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Investigating The effectiveness of telenursing training on the suicidal Probability and thoughts of patients and the suicide literacy of caregivers of patients with depression

Investigating The effectiveness of telenursing training on the suicidal Probability and thoughts of patients and the suicide literacy of caregivers of patients with depression admitted to Psychiatric Hospital

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240602061991N1
Enrollment
140
Registered
2024-06-14
Start date
2024-07-22
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Suicidal thoughts, possibility of suicide, suicide health literacy in depressed patients. Suicidal ideations

Interventions

Intervention 1: Intervention group: In the intervention group, in addition to face-to-face training, remote follow-up training (tele-nursing) by the researcher for 8 weeks after discharge from the hos

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: The final diagnosis of the patient at the time of discharge from the hospital is "depression". The degree of depression is "moderate" or "severe". The patient has a history of suicide attempts or thoughts in the past. The patient does not have a history of chronic disease (chronic physical pain, cancer, incurable disease). The patient and caregiver should not have drug addiction and drug use The patient and caregiver have access to a landline or mobile phone The patient and caregiver should have at least reading and writing literacy The patient and caregiver are willing to participate in the study.

Exclusion criteria

Exclusion criteria: The patient or caregiver refuses to continue participating in the study and cooperating with the researcher Failure to answer the phone by the patient or caregiver more than twice The patient or caregiver has sudden accidents such as death or running away from home Occurrence of physical disorders or mental disorders during the study that prevent the patient or caregiver from participating in the sessions.

Design outcomes

Primary

MeasureTime frame
Suicidal thoughts in the Beck questionnaire. Timepoint: Before the start of the intervention, 8 weeks after the start of the intervention. Method of measurement: Beck suicidal ideation questionnaire (BSSI).;Suicide probability. Timepoint: before the start of the intervention and 8 weeks after the start of the intervention. Method of measurement: Cull and Gil suicide probability questionnaire.;Suicide literacy. Timepoint: before the start of the intervention and 8 weeks after the start of the intervention. Method of measurement: LOSS suicide literacy.

Countries

Iran (Islamic Republic of)

Contacts

Public Contact?????? ????????

Mashhad University of Medical Sciences

ebrahimiar@mums.ac.ir+98 915 313 9324

Outcome results

None listed

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