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OpenTrials
Completed

NCT Number: NCT02416921

Preventing Weight Gain in African American Reproductive-Aged Women

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.

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Key information

Age range

18 year–35 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Washington University School of Medicine

St Louis, Missouri, 63110, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

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

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

Treatment and study plan

Weight-gain Prevention

Behavioral

A 4-week weight-gain prevention curriculum will be delivered via Facebook. Participants will be provided tips to prevent weight-gain and will be given the opportunity to engage with the peer coaches and other participants in the group.

Women's Health

Behavioral

A 4-week women's health curriculum will be delivered via Facebook. Participants will be provided tips for staying healthy and will be given the opportunity to engage with the peer coaches and other participants in the group.

Primary outcomes

  1. Program satisfaction, as measured by the OWN Program Satisfaction Survey

    Time frame: 9 weeks, beginning with start of cohort

Sponsors and collaborators

Lead sponsor

Washington University School of Medicine

Other

Collaborators

  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
  • University of Massachusetts, Worcester
  • University of Missouri, Kansas City

Registry information

Official study title

Preventing Weight Gain in African American Reproductive-Aged Women: Pilot Program

Acronym: FB--Pilot

Important dates

Study start
2015
Primary completion
2015
Study completion
2015
First posted
Apr 15, 2015
Registry last updated
May 23, 2016

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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