跳至主要内容
临床试验/CTRI/2024/03/064506
CTRI/2024/03/064506招募中4 期

Efficacy of a co-designed brief contact and outreach intervention in attempted suicide: A Randomized Controlled Trial

Jawaharlal Institute of Postgraduate Medical Education and Research1 个研究点 分布在 1 个国家目标入组 362 人开始时间: 2024年7月31日最近更新:

试验速览

阶段
4 期
状态
招募中
入组人数
362
试验地点
1
主要终点
Increase in time to occurrence of first repeat suicide related event (occurrence of significant suicidal ideation, hospitalization for suicide related reasons, actual suicide attempt, interrupted attempt, or suicide)

研究概览

简要总结

An initial brief Intervention during first contact and further sustained contact attempts at regular intervals could prove to be beneficial in reducing repeat suicide attempts. Hence, the current study aims to assess the efficacy of a brief contact and mHealth based intervention in reducing reattempts and suicidal ideation. The study will also assess the efficacy of the intervention in reducing depressive symptoms, functioning and in improving coping mechanisms of individual.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 99.00 Year(s)(—)
性别
All

入选标准

  • Patients with suicide attempts, confirmed using Columbia-Suicide Severity Rating Scale (C-SSRS), aged 18 years and above with access to mobile phones, admitted to the hospital and visiting Psychiatry department.

排除标准

  • People with suicide attempts who are medically unstable, those who have known bipolar disorder or schizophrenia or are unable to give consent or those who refuse to participate.
  • Patients with BPD and schizophrenia will also be excluded based on diagnosis by a qualified psychiatrist.

结局指标

主要结局

Increase in time to occurrence of first repeat suicide related event (occurrence of significant suicidal ideation, hospitalization for suicide related reasons, actual suicide attempt, interrupted attempt, or suicide)

时间窗: At baseline | At three months | At nine months | At eighteen months | At study endpoint

次要结局

  • Reduction in depressive symptoms(Improvement in coping)

研究者

申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr Vikas Menon

Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER)

研究点 (1)

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