Actively Recruiting
Adolescent Depression Treatment Pathways in Primary Care A Longitudinal Cohort Study Describing Naturalistic Flow of Treatment and Evaluating Effectiveness and Cost-effectiveness of Interpersonal Counseling Compared to Treatment as Usual
Led by Finnish Institute for Health and Welfare · Updated on 2025-08-19
9000
Participants Needed
4
Research Sites
708 weeks
Total Duration
On this page
Sponsors
F
Finnish Institute for Health and Welfare
Lead Sponsor
S
Strategic Research Council of Finland
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are conducting a prospective observational cohort study in Finland to evaluate adolescent depression treatment pathways in primary care. The study focuses on adolescents aged 13 to 16 years attending grades 7 to 9 in selected schools, aiming to understand access to treatment and identify those who may benefit from adolescent interpersonal counseling (IPC-A). The study compares IPC-A, a brief behavioral intervention, to treatment as usual and no treatment, assessing effectiveness and cost-effectiveness. The study involves adolescents completing surveys over six months about depressive symptoms, treatment motivation, and benefits or harms from treatment every two weeks. Caretakers will also provide information on adolescent support needs and treatment outcomes through surveys at six-month intervals. When applicable, professionals providing support will report on their training and treatment content. Register data on social welfare and health care service use will be collected from one year before to up to ten years after the study to inform cost and service provision. Participants will be followed for 12 months to measure outcomes including the proportion referred to specialized psychiatric services and changes in depression symptom scores. Data on received support and treatment response will be gathered from adolescents, caretakers, professionals, and patient records. The study will monitor benefits and harms of treatment, aiming to improve detection, equal access, and inform prevention strategies for adolescent depression.
CONDITIONS
Brief Title
Adolescent Interpersonal Counseling in Primary Care
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adolescents attending grades 7 to 9 in selected schools
- Aged between 13 and 16 years
- Informed consent obtained
You will not qualify if you...
- Received psychiatric care or psychosocial intervention in the 12 months before baseline
- Unable to reliably understand Finnish, Plain Finnish, Swedish, or English for survey participation
- Adolescent's or caretaker's report of a medical condition requiring acute treatment or support
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote)
Duration - 6 months
Participants are observed over 6 months to evaluate depressive symptoms and need for support through repeated assessments.
Multiple assessments over 6 months
Duration - Up to 6 months
Participants with sustained depression may receive interpersonal counseling (3 to 8 sessions), treatment as usual, or no treatment based on their needs and preferences.
3 to 8 therapy sessions depending on intervention
Duration - Up to 12 months and longer follow-up up to 10 years
Participants are followed for up to 12 months and beyond to track use of psychiatric and social services and changes in depression symptoms.
Periodic surveys and registry data collection up to 10 years
Trial Site Locations
Total: 4 locations
1
The wellbeing services county of Kanta-Häme
Hämeenlinna, Finland
Actively Recruiting
2
Finnish Institute for Health and Welfare
Helsinki, Finland, 02710
Actively Recruiting
3
The wellbeing services county of Central Finland
Jyväskylä, Finland
Actively Recruiting
4
The wellbeing services county of North Ostrobothnia
Oulu, Finland
Actively Recruiting
Research Team
O
Outi Linnaranta, MD, PhD
J
Jasmin Kaljadin, MSc
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here