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Brief DBT Skills Training for Coping With Suicidal Ideation

NCT07039058 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2025-09-08

No results posted yet for this study

Summary

The goal of this clinical trial is to learn if Brief Dialectical Behavior Therapy Skills Training (DBT-BST) can prevent suicidality in adults. The main questions it aims to answer are:

* Does DBT-BST provide coping strategies (e.g., emotion regulation) to participants with suicidal ideation?
* Does DBT-BST lower participants' suicide ideation?

Researchers will compare DBT-BST to relaxation to see if DBT-BST works to reduce suicidal ideation.

Participants will:

* Receive DBT-BST in a single 60-minute, in-person, individual session.
* Be asked to use these skills as self-help and for crisis prevention.

Conditions

  • Suicide Ideation
  • Coping Skills
  • Emotion Regulation

Interventions

BEHAVIORAL

Brief Dialectical Behavior Therapy-Skills Training

The intervention is administered in a single session, lasting approximately 60 minutes and conducted in person. It is important to note that there are no ongoing sessions. In the intervention, participants are provided with 5 basic skills of Dialectical Behavior Therapy: 1) mindfulness, 2) mindfulness of current emotions, 3) opposite-to-emotion action, 4) distraction, and 5) changing body chemistry. These strategies are grouped under 3 categories: 1) Mindfulness, 2) Emotion regulation (mindfulness of current emotions, opposite-to-emotion action), 3) Tolerating distress (distraction, changing body chemistry). These skills are not designed to treat or solve the crisis. The main aim is to provide effective coping mechanisms that can be implemented quickly before the crisis escelates, to help overcome the intense emotional pain and keep the person alive.

BEHAVIORAL

Relaxation

The control group will be subjected to a relaxation exercise, with the objective of managing participant expectations, researcher attention/interest, and time spent, as well as providing a coping strategy for stress.

Sponsors & Collaborators

  • Muhammed Ali Boztepe

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-10-31
Primary Completion
2026-01-31
Completion
2026-01-31

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07039058 on ClinicalTrials.gov