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A Future-oriented Group Training for Suicidal Patients

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05158946
Enrollment
90
Registered
2021-12-15
Start date
2016-12-08
Completion date
2018-05-31
Last updated
2022-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Suicidal Ideation, Suicide Attempt

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.

Interventions

BEHAVIORALFuture Oriented Group Training

This study's experimental condition consisted of a Future Oriented Group Training (FOGT), originally developed in 2008 by van Beek et al. (2009). Participants followed this training weekly, over a period of 9 weeks in groups of 6 to 10 participants. The sessions, which lasted one and a half hours each, were each led by one trainer.

Sponsors

University Ghent
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Randomized Controlled Trial comparing an experimental condition (Treatment As Usual + Future Oriented Group Training) and a control condition (Treatment As Usual)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Suicidal ideation: The Beck Scale for Suicide IdeationBaseline (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

MeasureTime frameDescription
Depressive symptoms: The second edition of the Beck Depression InventoryBaseline (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 depressive symptoms and attitudes in the past week. Each item is rated on a scale from 0 to 3, resulting in a total score ranging from 0 to 63, with higher scores indicating more depressive symptoms.
Hopelessness: The Beck Hopelessness ScaleBaseline (2 weeks before the intervention), posttest (9 weeks after start of intervention), follow-up (3 months after the end of the intervention)A 20-item self-report questionnaire to measure hopelessness in adolescents and adults. Each item is rated as 'true' (score = 1) or 'false' (score = 0) for them over the past week, resulting in a total score ranging from 0 to 20, with higher scores indicating higher levels of hopelessness.
Defeat: the Defeat ScaleBaseline (2 weeks before the intervention), posttest (9 weeks after start of intervention), follow-up (3 months after the end of the intervention)A 16-item self-report questionnaire to measure defeat on a five-point Likert scale.
Worrying: The Penn State Worry Questionnaire - past weekBaseline (2 weeks before the intervention), posttest (9 weeks after start of intervention), follow-up (3 months after the end of the intervention)A 15-item self-report questionnaire to measure worrying in the past week. Each item is rated on a 7-point Likert scale ranging from 0 (never) to 6 (almost always).
Future-oriented thinkingBaseline (2 weeks before the intervention), posttest (9 weeks after start of intervention), follow-up (3 months after the end of the intervention)A 22-item self-report questionnaire to measure repeated thinking about the future, specifically about the likelihood of negative and positive events happening. Each item is rated on a 4-point Likert scale ranging from 0 (never) to 3 (almost always).
Entrapment: the Entrapment ScaleBaseline (2 weeks before the intervention), posttest (9 weeks after start of intervention), follow-up (3 months after the end of the intervention)A 16-item self-report questionnaire to measure entrapment on a five-point Likert scale.

Other

MeasureTime frameDescription
Treatment evaluationPosttest (9 weeks after start of intervention)Rating of the general training (score ranging from 0 to 10) and 10 statements about several aspects of the format, content and effect of the group training. Of these statements, 4 were rated on a 3-point Likert scale, and 6 on a 5-point likert scale

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026