Last reviewed · How we verify
NCT05764213
Improving Maternal Mental Health & SUD Screening and Treatment
NA trial testing Listening to Women & Pregnant and Postpartum People in Mental Health Issue in 10,470 participants. Participants enrolled and being followed up; not accepting new ones.
31 July 2027
Quick facts
| Lead sponsor | Medical University of South Carolina |
|---|---|
| Phase | NA |
| Status | Active, enrolled |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | screening |
| Enrollment | 10,470 |
| Start date | 3 April 2023 |
| Primary completion | 31 July 2027 |
| Estimated completion | 1 October 2027 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Listening to Women & Pregnant and Postpartum People
Conditions studied
- Mental Health Issue — all drugs for Mental Health Issue →
- Substance Use Disorders — all drugs for Substance Use Disorders →
- Postpartum Depression — all drugs for Postpartum Depression →
- Postpartum Anxiety — all drugs for Postpartum Anxiety →
Sponsor
Medical University of South Carolina
Who can join
Adults 18 to 45, female only, with Mental Health Issue or Substance Use Disorders. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of the study is to compare a text message-based mental health and substance use screening and referral to a treatment program, called Listening to Women and Pregnant and Postpartum People (LTWP), to standard of care in-person mental health and substance use screening to look at rates of treatment attendance and retention in treatment. Participation would involve completing online questionnaires. You may be eligible to participate if you are age 18-45 years, are pregnant and entering prenatal care in one of MUSC's OB clinics, and attended a prenatal appointment at an MUSC clinic.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT05764213
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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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 NCT05764213 (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 Medical University of South Carolina
- Last refreshed: 8 April 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/NCT05764213.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing