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临床试验/NCT03930225
NCT03930225已完成不适用

Effectiveness of A Stigma Directed Interventional Program in Schizophrenia

Mansoura University1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2019年4月16日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
80
试验地点
1
主要终点
change in Self-Stigma using the Arabic version of the internalized stigma of mental illness scale

研究概览

简要总结

randomized controlled study measuring the effectiveness of Stigma focused intervention in patients suffering from Schizophrenia

详细描述

Effectiveness of A Stigma Directed Intervention Program in Schizophrenia

It is a Randomized Controlled trial that aims at:

  • Assessment of the relationship between self- stigma and
  1. Family burden on the caregiver (Family member).
  2. Medication adherence by patients.
  • Assessment of the effectiveness of the family incorporation in the process of psychoeducation delivered to the patients suffering from Schizophrenia on the self-stigma and family burden of patients with Schizophrenia patients.

The study will be held in Mansoura University hospital Psychiatry department and will include 80 Egyptian patients with Schizophrenia or Schizoaffective disorder will be recruited from Psychiatry department of Mansoura University Hospital

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Outcomes Assessor)

盲法说明

the outcome will be assessed by a different personnel than the investigator conducting the sessions of the intervention. The outcomes assessor will be blinded to which arm each participant belongs.

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Patients meet the diagnosis of schizophrenia or schizoaffective disorder according to DSM5.The clinical condition is stabilized.
  • Age range between 18 to 50 years.
  • Male and female sexes are included.
  • Availability of close relative in direct contact with the patient.
  • Inclusion Criteria for the family members:
  • Primary caregiver and the family member share household with patient.
  • No history of receiving treatment of psychiatric disorders.
  • No history of serious head trauma.

排除标准

  • Co morbid substance abuse or dependence disorder.
  • Co morbid intellectual disability.
  • Co morbid chronic medical or neurological condition or history of serious head trauma.
  • Exclusion Criteria for family members:
  • Sever physical illness that hinders their participation- -

研究组 & 干预措施

study group

Experimental

In the study group, both patients and their family members will be required to attend a weekly 1 hour long psycho-educational sessions. Moreover assessment sessions will be attended also.

"The stigma directed intervention program"

干预措施: Stigma Directed Psycho-educational Intervention program (Behavioral)

control group

Other

In the control group, only Patients will attend the psycho-educational sessions.

Family members and patients will be required to attend the assessment sessions.

干预措施: Stigma Directed Psycho-educational Intervention program (Behavioral)

结局指标

主要结局

change in Self-Stigma using the Arabic version of the internalized stigma of mental illness scale

时间窗: Baseline assessment followed by Point 1 Assessment at the end of the 8 weekly sessions of the program ( after 2 months from baseline assessment) Final assessment after 3 months from point 1 Assessment

stigma as experienced by patients themselves

change in perceived family burden using the perceived family burden scale

时间窗: Baseline assessment---- followed by Point 1 Assessment at the end of the 8 weekly sessions of the program ( after 2 months from baseline assessment) Final assessment after 3 months from point 1 Assessment

how much the disorder represent a burden on family

change in medication adherence using customized chart for each patient

时间窗: Baseline assessment followed by Point 1 Assessment at the end of the 8 weekly sessions of the program ( after 2 months from baseline assessment) fFinal assessment after 3 months from point 1 Assessment

the degree the patient adhere to the prescribed medications

次要结局

  • change in the clinical outcome using Positive and Negative Symptoms Scale(Baseline assessment followed by Point 1 Assessment at the end of the 8 weekly sessions of the program ( after 2 months from baseline assessment) Final assessment after 3 months from point 1 Assessment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Noha Amer

Local Principal Investigator

Mansoura University

研究点 (1)

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