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Assessing suicide risk in hospital patients admitted after a suicide attempt using a new screening tool.

Development and pilot testing of a suicide risk assessment proforma for patients admitted in a hospital setting. - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/07/091941
Enrollment
60
Registered
2025-07-29
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: X838- Intentional self-harm by other specified means

Interventions

Intervention1: Nil: Nil

Sponsors

Abel Dani Johnson
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients admitted following a suicide attempt. 2.Patients who are willing to provide informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1.Participants who are unwilling or unable to provide informed consent for participation. 2.Participants with severe physical conditions that preclude their ability to participate in the study or complete the assessment procedures.

Design outcomes

Primary

MeasureTime frame
Identification of key suicide risk factors, protective factors, and facilitation of risk stratification among patients admitted following a suicide attempt.Timepoint: 3 months—

Secondary

MeasureTime frame
Evaluation of the effectiveness and clinical utility of the suicide risk assessment proforma over time through follow-up reassessment to determine whether participants have reattempted suicide or engaged in intentional self-harm.Timepoint: 6 months follow up—

Countries

India

Contacts

Public ContactDr Soyuz John

Kasturba Medical College, Manipal

Soyuz.john@manipal.edu8867604011

Outcome results

None listed

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