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Think Life, an Online Self-help Intervention for Coping With Suicidal Ideation

A Randomized Controlled Trial on the Effectiveness of an Online Self-help Intervention for Suicidal Ideation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03209544
Enrollment
724
Registered
2017-07-06
Start date
2015-04-23
Completion date
2016-02-24
Last updated
2017-07-06

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

Conditions

Suicidal Ideation

Keywords

Suicidal ideation, Suicide, Cognitive behavioral therapy, Online intervention

Brief summary

The objective of the Think Life study is to test the effect of an online, unguided self-help intervention, i.e. Think Life. The primary hypothesis is that Think Life will reduce suicidal ideation. The secondary hypothesis is that Think Life will lead to improvements in depressive symptoms, hopelessness, rumination, and anxiety. Positive changes are expected after completing Think Life and at follow-up, twelve weeks after baseline.

Interventions

The intervention was originally developed by van Spijker, van Straten, and Kerkhof (2010). For this study, it was adapted to the Flemish context and called Think Life. Think Life is mainly based Cognitive Behaviour Therapy (CBT). Additionally, it encompasses elements from Dialectical Behaviour Therapy (DBT), Problem Solving Therapy (PST), and Mindfulness Based Cognitive Therapy (MBCT). It encompasses six modules and every module starts with a psycho-educational section followed by a weekly assignment, core exercises and optional exercises. The participant weekly receives access to a new module. A more detailed description of the intervention is described elsewhere (Kerkhof, van Spijker, & Mokkenstorm, 2013; van Spijker et al., 2010; van Spijker, van Straten, et al., 2014).

Sponsors

VU University of Amsterdam
CollaboratorOTHER
University Ghent
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Eligibility

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

Inclusion criteria

* 18 years or older * Have internet access and an e-mail account

Exclusion criteria

* No suicidal thoughts (i.e. baseline score on Beck Scale for Suicide Ideation = 0)

Design outcomes

Primary

MeasureTime frameDescription
Beck Scale for Suicide IdeationBaseline, and 2, 4, 6 (post-test) and 12 weeks (follow-up) after baselineChanges in severity of suicidal ideation

Secondary

MeasureTime frameDescription
Suicidal Ideation AttributesBaseline, and 2, 4, 6 (post-test) and 12 weeks (follow-up) after baselineChanges in severity of suicidal ideation
Beck Depression Inventory - second editionBaseline, and 2, 4, 6 (post-test) and 12 weeks (follow-up) after baselineChanges in symptoms and severity of depression
Beck Hopelessness ScaleBaseline, and 6 (post-test) and 12 weeks (follow-up) after baselineChanges in one's negative attitude towards the future
Penn State Worry Questionnaire - Past WeekBaseline, and 6 (post-test) and 12 weeks (follow-up) after baselineChanges in degree of worrying
Hospital Anxiety and Depression ScaleBaseline, and 6 (post-test) and 12 weeks (follow-up) after baselineChanges in anxiety

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026