Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05558891 · ClinicalTrials.gov registry record · NA

Pilot Study of a Brief, Recovery-focused Intervention for Crisis Stabilization Centers

A NA study, sponsored by Centerstone Research Institute.

Completed
Registry status
NA
Development phase
137
Enrollment target

NCT05558891: Completed NA study, sponsored by Centerstone Research Institute.

NCT05558891 is a NA study that has completed, run by Centerstone Research Institute. The registered enrollment target is 137 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05558891, a NA study, has completed, sponsored by Centerstone Research Institute.

COMPLETED
Registry status
NA
Development phase
137 participants
Enrollment target

Study Summary

Crisis Stabilization Centers (CSCs) have a unique role to play in Emergency Department diversion and suicide-specific care. However, brief interventions tailored for CSC settings are needed. This study will examine a new, 60-minute, narrative, technology-based, recovery-oriented intervention called THRIVE. THRIVE may help people make meaning of their suicide crisis, reduce suicidal ideation, and increase their recovery compared to usual care. If effective, THRIVE will help CSCs deliver better recovery-focused care.

Primary Outcome

Integration of Stressful Life Experiences Scale (ISLES; Holland et al., 2010). Subscale scores range from 11 to 55 (Footing in the World subscale), 5 to 25 (Comprehensibility subscale) and 16 to 80 (Total ISLES score). Higher scores on each ISLES subscale and the ISLES total score represent greater meaning reconstruction.

Interventions

  • BEHAVIORAL Usual Care
  • BEHAVIORAL THRIVE

Trial Details

FieldValue
Enrollment Target 137 participants
Start Date 2022-06-22
Est. Completion 2024-06-30
Phase NA
Centerstone Research Institute

2 total trials

What the finished NCT05558891 record still lists

NCT05558891 is an interventional study that assigns participants to a tested intervention. The registered 137 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower).

The record links to 0 conditions, and to 2 interventions - of which Usual Care is the first listed.

NCT05558891 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05558891 about?

NCT05558891 is a clinical study titled "Pilot Study of a Brief, Recovery-focused Intervention for Crisis Stabilization Centers". Crisis Stabilization Centers (CSCs) have a unique role to play in Emergency Department diversion and suicide-specific care. However, brief interventions tailored for CSC settings are needed. This study will examine a new, 60-minute, narrative, technology-based, recovery-oriented intervention called ...

What is the current status of trial NCT05558891?

This trial is currently completed. It is a NA study. The enrollment target is 137 participants. The study started on 2022-06-22. Estimated completion is 2024-06-30.

What interventions are being tested in trial NCT05558891?

The interventions under investigation include: Usual Care (BEHAVIORAL), THRIVE (BEHAVIORAL).

Who is sponsoring clinical trial NCT05558891?

This trial is sponsored by Centerstone Research Institute, which has 2 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05558891's enrollment target sits among peer trials

137 722nd of 2000 higher than 1,279 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT05091424 · 137 participants · Phase 1

    A Study Evaluating the Safety, Efficacy, and Pharmacokinetics of Mosunetuzumab and a Combined Regimen of Mosunetuzumab and Venetoclax in Participants With Relapsed or Refractory Chronic Lymphocytic Leukemia

  • NCT05655182 · 137 participants · Phase 1

    A Study of BLB-201 RSV Vaccine in Infants and Children

  • NCT06571669 · 137 participants · NA

    BOOM-IBD2 Pivotal Clinical Trial

  • NCT06644768 · 137 participants · Phase 1

    A Study of Valemetostat Tosylate Plus Pembrolizumab Versus Pembrolizumab Alone in First-Line NSCLC Without Actionable Genomic Alterations

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT05558891, the US trial registry maintained by the National Library of Medicine. NCT05558891 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.