- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02416921
Preventing Weight Gain in African American Reproductive-Aged Women (FB--Pilot)
May 20, 2016 updated by: Washington University School of Medicine
Preventing Weight Gain in African American Reproductive-Aged Women: Pilot Program
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed 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.
Study Type
Interventional
Enrollment (Actual)
18
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Missouri
-
Saint Louis, Missouri, United States, 63110
- Washington University School of Medicine
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 35 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Weight-gain Prevention
Subjects in this group will engage in a 4-week weight-gain prevention curriculum delivered via Facebook
|
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.
|
Active Comparator: Women's Health
Subjects in this group will engage in a 4-week women's health curriculum delivered via Facebook
|
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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Program satisfaction, as measured by the OWN Program Satisfaction Survey
Time Frame: 9 weeks, beginning with start of cohort
|
9 weeks, beginning with start of cohort
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Rick Stein, PhD, Washington University School of Medicine
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
April 1, 2015
Primary Completion (Actual)
September 1, 2015
Study Completion (Actual)
September 1, 2015
Study Registration Dates
First Submitted
March 18, 2015
First Submitted That Met QC Criteria
April 14, 2015
First Posted (Estimate)
April 15, 2015
Study Record Updates
Last Update Posted (Estimate)
May 23, 2016
Last Update Submitted That Met QC Criteria
May 20, 2016
Last Verified
May 1, 2016
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 201412141
- 1P30DK092950 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Obesity
-
Central Hospital, Nancy, FranceNot yet recruiting
-
University of MinnesotaNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)Active, not recruitingAdolescent ObesityUnited States
-
Helsinki University Central HospitalKarolinska Institutet; Folkhälsan Researech CenterEnrolling by invitation
-
Istanbul Medipol University HospitalMedipol UniversityCompletedObesity, Morbid | Obesity, Adolescent | Obesity, Abdominal | Weight, Body | Obesity, VisceralTurkey
-
Queen Fabiola Children's University HospitalNot yet recruitingMorbid Obesity | Adolescent Obesity | Bariatric SurgeryBelgium
-
Washington University School of MedicinePatient-Centered Outcomes Research Institute; Pennington Biomedical Research... and other collaboratorsActive, not recruitingOvernutrition | Nutrition Disorders | Overweight | Body Weight | Pediatric Obesity | Body Weight Changes | Childhood Obesity | Weight Gain | Adolescent Obesity | Obesity, Childhood | Overweight and Obesity | Overweight or Obesity | Overweight AdolescentsUnited States
-
Azienda Ospedaliero-Universitaria Consorziale Policlinico...Institute of Biomembranes, Bioenergetics and Molecular Biotechnologies; Istituti... and other collaboratorsCompletedMorbid Obesity | Metabolically Healthy ObesityItaly
-
The Hospital for Sick ChildrenCompleted
-
Ihuoma EneliCompletedObesity, ChildhoodUnited States
-
Fundació Sant Joan de DéuRecruitingObesity, Childhood | Obesity, AdolescentSpain
Clinical Trials on Weight-gain Prevention
-
Pennington Biomedical Research CenterEunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaboratorsCompleted
-
University of MinnesotaHealthy Foods Healthy LivesCompletedObesityUnited States
-
University of MinnesotaNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)Completed
-
M.D. Anderson Cancer CenterLance Armstrong FoundationUnknown
-
National Institute of Diabetes and Digestive and...Completed
-
Norwegian School of Sport SciencesCompletedPregnancy | Excessive Weight GainNorway
-
The Miriam HospitalNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)Unknown
-
University of Colorado, DenverUnited States Department of Agriculture (USDA)Completed
-
University of TennesseeMayo Clinic; National Institute of Diabetes and Digestive and Kidney Diseases...CompletedSmoking Cessation | Weight Change, BodyUnited States
-
Consumer Wellness SolutionsNorthwestern University; SRI InternationalCompletedObesity | Overweight | Cigarette SmokingUnited States