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临床试验/NCT07833449
NCT07833449已完成不适用

The Effect of Murottal Quran on Fatigue Severity Scale and Shatri-Sinulingga Psychosomatic Test Scores in Patients With Human Immunodeficiency Virus Experiencing Psychosomatic Symptoms and Fatigue: A Randomized Controlled Trial

Universitas Indonesia1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年5月20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
60
试验地点
1
主要终点
Change in Shatri-Sinulingga Psychosomatic Test (SSPT) Score

研究概览

简要总结

This randomized controlled trial evaluates the effect of Quranic recitation (murottal) on psychosomatic symptoms and fatigue in adults living with HIV who have psychosomatic symptoms and fatigue. Participants are randomly assigned to either the intervention group, which receives Quranic recitation for approximately 15 minutes, three times per week for 30 days, or the control group. Psychosomatic symptoms and fatigue are assessed before and after the intervention using the Shatri-Sinulingga Psychosomatic Test (SSPT) and Fatigue Severity Scale (FSS), respectively.

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

入排标准

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

入选标准

  • Adults aged ≥18 years. Diagnosed with human immunodeficiency virus (HIV) infection. Muslim. HIV clinical stage 1-
  • Undetectable HIV viral load. Shatri-Sinulingga Psychosomatic Test (SSPT) score ≥
  • Fatigue Severity Scale (FSS) score ≥
  • Willing to participate in the study and provide informed consent.

排除标准

  • Severe hearing impairment or inability to follow the intervention procedure. Psychotic disorder or depressive disorder requiring psychiatric medication. Pregnancy. Active opportunistic infection. Refusal to participate in the study.

研究组 & 干预措施

Murottal Quran

Experimental

15 mins/ 3 times a week for 30 days

干预措施: Quranic Recitation (Murottal) (Behavioral)

Control

No Intervention

Standard care without murottal intervention

结局指标

主要结局

Change in Shatri-Sinulingga Psychosomatic Test (SSPT) Score

时间窗: Baseline to 30 days after randomization

Change in Fatigue Severity Scale (FSS) Score

时间窗: Baseline to 30 days after randomization

次要结局

未报告次要终点

研究者

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

Desty Gusti Sari

Internal Medicine Specialist / Internal Medicine Resident (PPDS)

Universitas Indonesia

研究点 (1)

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