Experience Sampling in patients and their partners at an emergency psychiatry service; a pilot study.

• Conditions: psychothology; suicidality; 10042460

• Registration Number: NL-OMON49413
• Lead Sponsor: Arkin (Amsterdam)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 15 April 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 30

Inclusion Criteria

Population
15 patients who are referred to our department because of suicidal thoughts or
behavior and accepted for out-patient treatment and their 15 live-in partners
will be enrolled upon the start of treatment.

criteria for all 30 participants:
- To be mentally competent to decide about participating in the study
- Written informed consent has been provided
- Mastery of Dutch Language in speech and writing;
- In possession of an electronic device, e.g. smart-phone, i-pad, which
supports the PsyMate app;
- Ability to use the PsyMate app and comply with the study protocol (clinical
judgment treating physician).

Exclusion Criteria

- Participation in another study that is ongoing at our department;
- Homelessness;
- Primary addiction problem

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Primary study parameters/ endpoints will be:<br /><br>1)The number and percentage of participants completing the study;<br /><br>2) the percentage of PsyMate beeps followed (i.e. questionnaires filled out)<br /><br>per participant;<br /><br>3) the participants* experiences with the PsyMate.<br /><br>The secondary endpoints will be the outcomes on the test-battery, and daily ESM<br /><br>questionnaires. </p><br>