Preventing Weight Gain in African American Reproductive-Aged Women (FB--Pilot)

The Washington University

Status: Completed

Conditions: Women's Health; Weight Gain; Obesity

Treatments: Behavioral: Weight-gain Prevention; Behavioral: Women's Health

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT02416921

1P30DK092950 (U.S. NIH Grant/Contract)

201412141

Details and patient eligibility

About

The purpose of this research study is to evaluate the effect of a Facebook-delivered weight-gain prevention program versus a Facebook-delivered program with general women's health information.

Full description

Weight gain is an important health concern, and disparities in the prevalence of obesity between African American and White women increase throughout the reproductive period. This study is a randomized, controlled trial testing the feasibility and acceptability of a peer-coach-administered, Facebook-delivered intervention to prevent weight gain in overweight and obese African American women. Study visits lasting approximately 1 hour will occur at baseline, post-intervention, and 1-month follow-up, to assess effectiveness and acceptability. The core intervention will occur over a 4-week period. Educational content in both the weight-gain prevention program and women's health program will be delivered via Facebook, with new content posted each weekday related to that week's topics. The peer coaches may contact participants via private messaging, when needed, to provide support and encourage engagement. If successful, this intervention could be easily disseminated to populations in under-served and community settings.

Enrollment: 18 patients

Sex: Female

Ages: 18 to 35 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• African American
• Has Facebook account and uses it, on average, at least once a day
• Body Mass Index (BMI) of 25-45
• Has access to the internet
• Able to consent in English

Exclusion criteria

• Currently pregnant or breastfeeding, recently postpartum (within 6 weeks)
• Diagnosis of Diabetes Mellitus
• History of contraindicated medical conditions or conditions that can affect weight
• Current use of certain medications

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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18 participants in 2 patient groups

Weight-gain Prevention

Experimental group

Description:

Subjects in this group will engage in a 4-week weight-gain prevention curriculum delivered via Facebook

Treatment:

Behavioral: Weight-gain Prevention

Women's Health

Active Comparator group

Description:

Subjects in this group will engage in a 4-week women's health curriculum delivered via Facebook

Treatment:

Behavioral: Women's Health