Last reviewed · How we verify
NCT07485036: MOMS-AD
Maternal Outcomes: Mood, Alcohol Use, and Depressive Symptoms
NA trial testing Contingency Management & Problem Solving Therapy in Postpartum Depression (PPD) in 30 participants. Not yet recruiting.
30 May 2027
Quick facts
| Lead sponsor | University of Illinois at Chicago |
|---|---|
| Phase | NA |
| Status | Not yet recruiting |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 30 |
| Start date | 27 February 2026 |
| Primary completion | 30 May 2027 |
| Estimated completion | 30 November 2027 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Contingency Management & Problem Solving Therapy
- Usual Care
Conditions studied
- Postpartum Depression (PPD) — all drugs for Postpartum Depression (PPD) →
- Alcohol Use — all drugs for Alcohol Use →
- Contingency Management — all drugs for Contingency Management →
- Problem Solving Therapy — all drugs for Problem Solving Therapy →
Sponsor
University of Illinois at Chicago
Who can join
18 and older, female only, with Postpartum Depression (PPD) or Alcohol Use. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study aims to learn about depression and alcohol use in postpartum mothers and whether an intervention based on contingency management and problem-solving therapy (CM-PST) can help reduce these symptoms. The main questions it seeks to answer are: 1. How do new mothers fare with depressive symptoms and alcohol use in the first 12 months after giving birth? 2. Will a CM-PST intervention reduce depressive symptoms and alcohol use frequency among new mothers? 3. Is a CM-PST intervention practical for new mothers? The researchers will recruit approximately 30 new mothers and randomly select half to attend a 6-week CM-PST intervention. They will compare those who received the intervention versus those who did not to see if there are any differences in their depressive symptoms and alcohol usage. Participants will: * Complete 4 remote intervention sessions over 6 weeks * Conduct at-home urine drug tests 2x per week during the 6-week intervention * Answer online surveys about their mental health and alcohol use
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT07485036
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Postpartum Depression (PPD)
Currently open trials in the same condition.
- NCT07384273 — Evaluating the Effectiveness of an Internet-based Therapy (iCARE) to Treat Symptoms of Postpartum Depression · NA · recruiting
- NCT07210255 — SAINT in Postpartum Depression (PPD) · NA · recruiting
- NCT07077759 — An Online Self-compassion Intervention for Anxiety and Depression in Fathers of Infants: A Feasibility Study · NA · active not recruiting
- NCT07272252 — Narrative Nursing for Cesarean Mothers' Anxiety and Breastfeeding Confidence · NA · recruiting
- NCT07300176 — Virtual Reality-Assisted Intraoperative Sensory Modulation on Postpartum Depression and the Kynurenine Pathway · active not recruiting
Other University of Illinois at Chicago trials
Trials by the same sponsor.
- NCT07498322 — Chicago Data-driven Opioid Use Disorder Screening, Engagement, Treatment and Planning System · NA · not yet recruiting
- NCT07387705 — On Track for Wellness (OTW) Stepped Wedge Cluster Randomized Trial · Phase 1 · not yet recruiting
- NCT07504120 — The Effect of Remotely Delivered Pilates on Physical , and Psychological Outcomes in Individuals With Multiple Sclerosis · NA · not yet recruiting
- NCT07160582 — Cognitive-Motor Training for AD/ADRD Prevention · NA · not yet recruiting
- NCT07498348 — Apple Watch Evaluation of Endodontics Occupational Stress · not yet recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07485036 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University of Illinois at Chicago
- Last refreshed: 20 March 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07485036.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing