Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
Healthy Volunteers
ID03846375

Emotional Dysregulation in Para-suicidal Behavior: Effects of Dialectical Behavioral Therapy on Emotional Processing, a Triangulation Approach

Led by Haukeland University Hospital · Updated on 2019-08-28

60

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

Sponsors

H

Haukeland University Hospital

Lead Sponsor

U

University of Bergen

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are investigating the emotional processing changes related to the treatment of non-suicidal self-injury and suicidal thoughts using Dialectical Behavior Therapy (DBT). This study explores how DBT affects emotion regulation, intensity and frequency of self-harm and suicidal ideation, and includes measurements of anxiety, depression, and impulsivity as common related conditions. A matched control group of healthy individuals is included for comparison. Participants receiving DBT will undergo a standard outpatient program focused on improving emotion regulation skills, which is a manualized therapy addressing maladaptive behaviors like self-injury and suicidal thoughts. The study uses a naturalistic pre-post design with assessments at baseline, week 16, week 32, and upon completion of the approximately one-year DBT program. Healthy controls complete baseline testing only. Throughout the study, participants will complete self-report questionnaires on emotion regulation, mindfulness, self-compassion, anxiety, depression, and impulsivity, alongside psychophysiological testing including heart rate variability to measure emotional regulation capacity. The primary outcomes assessed include changes in suicidal thoughts, self-injury frequency, impulse intensity, and heart rate variability. Data will be analyzed to understand how emotion regulation improves with DBT and how these changes relate to clinical improvements over time.

CONDITIONS

Brief Title

Emotional Dysregulation in Para-suicidal Behavior

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with non-suicidal self-injury and/or suicidal ideation who are undergoing standard outpatient Dialectical Behavior Therapy (DBT) treatment
  • Aged between 18 and 65 years
  • Able to provide informed consent
Not Eligible

You will not qualify if you...

  • Lack of informed consent
  • For healthy controls: former or current neurological conditions
  • For healthy controls: severe psychiatric illness
  • For healthy controls: cardiac conditions

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Pre-intervention Testing

Duration - 1 day

Participants complete baseline assessments including clinical, cognitive, and psychophysiological measures before starting therapy.

1 visit (in-person)

Outpatient Treatment

Duration - Approximately 1 year

Participants receive standard Dialectical Behavior Therapy (DBT) aimed at improving emotion regulation and reducing self-harm and suicidal ideation.

Regular therapy sessions over the treatment period

Follow-up Assessments

Duration - Up to 1 year from baseline

Participants complete follow-up assessments to measure changes in suicidal thoughts, self-injury behaviors, emotion regulation, and related symptoms.

Assessments at week 16, week 32, and at treatment completion

Trial Site Locations

Total: 1 location

1

Haukeland University Hospital, Bjørgvin DPS

Bergen, Norway, 5009

Actively Recruiting

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Research Team

B

Berge Osnes, PhD

L

Lin Sørensen, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

2

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