Last reviewed · How we verify
NCT05832424
Feasibility and Acceptability of a Telehealth Intervention Among Women With Perinatal Mental Health
NA trial testing UPLIFT program in Perinatal Depression in 30 participants. Status unknown.
22 January 2025
Quick facts
| Lead sponsor | Boise State University |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | prevention |
| Enrollment | 30 |
| Start date | 15 March 2024 |
| Primary completion | 22 January 2025 |
| Estimated completion | 22 January 2025 |
Drugs / interventions tested
- UPLIFT program
Conditions studied
- Perinatal Depression — all drugs for Perinatal Depression →
- Perinatal Anxiety — all drugs for Perinatal Anxiety →
- Substance Use — all drugs for Substance Use →
- Telehealth — all drugs for Telehealth →
Sponsor
Boise State University
Who can join
18 and older, female only, with Perinatal Depression or Perinatal Anxiety. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The goal of this pilot feasibility/acceptability study is to evaluate the effectiveness of a telehealth approach to increase access to services and reduce depression/anxiety symptoms and risk of substance use in a population of women with perinatal depression/anxiety and elevated substance use risk. The main questions it aims to answer are: * Assess the acceptability and feasibility of a telehealth approach to deliver an 8-week evidence-based group intervention to women with perinatal depression/anxiety and mild to moderate substance use risk. * Obtain preliminary data on treatment response to a telehealth 8-week evidence-based group intervention. Participants will participate in an 8-week evidence-based group intervention and complete the study questionnaire including depression severity, treatment adherence, and substance use risk which will be evaluated at baseline, post-intervention, and 2-month follow-up.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT05832424
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
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Related trials
Other recruiting trials for Perinatal Depression
Currently open trials in the same condition.
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- NCT06364488 — TrueBlue Clinical Study - Investigating the Use of a Mobile Phone App TrueBlue for Monitoring Depression and Anxiety · NA · recruiting
- NCT06473935 — Maternal Well-being in the Perinatal Period · recruiting
Other Boise State University trials
Trials by the same sponsor.
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- NCT05925868 — The Mental Health Effects of a Mindfulness App in Parents of a Child With Medical Complexity · NA · completed
- NCT06002347 — Middle School Parent Module for a Brief Bullying Intervention Program · NA · completed
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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 NCT05832424 (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 Boise State University
- Last refreshed: 14 February 2024
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/NCT05832424.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing