in the clubs, satisfaction with the Change Club experience and achievement of at least 50% of self-identified benchmarks for community change within 6 months. In addition the investigators will compare anthropometric factors, diet and physical activity behaviors, blood pressure, cardiorespiratory fitness, and psychosocial factors before and after participation in the Change Club intervention.

Study Overview

• Status: Completed
• Conditions: Obesity; Cardiovascular Disease
• Intervention / Treatment: Behavioral: Change Club Intervention

• Study Type: Interventional
• Enrollment (Actual): 26
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • Massachusetts
    • Boston, Massachusetts, United States, 02111
      • Friedman School of Nutrition, Tufts University

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 30 years to 70 years (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: Female

Description

Inclusion Criteria:

• female;
• age 30-70 years;
• self-identified as African American;
• English-speaking;
• BMI ≥25.0;
• currently sedentary (not meeting Physical Activity Guidelines for Americans);
• safe to initiate moderate physical activity per the PAR-Q.

Exclusion Criteria:

• failure to provide informed consent;
• participation in any other lifestyle modification program;
• current use of either prescription or over-the-counter weight loss medications;
• inability to communicate due to severe,
• uncorrectable hearing loss or speech disorder;
• severe visual impairment (if it precludes completion of assessments and/or intervention);
• planning to move outside of area within 6 months;
• pregnancy (since weight loss, the primary outcome, is inadvisable in this population).

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Prevention
• Allocation: N/A
• Interventional Model: Single Group Assignment

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Change Club Intervention	Behavioral: Change Club Intervention

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in Weight from Pre to Post-Intervention (6 Months)	Body weight will be measured in triplicate to the nearest 0.5 kg using a digital floor scale (Seca 876).	pre-post; participants will be followed for the 6-month intervention period

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in Diet from Pre to Post-Intervention (6 Months)	Two 24-hour recalls (1 weekday and 1 weekend day) will be collected. Data will be entered into the Nutrition Data System for Research (NDSR). Nutrient and food group calculations will be performed using the NDSR software.	pre-post; participants will be followed for the 6-month intervention period
Change in Physical Activity Level from Pre to Post-Intervention (6 Months)	Physical activity levels will be measured objectively using accelerometers (ActiGraph GT3X worn for 7 days) and by self-report (7-Day Physical Activity Recall).	pre-post; participants will be followed for the 6-month intervention period
Change in Blood Pressure from Pre to Post-Intervention (6 Months)	Blood pressure will be measured to the nearest 1mm Hg using a validated automated monitor (Omron HEM-705CP), using American Heart Association guidelines.	pre-post; participants will be followed for the 6-month intervention period
Change in Cardiorespiratory Fitness Level from Pre to Post-Intervention (6 Months)	Cardiovascular fitness will be measured using the Rockport 1-mile walk test. Participants will walk a flat, 1-mile course as fast as possible without running. Heart rate will be measured immediately after. VO2max will be estimated from validated formulas using 1-mile walk time, gender, age, body weight, and ending heart rate.	pre-post; participants will be followed for the 6-month intervention period
Change in Self-Efficacy from Pre to Post-Intervention (6 Months)	Self-efficacy will be assessed the Weight Efficacy Life-Style Questionnaire (Clark 1991). The exercise self-efficacy scale contains 5 items measuring confidence in ability to exercise under various challenges.	pre-post; participants will be followed for the 6-month intervention period
Change in Collective Efficacy from Pre to Post-Intervention (6 Months)	Collective efficacy will be measured using an adapted 8-item Likert style scale (Sampson, Raudebush, & Earls 1997) that examines the extent to which individuals in a neighborhood or community trust and help others.	pre-post; participants will be followed for the 6-month intervention period
Change in Percent Body Fat from Pre to Post-Intervention (6 Months)	Percent body fat will be measured by bioelectric impedance using a Tanita TBF-410 Bioelectric Impedance Body Composition Analyzer.	pre-post; participants will be followed for the 6-month intervention period
Change in Perceived Stress from Pre to Post-Intervention (6 Months)	Perceived stress will be measured using the validated 14-item Perceived Stress Scale (Cohen 1983).	pre-post; participants will be followed for the 6-month intervention period
Change in Level of Civic Engagement from Pre to Post-Intervention (6 Months)	We will use the Civic Engagement Scale (Doolittle and Faul 2013) to assess civic engagement.	pre-post; participants will be followed for the 6-month intervention period
Change in Level of Self-Regulation from Pre to Post-Intervention (6 Months)	Self-regulation will be measured using a scale developed by Saelens et al. (2000) to measure self-regulatory skill usage for exercise and for controlled eating.	pre-post; participants will be followed for the 6-month intervention period

Other Outcome Measures

Outcome Measure	Time Frame
Adherence	attendance will be monitored throughout the 6-month intervention period
Retention	participant retention will be monitored throughout the 6-month intervention period

Collaborators and Investigators

• Sponsor: Tufts University
• Collaborators: Boston Nutrition Obesity Research Center (administered by Boston Medical Center)

Publications and helpful links

General Publications

• Brown AG, Hudson LB, Chui K, Metayer N, Lebron-Torres N, Seguin RA, Folta SC. Improving heart health among Black/African American women using civic engagement: a pilot study. BMC Public Health. 2017 Jan 24;17(1):112. doi: 10.1186/s12889-016-3964-2.

Study record dates

Study Major Dates

• Study Start: December 1, 2013
• Primary Completion (Actual): November 1, 2015
• Study Completion (Actual): February 1, 2017

Study Registration Dates

• First Submitted: June 10, 2014
• First Submitted That Met QC Criteria: June 24, 2014
• First Posted (Estimate): June 25, 2014

Study Record Updates

• Last Update Posted (Actual): September 5, 2017
• Last Update Submitted That Met QC Criteria: September 1, 2017
• Last Verified: September 1, 2017

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Cardiovascular Diseases
• Other Study ID Numbers: 11244 (Other Grant/Funding Number: PCORI)