Maternal Outcomes: Mood, Alcohol Use, and Depressive Symptoms (NCT07485036)
Maternal Outcomes: Mood, Alcohol Use, and Depressive Symptoms (MOMS-AD Pilot Study)
๐ฉบ Plain-English Summary (8th-Grade Level)
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
Who can join: Review the eligibility criteria below.
Location: University of Illinois Hospital and Health Sciences System, University of Illinois College of Medicine โ Chicago, Illinois
Age range: 18 Years
๐งช Interventions in This Study
- Contingency Management & Problem Solving Therapy (BEHAVIORAL)
- Usual Care (OTHER)
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (1 Sites)
- University of Illinois Hospital and Health Sciences System, University of Illinois College of Medicine โ Chicago, Illinois
๐ Contact the Study Coordinator
Phone: (312) 413-5361
Email: hhalli2@uic.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Postpartum Depression (PPD)
- Living Healthy for Moms RCT โ Brooklyn, New York
- Online Transdiagnostic Group CBT for Postpartum Depression and Anxiety โ Hamilton, Ontario
- SAINT in Postpartum Depression (PPD) โ Worcester, Massachusetts
- Clinical Validation of a Predictive Test for Postpartum Depression โ Charlottesville, Virginia
- A Study of a Test for Postpartum Depression at Home โ Charlottesville, Virginia
Explore by condition: All Postpartum Depression (PPD) clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.