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Information technology in the out-patient care of adolescents with depression

Evaluation of information technology in the out-patient care of adolescents with depression: a multicentre randomised controlled trial with two arms

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN80379583
Enrollment
300
Registered
2010-01-07
Start date
2008-11-17
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression, out-patient care Mental and Behavioural Disorders Depressive episode

Interventions

Intervention group: Adolescents in intervention group participate to one face-to-face session with researcher where they receive information on intervention, username and password to Depis.Net e-lear
family life
adolescents' depression and adolescents' rights and duties. In addition, Depis.Net -platform includes reflective diary, question corner, BDI-21 questionnaire, reflective questions, network map, and sc
baseline, follow up at 3, 6 and 12 month.

Sponsors

Academy of Finland (Finland)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Adolescents contacting psychiatric out-patient clinics at study hospitals 2. Aged 15 - 17 years, either sex 3. Ability to read, write and speak Finnish 4. Voluntary participation and written consent form

Exclusion criteria

Exclusion criteria: 1. Psychotic depression, bipolar disorder, substance abuse 2. Admission to psychiatric in-patient care 3. No depressive symptoms (21-item Beck Depression Inventory [BDI-21] = 10 or under 10) 4. Less than three therapy sessions planned

Design outcomes

Primary

MeasureTime frame
Depressive symptoms: BDI-21. Data collection will take 12 months at four points: baseline, and 3, 6, and 12 months follow-up from baseline.

Secondary

MeasureTime frame
1. Behaviour disorders: The Strengths and Difficulties Questionnaire (SDQ). Data collection will take 12 months at four points: baseline, and 3, 6, and 12 months follow-up from baseline. 2. Psychosocial functioning; data collection will take 12 months at four points: baseline, and 3, 6, and 12 months follow-up from baseline: 2.1. The Global Assessment Scale (cGAS) 2.2. Clinical Global Impressions (CGI) Data collection will take 12 months at four points: baseline, and 3, 6, and 12 months follow-up from baseline. 3. Knowledge about illness and treatment: Knowledge test (ADKQ). Data collection will take 12 months at four points: baseline, and 3, 6, and 12 months follow-up from baseline. 4. Satisfaction with treatment: ADTSQ. Data collection will take 12 months at four points: baseline, and 3, 6, and 12 months follow-up from baseline. 5. Quality of Life: PQ-LES-Q. Data collection will take 12 months at four points: baseline, and 3, 6, and 12 months follow-up from baseline. 6. Costs: Client Services Receipt Inventory (CSRI): questions concerning use of health care resources for a retrospective period of 3 months (administered at baseline and 12 month follow-up only)

Countries

Finland

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026