Empowering Mindfulness, Body Respect, and Compassionate Eating Among Women Who Binge Eat During Pregnancy

EMBRACE MOMS 2 BE: A Pilot Feasibility, Acceptability, and Preliminary Efficacy Study of a Mindful Eating Self-Help Program for Women Who Binge Eat During Pregnancy

Primary Study Aims:

1. To evaluate the feasibility, acceptability, and preliminary efficacy of a 10-week mindful eating self-help program for women who binge eat during pregnancy. Primary efficacy targets will include measures of mindful eating and binge eating. Secondary efficacy targets will involve measures of body image and well-being.
2. To evaluate the incremental utility of adding use of a companion mindful eating smart phone application for enhancing the acceptability and preliminary efficacy of the program.
3. To gain insights into ways in which this program may be better tailored to the experiences of pregnancy for future program adaptation and refinement.

Study Overview

• Status: Withdrawn
• Conditions: Pregnancy; Binge Eating
• Intervention / Treatment: Behavioral: Mindful Eating Self-Help Program; Behavioral: Mindful Eating Smartphone Application (Am I Hungry? Virtual Coach)

Detailed Description

Research suggests that binge eating during pregnancy may adversely impact maternal-child health and well-being. For example, clinical evidence cites binge eating as a risk factor for increased gestational weight gain, cesarean delivery, giving birth to infants who are large for gestational age (LGA), and is associated with additional maternal susceptibility for cardiometabolic dysregulation and its complications at this critical maturational period . Nevertheless, surprisingly despite the growth in epidemiological investigations of eating disorders during pregnancy, no studies to date have specifically evaluated a behavioral intervention during pregnancy to address binge eating concerns within this population. Therefore, there is significant need to address this gap in order to develop, evaluate, and disseminate evidence-based behavioral interventions for women struggling with binge eating during pregnancy. One growing area of scholarship is implementing self-help approaches as a means of increasing availability to evidence-based behavioral health interventions for individuals who may not otherwise be able to access these treatments. At the same time, interventions that incorporate mindful eating have recently shown promise as an effective intervention for reducing binge eating and overeating in a wide range of clinical and community samples. These interventions most often conducted over a period ranging between 6-20 weeks of varying formats (e.g., group, in-person versus combination with remote support, etc.), and intensities (e.g., weekly versus bi-weekly, etc.), typically introduce participants to the concepts of mindfulness, provide opportunities to engage in mindfulness meditation practices, apply mindfulness skills to the process of eating via eating-related meditations and other similar exercises including appetite awareness training and encourage between-session home practice. The Am I Hungry? Mindful Eating Program for Binge Eating was used as a model for the present study. In the original pilot investigation a sample of women with binge eating disorder engaged in a 10-week group mindful eating-based treatment program. Results indicated significant reductions in binge eating severity and psychological distress by the final assessment period which were sustained at 1-year follow-up. We have adapted this approach in order to evaluate it in a guided self-help format with and without access to a companion smartphone application and among other things to directly assess not only changes in binge eating but also those related to more adaptive eating processes such as mindful and intuitive eating styles.

• Study Type: Interventional
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • North Carolina
    • Charlotte, North Carolina, United States, 28223
      • UNC Charlotte

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 40 years (Adult)
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

• female (assigned sex at birth)
• able to read and write in English
• between the ages of 18-40
• lives in the United States
• between 13-16 weeks pregnant (gestation) with a singleton
• owns an iPhone or iPad
• reports engaging in recurrent binge eating (i.e., reporting engaging in at least 1 binge eating episode per week for the last 28 days according to the EDE-Qi)
• has access to a computer or tablet with Internet
• being regularly followed by a healthcare provider during their pregnancy

Exclusion Criteria:

• reports current smoking or substance abuse
• reports elevated depression (i.e., a score of 13 or higher on the EPDS)
• reports current suicidal ideation (assessed on the EPDS)
• reports anorexia, purging or compensatory behavior (both assessed on the EDE-Qi)
• reports a history of being hospitalized for mental health treatment in the last 6 months
• reports use of medications that are taken to affect appetite or metabolism (e.g., insulin)
• is currently in therapy for treating binge eating
• reports serious cardiovascular morbidity (e.g., hypertension)
• reports uncontrolled or untreated thyroid disease
• reports a history of 3 or more miscarriages, weakened cervix, or persistent bleeding during the first 12 weeks of pregnancy
• reports being unable to commit to participate fully in the 10-week program (i.e., read from the self-help book weekly, utilize the smartphone application daily, submit weekly logs of their experiences)
• individuals seeking a dieting approach to weight management during pregnancy

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Double

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: Mindful Eating Self-Help Book Only; Participants will be invited to read about and practice a variety of mindful eating-related strategies over the course of 10 weeks based on Dr. Michelle May & Dr. Kari Anderson's self-help book entitled, "Eat What You Love, Love What You Eat for Binge Eating". Participants will also be asked to complete a weekly electronic log describing their experiences with the weekly mindfulness-based practices.	Behavioral: Mindful Eating Self-Help Program; 10-week exposure to mindful eating principles and practices outlined in the Eat What You Love, Love What You Eat for Binge Eating book
Experimental: Mindful Eating Self-Help Book + Smartphone App; Participants will be invited to read about and practice a variety of mindful eating-related strategies over the course of 10 weeks based on Dr. Michelle May & Dr. Kari Anderson's self-help book entitled, "Eat What You Love, Love What You Eat for Binge Eating". In addition, participants will be asked to use the companion Am I Hungry? Mindful Eating Virtual Coach smartphone application three times daily. Participants will also be asked to complete a weekly electronic log describing their experiences with the weekly mindfulness-based practices.	Behavioral: Mindful Eating Self-Help Program; 10-week exposure to mindful eating principles and practices outlined in the Eat What You Love, Love What You Eat for Binge Eating book; Behavioral: Mindful Eating Smartphone Application (Am I Hungry? Virtual Coach); 10-week exposure to using a mindful eating mobile phone application daily.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Mindful Eating	Mindful Eating Inventory (MEI)	baseline, after week 5 (midpoint), after week 10 (immediate post)
Binge Eating	Eating Disorders Examination-Questionnaire with Instructions (EDE-Qi)	baseline, after week 5 (midpoint), after week 10 (immediate post)
Intuitive Eating	Intuitive Eating Scale-2 (IES-2)	baseline, after week 5 (midpoint), after week 10 (immediate post)
Enrollment	percent enrollment within 6 months of opening recruitment	6 months after opening enrollment
Attrition	percent of participants who dropped out	throughout the 10-week program
Program Satisfaction	participant satisfaction questionnaire	after week 10
App Usability	app usability questionnaire	after week 10

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Body Image	Body Image in Pregnancy Scale (BIPS)	baseline, after week 5 (midpoint), after week 10 (post-program)
General Well-being	General Well-being: Warwick-Edinburgh Mental Well-being Scale (WEMWBS)	baseline, after week 5 (midpoint), after week 10 (post-program)
COVID-19-related Well-being	Perinatal COVID-19-related Well-being (COPE-IU)	baseline, after week 5 (midpoint), after week 10 (post-program)
Mindful Self-Care	Mindful Self-Care Scale (MSCS)	baseline, after week 5 (midpoint), after week 10 (immediate post)
Weight Bias Internalization	Weight Bias Internalization Scale-Modified (WBIS-M)	baseline, after week 5 (midpoint), after week 10 (immediate post)
Physical Activity	International Physical Activity Questionnaire-Short Form (IPAQ-SF)	baseline, after week 5 (midpoint), after week 10 (immediate post)
Depression	Edinburgh Postnatal Depression Scale (EPDS)	baseline, after week 5 (midpoint), after week 10 (immediate post)

Collaborators and Investigators

• Sponsor: University of North Carolina, Charlotte
• Investigators: Principal Investigator: Jennifer B Webb, PhD, UNC Charlotte; Principal Investigator: V Gil-Rivas, PhD, UNC Charlotte

Study record dates

Study Major Dates

• Study Start (Actual): February 11, 2024
• Primary Completion (Actual): March 10, 2024
• Study Completion (Actual): March 10, 2024

Study Registration Dates

• First Submitted: July 16, 2022
• First Submitted That Met QC Criteria: October 11, 2022
• First Posted (Actual): October 14, 2022

Study Record Updates

• Last Update Posted (Actual): May 7, 2026
• Last Update Submitted That Met QC Criteria: May 3, 2026
• Last Verified: May 1, 2026

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Hyperphagia; Signs and Symptoms, Digestive; Pathological Conditions, Signs and Symptoms; Signs and Symptoms; Bulimia
• Other Study ID Numbers: IRBIS-19-0680

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No