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

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.

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