MedTrace Logo

Expectant Moms Managing Attention-Deficit/ Hyperactivity Disorder

NCT07001293 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2026-05-07

No results posted yet for this study

Summary

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

  • ADHD
  • Perinatal
  • Behavioral Intervention

Interventions

BEHAVIORAL

MomMA Intervention

The MomMA program is a CBT-based behavioral intervention with components targeted specifically towards expectant parents with ADHD. Treatment will be delivered by therapists embedded in OB care settings.

OTHER

Treatment as Usual (TAU)

Participants will receive treatment as usual, including but not limited to medication and behavioral therapy. No participation in treatment is required.

Sponsors & Collaborators

  • University of Maryland, College Park

    collaborator OTHER

  • University of Pittsburgh

    lead OTHER

Principal Investigators

  • Heather M Joseph, DO Assistant Professor of Psychiatry and Pediatrics · University of Pittsburgh

  • Andrea Chronis-Tuscano, PhD Joel & Kim Feller Endowed Professor · University of Maryland

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-04-26
Primary Completion
2028-05-31
Completion
2028-05-31

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07001293 on ClinicalTrials.gov