Continuous Assessment for Suicide Prevention And Research (CASPAR): a feasibility study of smartphone-based safety-planning and self-monitoring for suicidal patients in mental health care

Continuous Assessment for Suicide Prevention And Research (CASPAR): a feasibility study of smartphone-based safety-planning and self-monitoring for suicidal patients in mental health care - CASPAR

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON46684

Enrollment

Registered

2018-08-09

Start date

2019-03-28

Completion date

Unknown

Last updated

2024-04-15

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

Conditions

Suicidal ideation

Interventions

We will add two mobile apps to the regular treatment of patients. We will only look at the feasibility of the implementation and we do not have a therapeutic meaning. The CASPAR study is therefore a

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Age * 18 years - Outpatients or day-care patients - Recurrent depressive disorder or dysthymia - Severe suicidal ideation - Understanding written Dutch - Smartphone that runs either Android or iOS

Exclusion criteria

Exclusion criteria: - Severe psychotic symptoms

Design outcomes

Primary

Measure	Time frame
The primary objective is to test the feasibility of the safety planning and self-monitoring tools. Feasibility endpoints are defined in terms of uptake, patient satisfaction and usability.	—

Secondary

Measure	Time frame
Secondary outcomes are the mental health variables measured by the EMA items. These variables include anxiety, belongingness, (brooding) rumination, burdensomeness, fear of dying, coping, defeat, depression, entrapment, future thinking, impulsiveness, resilience and suicidal ideation (see also attachment).	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)