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Clinical Trials/DRKS00014426
DRKS00014426
Completed
未知

Web-based preventive group intervention for persons bereaved by suicide: A randomized control group trial - GROUP-CARE

Medical School Berlin0 sites159 target enrollmentApril 12, 2018

Overview

Phase
未知
Intervention
Not specified
Conditions
suicidalitybereavement, grief
Sponsor
Medical School Berlin
Enrollment
159
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 12, 2018
End Date
June 2, 2021
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
Medical School Berlin

Eligibility Criteria

Inclusion Criteria

  • experienced loss of the suicide of a close person
  • \- Men and women
  • \- Adults between 18 and 75 years
  • \- Access to the Internet
  • \- German language skills
  • \- signed consent form
  • \- Currently not in psychotherapy

Exclusion Criteria

  • 1\) Acute Suicidality: Suicidality is assessed in the telephone interview using the Suicide Risk Assessment Interview (SRAI; Arnoldi, Van de Ven, Schrieken, \& Lange, 2000; Knaevelsrud, 2005\). If potential participants express acute suicidality, they will be excluded from the treatment. In addition, the suicide item of the Beck\-Depression\-Inventaroy (BDI\-II; Hautzinger et al., 2006\) is considered separately in the weekly after\-session\-measurements. The answer options of the item are: 1\) I do not think about doing anything to me; 2\) I sometimes think of suicide but would not do it; 3\) I would like to kill myself; 4\) I would kill myself if I had the opportunity. If participants indicate any other option than option 1\), a telephone appointment will be arranged and a separate suicide screening will be conducted, which will check the concreteness and quality of the suicidal thoughts.
  • 2\) Increased Depressiveness: Participants who have a BDI\-II score of \> 35 are excluded from the treatment.
  • 3\) Psychotic Experience: Participants with a cut\-off score \> 13 in the Dutch Screening Device for Psychotic Disorder (SDPD; Knaevelsrud, 2005; Lange, Schrieken, Blankers, Van de Ven, \& Slot, 2000\) are excluded from the study.
  • 4\) Increased Alcohol, Drug, or Substance Use: Measured by the biographical questionnaire and the Structured Clinical Interview for DSM\-IV Achse I (SKID\-I; Wittchen, Zaudig, \& Fydrich, 1997\).
  • 5\) Persons already in psychotherapeutic treatment: Measured using the biographical questionnaire.
  • 6\) Borderline personality disorder and/or self\-injurious behavior: Measured by the Structured Clinical Interview for DSM\-IV Axis II (SKID\-II; Wittchen et al., 1997\)
  • 7\) Bipolar disorder: Measured by the SKID\-I.

Outcomes

Primary Outcomes

Not specified

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