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Investigating the intervention of educational planning in the prevention of repeated suicide attempts in bipolar patients

Investigating the safety planning intervention in preventing repeated suicide attempts in type 1 bipolar patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240621062199N1
Enrollment
96
Registered
2024-08-05
Start date
2024-07-22
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Bipolar disorder. Bipolar disorder

Interventions

Intervention 1: Control group: patients with type 1 bipolar disorder who were admitted to the hospital after attempting suicide and did not receive any training. Intervention 2: Intervention group: pa

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Confirming the diagnosis of bipolar disorder type 1 based on DSM 5 criteria Age range from 18 to 60 years Written consent to participate in the study

Exclusion criteria

Exclusion criteria: Treatment with ECT (Electroconvulsive therapy) in the last 2 months Moderate to severe mental retardation Patients with a known history of dementia and are being treated Existence of a type 1 bipolar disorder, such as anxiety disorders, obsessive-compulsive disorder

Design outcomes

Primary

MeasureTime frame
Suicide. Timepoint: 3 and 6 months after discharge. Method of measurement: Interview.

Secondary

MeasureTime frame
Manic intensity. Timepoint: At the beginning of the study, 3 and 6 months after discharge. Method of measurement: Mania Young Questionnaire.;Depression score. Timepoint: At the beginning of the study, 3 and 6 months after discharge. Method of measurement: Beck depression questionnaire.;Sleep quality score. Timepoint: At the beginning of the study, 3 and 6 months after discharge. Method of measurement: Pittsburgh Sleep Quality Questionnaire.;Drug compliance. Timepoint: 3 and 6 months after discharge. Method of measurement: Interview.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParichehr Golkar

Kerman University of Medical Sciences

parichehrgolkar1990@gmail.com+98 34 3211 1398

Outcome results

None listed

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