NCT05633940 The Effects of Primary Care Behavioral Health in Primary Care in Sweden
| NCT ID | NCT05633940 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Region Östergötland |
| Condition | Primary Health Care |
| Study Type | INTERVENTIONAL |
| Enrollment | 500 participants |
| Start Date | 2021-01-01 |
| Primary Completion | 2026-12-31 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 500 participants in total. It began in 2021-01-01 with a primary completion date of 2026-12-31.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The novel multi-professional service delivery model "Primary Care Behavioural Health" (PCBH) has been suggested as an effective way to integrate behavioural health services into routine primary care to overcome the growing problems with psychosocial and mental health problems in primary care. In this multicenter mixed-methods pragmatic clinical trial, the implementation of PCBH in routine primary health care in a region in Sweden is investigated.
Eligibility Criteria
Patients: Inclusion Criteria, one of following: * Adult patients who seek care for mental health problems at a participating centre, * Adult patients who have received any following International Classification of Diseases diagnose: F00-F99, Z56, Z73 * Adult patients who are prescribed any psychotropic drugs with ATC codes: N05A-C, N06A) at a participating centre. * Adult patients who has an appointment to a behavioral health consultant at a participating centre. Exclusion Criteria: • Not capable to leave informed consent. Medical staff: Inclusion Criteria: • Health care professionals employed at a participating centre. Exclusion Criteria: • Temporarily hired personnel, e.g. hired doctors or nurses on weekly basis.
Contact & Investigator
Hanna I Larsen, PhD
PRINCIPAL INVESTIGATOR
region östergötland/Primärvårdscentrum/Vårdcentralen Cityhälsan centrum
Frequently Asked Questions
Who can join the NCT05633940 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Primary Health Care. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT05633940 currently recruiting?
Yes, NCT05633940 is actively recruiting participants. Contact the research team at hanna.israelsson.larsen@regionostergotland.se for enrollment information.
Where is the NCT05633940 trial being conducted?
This trial is being conducted at Linköping, Sweden.
Who is sponsoring the NCT05633940 clinical trial?
NCT05633940 is sponsored by Region Östergötland. The principal investigator is Hanna I Larsen, PhD at region östergötland/Primärvårdscentrum/Vårdcentralen Cityhälsan centrum. The trial plans to enroll 500 participants.