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Clinical Trials/KCT0003473
KCT0003473
Recruiting
未知

Development of the Assessment-based tailored psychoeducation and training program for regulation of eMotion and impulse using virtual reality for Suicide Prevention (DAM of Suicide, DAMoS) : Exploratory Clinical Trial

Yonsei University Health System, Gangnam Severance Hospital0 sites60 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Mental and behavioral disorders
Sponsor
Yonsei University Health System, Gangnam Severance Hospital
Enrollment
60
Status
Recruiting
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
7 years ago
Study Type
Observational Study
Sex
All

Investigators

Sponsor
Yonsei University Health System, Gangnam Severance Hospital

Eligibility Criteria

Inclusion Criteria

  • Criteria for selection of clinical trial group and clinical control group
  • 1\) Male and female who have agreed to participate in the study of persons aged 19 years or older and 50 years or younger
  • 2\) Those who score at least 7 points in the PHQ\-9 test in the first\-line online mental health screening evaluation (PHQ\-9\)
  • 3\) Depressive symptom evaluation scale (K\-QIDS\-SR) score of 11 points or more in the second stage in\-depth evaluation
  • 4\) Subjects who reported suicidal tendency score between 2 and 9 in the third step offline precise evaluation.
  • A healthy control group
  • 1\) Male and female who have agreed to participate in the study of persons aged 19 years or older and 50 years or younger
  • 2\) Depression screening test score of less than 5 points in the first stage online mental health screening (PHQ\-9\)
  • 3\) Depressive symptom evaluation scale (K\-QIDS\-SR) score of 5 points or less in the second step in\-depth evaluation
  • 4\) Subjects with a suicidal tendency score of 1 or less in the third step offline precise evaluation.

Exclusion Criteria

  • 1\) Those who have difficulty in using virtual reality (VR) equipment
  • 2\) Subjects who scored below 3 points In the second in\-depth screening evaluation of the basic comprehension capacity.
  • 3\) Subjects who score more than 10 points on the suicidal tendency evaluation score in the third step offline precise evaluation (We are going to provide crisis intervention for these subjects excluding participation in research and recommending psychiatric intensive treatment including medication and psychotherapy.)
  • 4\) Subjects who meet the level of intellectual disability in the short\-form intelligence test (sectioning \& common sense)
  • 5\) Anyone whose risk of suicide is so high that it is difficult to participate in the clinical trial by self\-report or clinician evaluation during the test period is going to be withdrawn, and intensive psychiatric treatment including crisis intervention and medication treatment is carried out.
  • 6\) Subjects with difficulty or limitations in MRI examination (eg, those with claustrophobia, pacemakers, or metallic surgical clips, or cochlear implants, etc.)

Outcomes

Primary Outcomes

Not specified

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