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Clinical Trials/NCT05158946
NCT05158946
Completed
Not Applicable

Randomized Controlled Trial Investigating the Effectiveness of Future-oriented Group Training for Suicidal Patients

University Ghent1 site in 1 country90 target enrollmentDecember 8, 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Suicidal Ideation
Sponsor
University Ghent
Enrollment
90
Locations
1
Primary Endpoint
Suicidal ideation: The Beck Scale for Suicide Ideation
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The main goal of this study is to evaluate the effectiveness of a Future-oriented Group training aimed at reducing suicidality in adults. This will test the effectiveness by studying the effect on suicidal ideation and related outcomes, compared to Treatment As Usual. Participants will also be asked to evaluate the group training. The study is a multicentre randomized controlled trial conducted in out-patient Flemish mental healthcare facilities.

Registry
clinicaltrials.gov
Start Date
December 8, 2016
End Date
May 31, 2018
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Speak Dutch
  • Be at least 18 years old
  • Have access to internet
  • Be suitable for group therapy
  • Have mild to severe suicidal thoughts (BSS score of minimum 1)

Exclusion Criteria

  • Conditions expected to severely hinder group participation, comprehension of the training content or adherence

Outcomes

Primary Outcomes

Suicidal ideation: The Beck Scale for Suicide Ideation

Time Frame: Baseline (2 weeks before the intervention), posttest (9 weeks after start of intervention), follow-up (3 months after the end of the intervention)

A 21-item self-report questionnaire to measure (the severity of) suicidal ideation in adolescents and adults. Each item is rated on a scale from 0 to 2, resulting in a total score ranging from 0 to 38, with higher scores indicating more (severe) suicidal ideation.

Secondary Outcomes

  • Depressive symptoms: The second edition of the Beck Depression Inventory(Baseline (2 weeks before the intervention), posttest (9 weeks after start of intervention), follow-up (3 months after the end of the intervention))
  • Defeat: the Defeat Scale(Baseline (2 weeks before the intervention), posttest (9 weeks after start of intervention), follow-up (3 months after the end of the intervention))
  • Entrapment: the Entrapment Scale(Baseline (2 weeks before the intervention), posttest (9 weeks after start of intervention), follow-up (3 months after the end of the intervention))
  • Worrying: The Penn State Worry Questionnaire - past week(Baseline (2 weeks before the intervention), posttest (9 weeks after start of intervention), follow-up (3 months after the end of the intervention))
  • Future-oriented thinking(Baseline (2 weeks before the intervention), posttest (9 weeks after start of intervention), follow-up (3 months after the end of the intervention))
  • Hopelessness: The Beck Hopelessness Scale(Baseline (2 weeks before the intervention), posttest (9 weeks after start of intervention), follow-up (3 months after the end of the intervention))

Study Sites (1)

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