User Evaluation Think Life

Sponsor
University Ghent
Study ID
NCT07654127
Status
Not Yet Recruiting

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Conditions

  • Suicidal Ideation
  • Suicide Prevention
  • mHealth Intervention

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • Self-help course Think Life — OTHER
    Think Life is an online self-help course for individuals experiencing suicidal thoughts, developed by the Flemish Centre of Expertise in Suicide Prevention (VLESP) and offered free of charge via Zelfmoord1813.be. The intervention encompasses six modules, which cover a variety of therapeutic content. Think Life is mainly based on Cognitive Behaviour Therapy (CBT). Additionally, it includes elements from Dialectical Behaviour Therapy (DBT), Problem Solving Therapy (PST), and Mindfulness Based Cognitive Therapy (MBCT). Compared to the original self-help intervention, Think Life constitutes of more CBT elements and less MBCT exercises.The course was originally developed in 2014 and updated in 2025, primarily to improve its look and feel, usability, and inclusiveness, without fundamental changes to its core content.

Study Details

This study aims to evaluate user experiences with the online self-help course Think Life, a suicide prevention intervention for individuals experiencing suicidal thoughts. Think Life was developed by the Flemish Centre of Expertise in Suicide Prevention (VLESP) and is freely available via Zelfmoord1813.be. The course was originally developed in 2014 and updated in 2025 to improve its look and feel, usability, and inclusiveness, without fundamental changes to its core content. The researchers seek to better understand how users experience the updated version of Think Life, including perceived strengths, usability, and overall satisfaction with the course. Users of the Think Life self-help course will be invited through a call displayed on the course homepage to voluntarily participate in an online user evaluation study. Interested individuals can access an online informed consent form via a public internet link hosted on REDCap. Participants who provide online informed consent and meet the inclusion criteria will automatically be redirected to the online questionnaire, which is also hosted on REDCap. Approximately 1000 participants aged 18 years or older can be included in this study. Participants are invited to complete a one-time online questionnaire with an estimated completion time of approximately 10 minutes.

Key Dates

First listed
Jun 17, 2026
Start date
Jun 1, 2026
Status verified
Jun 2026
Primary completion
Jun 1, 2031
Completion
Jun 1, 2031

Study Design

Enrollment
1,000 participants (estimated)

Arms

  • Arm: Study group

Primary Outcome Measure

User evaluation [ Time Frame: Baseline. Completing the questionnaire will take about 10 minutes. ]

Central Contacts

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