Implementing digital mobile mental health in routine care

Not Applicable

• Conditions: Mental disorders; Mental and Behavioural Disorders

• Registration Number: ISRCTN15109760
• Lead Sponsor: Central Institute of Mental Health

Brief Summary

2024 Protocol article in https://pubmed.ncbi.nlm.nih.gov/38915006/ (added 25/06/2024)

Detailed Description

Not available

Study Timeline

• Study Start: 2022-08-03
• Last Update Posted: 8 July 2024
• Study Completion: 2025-03-30

Recruitment & Eligibility

• Status: Ongoing
• Sex: All
• Target Recruitment: 532

Inclusion Criteria

Service users:
1. Aged between 14 and 64 years
2. Help-seeking for mental health problems and deemed sufficiently unwell to be accepted for specialist mental health treatment
3. In contact with local inpatient, outpatient, or community mental health services at the participating clinical sites
4. Able to provide informed consent

Clinicians:
1. Providing care and being the clinician in charge of treatment for included service users in one of the clinical units at the participating clinical sites

Exclusion Criteria

Service users:
1. Evidence that psychiatric symptoms are precipitated by an organic cause (incl. a diagnosis of ICD-10 F00-F09)
2. Significant risk to themselves or others
3. Clinical diagnosis of intellectual disability (ICD-10 F70-79) or disorders of psychological development (ICD-10 F80-89) that are sufficiently severe to impair a person’s ability to provide informed consent
4. Medical or psychological contra-indication (as judged by the clinician in charge)
5. Self-reported inability or unwillingness to use a smartphone to collect ESM data
6. Not fluent and literate in German (Germany), Dutch (Belgium), Slovak (Slovakia), or English (Scotland)
7. Short life expectancy/terminal illness

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Patient-reported service engagement measured using the Service Attachment Questionnaire at 2 months