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Feasibility of Accessible Video Mental Healthcare Triage and Assessment

NCT06681727 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 172

Last updated 2024-11-19

No results posted yet for this study

Summary

This study aims to describe the immediate psychiatry (IP) service, patient population, and patient flow, as well as investigate the experiences, acceptability, and feasibility of the IP triage service implemented in Region Stockholm, Sweden.

Patients aged 18 years and older who were registered at participating primary care centers were eligible to access the IP through a regional healthcare app. IP comprised a brief digital screening followed by a 45-minute video consultation with a mental health professional. The study will employ a mixed methods design with data from medical records, patient surveys, interviews with the IP team, and clinician acceptability questionnaires. The quantitative data will be analyzed via descriptive statistics, and the qualitative data will be analyzed via content analysis.

Conditions

  • Psychiatric Disorders

Interventions

OTHER

Accessible Video Mental Healthcare Triage and Assessment (IP)

Patients aged 18 years and older who were registered at participating primary care centers were eligible to access the IP through a regional healthcare app. IP comprised a brief digital screening followed by a 45-minute video consultation with a mental health professional. Eligible patients could thereafter schedule appointments at cooperating healthcare centers and clinics through the app used for video consultations.

Sponsors & Collaborators

Principal Investigators

  • Lina Martinsson, MD PhD · Centre for Psychiatry Research, Dept. Clinical Neuro Science. Karolinska Institute

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-12-01
Primary Completion
2023-06-30
Completion
2023-06-30

Countries

  • Sweden

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06681727 on ClinicalTrials.gov