- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07422571
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
Status
Recruiting
Conditions
Intervention / Treatment
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
- Name: Rachel Rodgers, PhD
- Phone Number: 617 373 2105
- Email: r.rodgers@northeastern.edu
Study Locations
-
-
Massachusetts
-
Boston, Massachusetts, United States, 02115
- Recruiting
- Northeastern University
-
Contact:
- Rachel Rodgers, PhD
- Phone Number: 617-470-9974
- Email: r.rodgers@northeastern.edu
-
-
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.
Sponsor
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
Keywords
Other Study ID Numbers
- 24-11-25
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.
Clinical Trials on Body Dissatisfaction
-
University of PadovaRecruitingBody Image | Body Dissatisfaction | Eating BehaviorsItaly
-
Hospital de Clinicas de Porto AlegreCompletedBody Dissatisfaction | Disordered EatingBrazil
-
Aarhus University HospitalAalborg Psychiatric HospitalNot yet recruitingPsychiatric Disorder | Eating Disorders | Body Dissatisfaction | Eating Disorder Symptom and Body Image DissatisfactionDenmark
-
University of CalgaryCompletedBody-dissatisfactionCanada
-
Susan GambergQueen Elizabeth II Health Sciences Centre FoundationRecruitingBody Image | Body Dissatisfaction | Dietary Restraint | Negative AffectCanada
-
Karolinska InstitutetUppsala University; Linkoeping UniversityRecruitingEating Disorders | Body DissatisfactionSweden
-
School of Health Sciences GenevaCompletedBody DissatisfactionSwitzerland
-
University of Southern DenmarkTrygFonden, Denmark; Region of Southern Denmark; Danske Regioner; Jascha FondenActive, not recruitingRandomized Controlled Trial | Mental Health Issue | Adolescents | Young Adults | Internet-Based Intervention | Well-Being | Body Dissatisfaction | Online InterventionDenmark
-
University of SheffieldPrincess Nourah Bint Abdulrahman UniversityCompletedEating Disorder Symptom and Body Image DissatisfactionSaudi Arabia
Clinical Trials on Body Acceptance after Baby (BABI)
-
Brigham and Women's HospitalUniversity of Colorado, DenverCompletedGestational Diabetes MellitusUnited States
-
Brigham and Women's HospitalCenters for Disease Control and PreventionCompletedGestational Diabetes MellitusUnited States
-
University of Colorado, DenverCompletedCardiovascular Diseases | Diabetes | Preterm Birth | Overweight and Obesity | Preeclampsia | Gestational Diabetes | Small for Gestational Age at Delivery | Gestational HypertensionUnited States
-
Florida State UniversityCompletedWeight Loss | Self Harm | Eating Behavior
-
Virginia Commonwealth UniversitySociety for the Psychological Study of Social IssuesCompleted
-
University of the West of EnglandNIHR Research for Patient Benefit (RfPB)Completed
-
Universidad Complutense de MadridCompleted
-
University of California, San DiegoChristie's Place; APLA Health; Sister Love; By His Stripes Wellness CenterRecruitingHIV Infections | Trauma | Medication Adherence | Substance UseUnited States
-
Palo Alto Veterans Institute for ResearchRecruitingMusculoskeletal Pain | Chronic PainUnited States
-
Yuzuncu Yil UniversityIstanbul University - CerrahpasaCompletedInfantile Colic | Infantile SpasmTurkey (Türkiye)