Actively Recruiting
Expectant Moms Managing Attention-Deficit/ Hyperactivity Disorder
Led by University of Pittsburgh · Updated on 2026-05-07
80
Participants Needed
1
Research Sites
109 weeks
Total Duration
On this page
Sponsors
U
University of Pittsburgh
Lead Sponsor
U
University of Maryland, College Park
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this study is to test a behavioral program for pregnant individuals with ADHD. This behavioral program focuses on skills for managing ADHD and related symptoms in pregnancy and postpartum. This pilot effectiveness-implementation trial aims to (1) preliminarily evaluate the MomMA behavioral intervention compared to treatment as usual (TAU) on clinical outcomes and (2) evaluate implementation outcomes, including feasibility and acceptability of clinic screening within existing OB workflows; assessment and intervention protocols; provider training/fidelity to manual; and all other study protocols from the perspective of real-world providers and participants.
CONDITIONS
Official Title
Expectant Moms Managing Attention-Deficit/ Hyperactivity Disorder
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Meets full DSM-5 criteria for ADHD
- Is between 14 and 22 weeks of gestation
- Is 18 years of age or older
- English speaking
- Lives in Pennsylvania
You will not qualify if you...
- Substance use disorders requiring dual diagnosis treatment
- Intellectual disability
- Bipolar disorder, psychosis, or major depressive disorder with suicidal ideation
- High complexity medical conditions during pregnancy, including maternal cancer, multiples, placenta accreta, or fetus known to have a severe congenital condition
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
UPMC Magee-Womens Hospital
Pittsburgh, Pennsylvania, United States, 15213
Actively Recruiting
Research Team
M
Michelle Wilson, Research Coordinator
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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