The Healthy Moms Study: Comparison of a Post-Partum Weight Loss Intervention Delivered Via Facebook or In-Person Groups

Not Applicable

Completed

Conditions: Diet Modification
Weight Loss
Physical Activity

Interventions: Behavioral: Healthy Moms

Registration Number: NCT03700736

Lead Sponsor: University of Connecticut

Brief Summary: The goal of the project is to conduct a feasibility pilot randomized trial comparing delivery of a post-partum weight loss intervention via Facebook versus via in-person group sessions. The project will provide preliminary data needed to finalize the design of a large randomized trial to compare the non-inferiority and cost-effectiveness of the post-partum weight loss intervention delivered via Facebook versus in-person group sessions. If efficacious and cost-effective, the Facebook-delivered intervention leads naturally to strategies for scaling up for widespread impact.

Detailed Description: Post-partum weight retention contributes to obesity for many women, increasing risk for cardiovascular disease and other chronic diseases and complicating future pregnancies. Lifestyle interventions have shown to be modestly efficacious for post-partum weight loss in randomized controlled trials, yet interventions with numerous visits are logistically challenging for many post-partum women. Innovative and efficacious treatment models for post-partum weight loss that fit into the busy lives of new moms are needed, and cost-effectiveness is critical for adoption. Facebook may be an efficient platform for delivering evidence-based weight loss programming to post-partum women. Delivering interventions via Facebook allows us to connect with post-partum women where they are, more fully integrating into their lives and daily routines. Investigators have developed a post-partum weight loss intervention based on the Diabetes Prevention Program, tailored to needs of post-partum women and for delivery via Facebook. Investigators will conduct a feasibility pilot randomized trial comparing delivery of a post-partum weight loss intervention via Facebook to in-person group sessions. Primary outcomes are the feasibility of recruitment, sustained participation, contamination, retention, and feasibility of assessment procedures in both treatment conditions. Weight loss will be described as an exploratory outcome. The project will provide preliminary data needed to finalize the design of a large randomized trial to compare the non-inferiority and cost-effectiveness of the post-partum weight loss intervention delivered via Facebook versus in-person group sessions. Demonstrating cost-effectiveness in addition to efficacy of our Facebook-delivered post-partum weight loss intervention is critical to support widespread implementation.

Recruitment & Eligibility

Status: COMPLETED

Sex: Female

Target Recruitment: 62

Inclusion Criteria

women 18 years or older
8 weeks to 12 months post-partum at enrollment
overweight or obese (BMI ≥ 25 kg/m2) per measured height and weight at the baseline visit
owns a scale
comfortable reading and speaking in English
owns an iPhone or Android smartphone
active Facebook user
medical clearance (e.g., from primary care provider or obstetrician/gynecologist)
willing and able to participate in either treatment condition (Facebook or in-person)
available to attend in-person meetings over the 6-month study period
45 minutes or less to travel to intervention meetings
willing and able to provide informed consent

Exclusion Criteria

UConn employee or student who is key personnel on the study, UConn employee or student who is a spouse, dependent, or relative of any key personnel, or UConn student who key personnel on this study teaches
women who are currently pregnant or plan to conceive during study period
current participation in clinical weight loss program
Type 1 or Type 2 diabetes
medical conditions affecting weight
medications affecting weight
incapable of walking 1/4 of a mile without stopping
pain that prevents engagement in exercise
previous bariatric surgery
planned surgery during study period
plans to move out of the area during the study period
high depressive symptoms or suicidal ideation
positive screen for binge eating disorder
failure to complete the baseline survey
failure to complete the orientation webinar

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Facebook	Healthy Moms	Women will receive the Healthy Moms intervention, a 6-month behavioral weight loss intervention, via a private ("secret") Facebook group. The weight loss intervention is based on the Diabetes Prevention Program (DPP), an evidence-based lifestyle intervention. A study counselor will facilitate discussions about the topics posted in the Facebook group. Each participant will get an individualized calorie and physical activity goal to help them achieve a healthy weight loss of 1-2 pounds per week. Participants will be encouraged to increase physical activity to 150 minutes per week of moderate intensity activity. Participants will also be encouraged to download the MyFitnessPal app to track daily diet.
Traditional	Healthy Moms	Women will receive the Healthy Moms intervention, a 6-month behavioral weight loss intervention, via in-person 90-minute group sessions (weekly in months 1-4, every other week in months 5-6). The weight loss intervention is based on the Diabetes Prevention Program (DPP), an evidence-based lifestyle intervention. Intervention components will be introduced in the format of handouts, group discussions, and lists of existing resources. Each participant will get an individualized calorie and physical activity goal to help them achieve a healthy weight loss of 1-2 pounds per week. Participants will be encouraged to increase physical activity to 150 minutes per week of moderate intensity activity. Participants will also be encouraged to use an app such as MyFitnessPal to track daily diet.

Primary Outcome Measures

Name	Time	Method
Sustained Participation	6 months	We will calculate sustained participation as time to last intervention session attended in the in-person condition and as time to last post, comment, or reaction (based on date of last post or comment reacted to) in the Facebook condition.
Contamination	6 months	Participants in both treatment conditions will report if they have participated in other weight loss programs (online or in-person), and whether they have searched for weight loss support on Facebook or other online social networks.
Degree of Missingness in Study Measures	12 months	Percent of participants missing data on each measure/item included in data collection at 12 months.
Recruitment	Baseline	Recruitment rates will be calculated from the number of patients approached, screened, consented, and randomized.
Retention	12 months	Retention is calculated as the percentage of participants who complete the 12-month follow-up study assessment in each condition.