Culturally and Language-Adapted i-CBT for Common Mental Health Problems: A Randomized Controlled Study With Farsi/Dari-Speaking Migrants
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 128
- 试验地点
- 1
- 主要终点
- Hopkins Symptom Checklist-25 (HSCL-25)
研究概览
简要总结
The aim of this randomized controlled trial (RCT) is to investigate the effectiveness of a culturally adapted internet-based cognitive behavioral therapy (i-CBT) intervention in reducing symptoms of common mental health issues among Farsi/Dari-speaking youth migrants and refugees. Investigator hypothesizes that there will be a significant decrease in psychological symptoms after participants receive the intervention compared to a control group.
详细描述
Participants who are included in the study will be allocated to the experimental group and the control group (waiting list). Participants will be invited to participate tailored i-CBT intervention over 10-weeks. Intervention covers common psychological issues. Participants will have access to support through a chatting function, during the interventional period. Intervention effects will be measured prior-treatment, post-treatment, and 6 months post-treatment.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
盲法说明
No masking
入排标准
- 年龄范围
- 15 Years 至 29 Years（Child, Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Between the ages of 15 and
- •A score above the cut-off 1.75 on HSCL-25
- •Has a refugee or migrant background
- •Has a good and stable internet connection
- •Has access to a computer, tablet or smartphone
- •Is fluent in reading and writing Arabic
- •Has the ability to dedicate time to take part in the intervention for 6-10 weeks.
排除标准
- •Is suffering from a severe mental illness, such as psychosis or severe depression.
- •Is suffering from substance abuse
- •Is undergoing a psychological treatment
- •Has a high risk of suicide
研究组 & 干预措施
Active group
Tailored I-CBT for mild to moderate common mental health problems over a 10-weeks-period.
干预措施: Culturally adapted i-CBT (Behavioral)
Waiting-list
Control group
结局指标
主要结局
Hopkins Symptom Checklist-25 (HSCL-25)
时间窗: Pre-intervention, up to 5 weeks, immediately after the intervention, 6 months after completion of the intervention
Assessment of anxiety and depressive symptoms. HSCL-25 consists of 25 items.Each item is rated on a scale from 1 to 4, where 1 means "Not at all" and 4 means "Extremely".Higher scores indicate a worse outcome, as they reflect greater severity of symptoms.
次要结局
- Psychological Outcome Profiles (PSYCHLOPS)(Pre-intervention, immediately after the intervention, 6 months after completion of the intervention)
- Insomnia Severity Index (ISI)(Pre-intervention, immediately after the intervention, 6 months after completion of the intervention)
- Prolonged Grief Disorder (PG-13)(Pre-intervention, immediately after the intervention, 6 months after completion of the intervention)
- Posttraumatic Stress Disorder Checklist (PCL-5)(Pre-intervention, immediately after the intervention, 6 months after completion of the intervention)
- The World Health Organization-Five Well-Being Index (WHO-5)(Pre-intervention, immediately after the intervention, 6 months after completion of the intervention)
- Brief Resilience Scale (BRS)(Pre-intervention, immediately after the intervention, 6 months after completion of the intervention)
- Client Satisfaction Questionnaire (CSQ-3)(Immediately after the intervention, 6 months after completion of the intervention)
研究者
Shervin Shahnavaz
PhD, Lecturer
Karolinska Institutet