Body Acceptance After Baby Intervention (BABI)

February 12, 2026 updated by: Northeastern University
The purpose of this study is to learn if a novel online single-session intervention can help improve body dissatisfaction in new moms. The active intervention condition, Body Acceptance After Baby (BABI), uses acceptance-based skills to help participants cope with body dissatisfaction. BABI will be evaluated against another active intervention condition (a brief infographic that provides psychoeducation about body image during postpartum) and a waitlist control condition.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

375

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 Contact

Study Locations

    • Massachusetts
      • Boston, Massachusetts, United States, 02115

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Individuals must:

  • Be currently residing in the U.S.
  • Be able to read and write in English
  • Be aged 18 or above
  • Identify as a woman
  • Have given birth to a live infant in the past year
  • Endorse dissatisfaction with their appearance (i.e., in answering the question "Indicate how satisfied you are with your overall appearance" they must answer neutral, mostly dissatisfied, or very dissatisfied)

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Body Acceptance After Baby Intervention (BABI)
The active condition, BABI, includes (1) psychoeducation about body image during postpartum; (2) psychoeducation about acceptance; (3) an activity to practice "unhooking" (cognitive defusion skill); (4) a values clarification exercise; (5) a peer advice activity (participants give advice in response to vignettes of new moms who are struggling with body image); and (6) the creation of a personalized action plan. BABI is designed to take approximately 30 minutes.
BABI is an online, self-directed single-session intervention designed to improve body dissatisfaction in postpartum moms (up to one year after delivery) aged 18 or older.
Experimental: Postpartum Body Image Infographic
Participants will read a brief infographic that includes (1) psychoeducation about body image and the harms of "bounce-back" culture during postpartum and (2) ways to improve body image. This infographic is designed to be read in approximately 2 minutes.
The postpartum body image infographic is an online pamphlet that provides psychoeducation about body image during postpartum.
No Intervention: Waitlist Control
This group will receive no intervention, but will be given access to both active conditions at the end of follow-ups.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Postpartum body image
Time Frame: Baseline, 1 month, 3 months
Postpartum body image will be measured using the Body Image in Pregnancy Scale adapted for postpartum. Only the following subscales will be measured: (1) Preoccuptation with Physical Appearance; (2) Prioritization of Appearance over Function; (3) Appearance-Related Behavioral Avoidance. Subscales range from 1-5 with higher scores indicating greater body image disturbance.
Baseline, 1 month, 3 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Body appreciation
Time Frame: Baseline, 1 month, 3 months
Body Appreciation will be measured using The Body Appreciation Scale-2 Short Form. Scores range from 3-15 with higher scores indicating greater body appreciation.
Baseline, 1 month, 3 months
Psychological flexibility
Time Frame: Baseline, 1 month, 3 months
Psychological flexibility will be measured with the Comprehensive assessment of Acceptance and Commitment Therapy processes (CompACT). Scores range from 0-138 with higher scores indicating greater psychological flexibility. Subscales can also be calculated to measure (1) Openness to Experience, (2) Behavioral Awareness, and (3) Valued Action.
Baseline, 1 month, 3 months
Postpartum depression
Time Frame: Baseline, 1 month, 3 months
Postpartum depression will be measured with the Edinburgh Postnatal Depression Scale (EPDS). Scores range from 0-30 with higher scores indicating greater depressive symptoms.
Baseline, 1 month, 3 months
Eating disorder symptoms
Time Frame: Baseline, 1 month, 3 months
Eating disorder symptoms will be measured with the Eating Disorder Examination Questionnaire Short (EDE-QS). Scores range from 0-36 with higher scores indicating greater severity of eating disorder symptoms.
Baseline, 1 month, 3 months
Intuitive eating
Time Frame: Baseline, 1 month, 3 months
Intuitive eating will be measured with the Intuitive Eating Scale-3 (IES-3) . Each item ranges from 1-5 and can be averaged to obtain a global score with higher scores indicating greater intuitive eating. Subscale scores (Unconditional Permission to Eat; Eating for Physical Reasons; Reliance on Hunger and Satiety Cues; Body-Food Choice Congruence) can also be calculated.
Baseline, 1 month, 3 months
Breastfeeding self-efficacy
Time Frame: Baseline, 1 month, 3 months
Breastfeeding self-efficacy will be measured with the Breastfeeding Self-Efficacy Scale (BSES-SF). Scores range from 14-70 with higher scores indicating greater self-efficacy.
Baseline, 1 month, 3 months
Bottle-feeding self-efficacy
Time Frame: Baseline, 1 month, 3 months
Bottle-feeding self-efficacy will be measured with the Bottle Feeding Self-Efficacy Scale. Scores range from 20-100 with higher scores indicating greater self-efficacy.
Baseline, 1 month, 3 months
State mood and body image
Time Frame: Baseline
Visual analog scales will be used to measure state anxiety, negative affect, positive affect, appearance satisfaction, weight satisfaction, muscle tone satisfaction, confidence, body acceptance, body positivity, anger, body functionality appreciation, body appreciation, broad concept of beauty (body sizes and body shapes) and body positive protective filter. Each item ranges from 0-100 with greater scores indicating greater levels of the respective variable.
Baseline
Hopelessness
Time Frame: Baseline
Hopelessness will be measured with the Beck Hopelessness Scale - 4-item version (BHS). Each item ranges from 0-3. Items are averaged to obtain a total score with higher scores indicating greater hopelessness.
Baseline

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Acceptability
Time Frame: Baseline
To measure intervention acceptability we will use the The Program Feedback Scale (PFS). The PFS asks participants to rate agreement with seven statements about the acceptability of the SSI (e.g. "I enjoyed the program") on a five-point scale. Higher scores reflect greater acceptability for each item.
Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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 (Actual)

January 20, 2026

Primary Completion (Estimated)

December 1, 2027

Study Completion (Estimated)

December 1, 2027

Study Registration Dates

First Submitted

November 14, 2025

First Submitted That Met QC Criteria

February 12, 2026

First Posted (Actual)

February 20, 2026

Study Record Updates

Last Update Posted (Actual)

February 20, 2026

Last Update Submitted That Met QC Criteria

February 12, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

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

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.

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