跳至主要内容
临床试验/NCT07412548
NCT07412548尚未招募不适用

The Effectiveness of Autogenic Relaxation and Surah Ar-Rahman Murottal Therapy on Anxiety, Sleep Quality, and Hemodynamic Parameters in Hemodialysis Patients

Universitas Muhammadiyah Surakarta1 个研究点 分布在 1 个国家目标入组 76 人开始时间: 2026年3月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
76
试验地点
1
主要终点
Anxiety

研究概览

简要总结

This quasi-experimental study aims to evaluate the effect of combined autogenic relaxation and Surah Ar-Rahman murottal therapy on anxiety, sleep quality, and hemodynamic parameters in hemodialysis patients. A pretest-posttest control group design will be used involving 76 participants undergoing routine hemodialysis. Participants will be assigned to an intervention group receiving structured autogenic relaxation followed by murottal therapy and a control group receiving standard care with music listening. Anxiety, sleep quality, and hemodynamic parameters will be measured at baseline and after a 6-week intervention period. The findings are expected to support the use of non-pharmacological and spiritual-based interventions in improving psychological and physiological outcomes in hemodialysis patients.

详细描述

This study applies a quasi-experimental pretest-posttest control group design. The intervention group receives structured autogenic relaxation followed by Surah Ar-Rahman murottal therapy for 10-15 minutes per session, twice weekly for six weeks. The control group receives standard hemodialysis care with music listening. Anxiety, sleep quality, and hemodynamic parameters are assessed before and after the intervention.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients diagnosed with stage V chronic kidney disease.
  • Undergoing scheduled hemodialysis at least twice a week for 6 weeks.
  • Outpatients and aged 18-65 years.
  • Cooperative and able to communicate verbally.
  • Willing to be a respondent by signing an informed consent form.

排除标准

  • Having a severe heart condition or an unstable critical condition.
  • Having a severe psychiatric disorder (schizophrenia, major depression).
  • Having a cognitive, hearing, or speech disorder that impedes communication.
  • Taking antidepressants, anxiolytics, or neuroleptics that may affect psychological measurement results.

研究组 & 干预措施

Autogenic Relaxation and Murottal Therapy Surah Ar-Rahman

Experimental

Participants in this group receive structured autogenic relaxation followed by Surah Ar-Rahman murottal therapy during hemodialysis sessions. The intervention is administered twice weekly for six weeks, with each session lasting 10-15 minutes. The procedure is conducted by trained nurses under researcher supervision in a quiet and comfortable environment.

干预措施: Autogenic Relaxation and Surah Ar-Rahman Murottal Therapy (Behavioral)

Standard Care

Active Comparator

listening to dangdut music for 10 to 15 minutes within 6 weeks

干预措施: listening to dangdut music (Other)

结局指标

主要结局

Anxiety

时间窗: Baseline and after completion of the 6-week intervention

Change in anxiety level measured using the Zung Self-Rating Anxiety Scale (ZSAS; range 20-80), where higher scores indicate greater anxiety, from baseline to after completion of the 6-week intervention.

Sleep Quality

时间窗: Baseline and after completion of the 6-week intervention.

Change in sleep quality measured using the Pittsburgh Sleep Quality Index (PSQI; range 0-21), where higher scores indicate poorer sleep quality, from baseline to after completion of the 6-week intervention.

Blood Presure

时间窗: Baseline and after completion of the 6-week intervention

Change in systolic blood pressure (mmHg), measured using a calibrated digital sphygmomanometer, from baseline to after completion of the 6-week intervention.

Heart Rate

时间窗: Baseline and after completion of the 6-week intervention

Change in heart rate (beats per minute, bpm), measured using a digital bedside patient monitor, from baseline to after completion of the 6-week intervention.

次要结局

未报告次要终点

研究者

发起方
Universitas Muhammadiyah Surakarta
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dyan Kurniasari

Graduate Researcher

Universitas Muhammadiyah Surakarta

研究点 (1)

Loading locations...

相似试验