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NCT06681727

Feasibility of Accessible Video Mental Healthcare Triage and Assessment

Completed Last updated 19 November 2024
What this trial tests

trial testing Accessible Video Mental Healthcare Triage and Assessment (IP) in Psychiatric Disorders in 172 participants. Completed in 30 June 2023.

Timeline
1 December 2022
Primary endpoint
30 June 2023
30 June 2023

Quick facts

Lead sponsorRegion Stockholm
StatusCompleted
Study typeOBSERVATIONAL
Enrollment172
Start date1 December 2022
Primary completion30 June 2023
Estimated completion30 June 2023
Sites2 locations across Sweden

Drugs / interventions tested

Conditions studied

Sponsor

Region Stockholm — full company profile →

Who can join

18 and older, any sex, with Psychiatric Disorders. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Psychiatric Disorders

Currently open trials in the same condition.

Other Region Stockholm trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing