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Six months follow up study on functioning disability, real world outcome and recovery of participants in depression

A six months follow up of unipolar depression-recovery and dysfunction in a naturalistic prospective study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/10/075579
Enrollment
65
Registered
2024-10-21
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Health Condition 1: F32- Major depressive disorder, singleepisode Health Condition 2: F33- Major depressive disorder, recurrent

Interventions

Control Intervention1: NIL: NIL Control Intervention2: NIL: NIL

Sponsors

Department of Psychiatry
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Any patient with current diagnosis of depressive episode(single episode/recurrent)as per ICD-11. Those who are on adequate doses of antidepressants therapy. Those coming for follow up at the Department of Psychiatry,Kasturba Hospital

Exclusion criteria

Exclusion criteria: Those not able to read English/Hindi/Kannada. Those not willing to consent.

Design outcomes

Primary

MeasureTime frame
The correlation between baseline symptom severity, melancholic symptoms, suicidality and functioning in patients with major depressive episode at 1st,3rd and 6th-month follow-up Timepoint: O,4-6 weeks, 12-14 weeks, 24-28 weeks—

Secondary

MeasureTime frame
The severity of depressive symptoms in patients with major depressive episode at 1st,3rd and 6th-month follow-up in a naturalistic treatment setting. Timepoint: O,4-6 weeks, 12-14 weeks, 24-28 weeks—

Countries

India

Contacts

Public ContactDr Abhiram PN

Kasturba Medical College,Manipal

psvn.sharma@manipal.edu08202922778

Outcome results

None listed

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