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NCT07072845: E-BCBT
Enhanced Brief CBT for Suicidal Inpatients With Mood Disorders
NA trial testing Enhanced Brief Cognitive Behavioral Therapy (E-BCBT) for Suicidal Inpatients in Suicidal Ideation and Behaviors in 30 participants. Enrolling by invitation.
22 April 2026
Quick facts
| Lead sponsor | Hyung Keun Park |
|---|---|
| Phase | NA |
| Status | ENROLLING BY INVITATION |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 30 |
| Start date | 30 July 2025 |
| Primary completion | 22 April 2026 |
| Estimated completion | 22 April 2026 |
| Sites | 1 location across South Korea |
Drugs / interventions tested
- Enhanced Brief Cognitive Behavioral Therapy (E-BCBT) for Suicidal Inpatients
- Treatment as Usual (TAU) — full drug profile →
Conditions studied
- Suicidal Ideation and Behaviors — all drugs for Suicidal Ideation and Behaviors →
- Suicide Attempt — all drugs for Suicide Attempt →
- Cognitive Behavioral Therapy — all drugs for Cognitive Behavioral Therapy →
Sponsor
Hyung Keun Park
Who can join
18 and older, any sex, with Suicidal Ideation and Behaviors or Suicide Attempt. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The goal of this clinical trial is to evaluate whether enhanced brief cognitive behavioral therapy (E-BCBT) can help reduce suicidal thoughts and behaviors among psychiatric inpatients. This therapy is designed to be feasible during hospitalization and includes self-directed worksheets that may later be used independently after discharge, offering potential benefits for suicide prevention outside the hospital setting as well. Participants will be randomly assigned to one of two groups: * E-BCBT group: Participants will receive five sessions of cognitive behavioral therapy (approximately 50-60 minutes each) during their inpatient stay. * TAU (treatment as usual) group: Participants will receive standard care provided on the psychiatric ward. All participants will take part in five assessments: one before treatment, one after treatment, and three monthly follow-up assessments over the three months after discharge. Assessments include interviews, conducted in person or by phone, and questionnaires, completed online via a survey link. The entire study period will take approximately four months.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT07072845
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Hyung Keun Park trials
Trials by the same sponsor.
- NCT07395817 — Video Conference-Based Brief Cognitive Behavioral Therapy for Suicidal High-Risk Outpatients With Mood Disorders · NA · 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 NCT07072845 (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 Hyung Keun Park
- Last refreshed: 3 October 2025
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/NCT07072845.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing