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Efficacy of psychoeducation in the treatment of unipolar depression

Efficacy of psychoeducation in the treatment of unipolar depression: a multicentric randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN10760801
Enrollment
120
Registered
2009-04-30
Start date
2009-05-01
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

Unipolar depression in adults Mental and Behavioural Disorders Depressive episode

Interventions

The subjects in the experimental group will receive an 8-week course on psychoeducation based on Lewinsohn's Coping With Depression Course combined with treatment as usual (TAU). The subjects in the c

Sponsors

Clinical Centre University of Sarajevo (Bosnia and Herzegovina)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Adult subjects aged 18 to 65 years, either sex 2. Diagnosis of unipolar depression (F 32.0-2, F 33.0-2) 3. Not due to a medical condition (Diagnostic and Statistical Manual of Mental Disorders, 4th Edition [DSM IV] Axis V = 0) 4. No other Axis I co-morbid psychiatric disorder 5. Duration of symptoms not less than 3 months 6. Able to read and write (8 years formal education) 7. Subjects who sign the informed consent to participate in the study

Exclusion criteria

Exclusion criteria: 1. Refused to sign informed consent 2. Illiterate 3. Deaf or hearing impaired 4. Serious speech impairment or mutisim 5. Duration of symptoms less than three months 6. Symptoms of psychotic depression 7. History of a manic or hypo-manic episode 8. Cognitive impairment (mini Mental State Examination [MMSE] greater than or equal to 25) 9. Co-morbid anxiety disorder 10. Organic affective disorder 11. Depression caused by an underlying medical condition 12. Co-morbid personality disorder 13. Alcohol and preliminary alcohol screening (PAS) abuse and dependence 14. Subjects who are currently involved in other research 15. Pregnancy 16. Epilepsy 17. Subjects whose present condition requires psychiatric hospitalisation 18. Suicidality

Design outcomes

Primary

MeasureTime frame
To assess possible changes in the total score on Beck Depression Inventory scale (BDI), and Hamilton Depression Scale (HAM-D), between the subjects who received psychoeducation and treatment as usual and the subjects who received only treatment as usual, after a 12 week course of psychoeducation, and in 9 months follow-up.

Secondary

MeasureTime frame
1. To assess possible changes in the total score on Manchester Quality of Life Scale (MANSA) between the subjects who received psychoeducation and treatment as usual and the subjects who received only treatment as usual, after a 12 week course of psychoeducation and in 9 months follow-up 2. To assess possible differences in types of mental health services received between the two groups in 9 months follow-up

Countries

Bosnia and Herzegovina

Outcome results

None listed

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