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临床试验/NCT07833982
NCT07833982尚未招募不适用

Efficacy of an Integrated Psychological Interventions Combined With Ar_Rahman Listening for Reducing Psychological Distress and Enhancing Hope and Quality of Life Among Cancer Patients: A Randomized Controlled Trial

Shaheed Zulfikar Ali Bhutto Institute of Science and Technology (SZABIST) University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年9月15日最近更新:
适应症
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
60
试验地点
1
主要终点
psychological distress (DASS-21)

研究概览

简要总结

This is a randomized control trial(RCT ID:25142101) to evaluate the efficacy of psychological intervention combined with listening to surah Ar- RAhman for reducing psychological distress and improving cancer patients' hope and overall QOL compare to standard care. participants will be randomly assigned to two groups: intervention group will receive 14-sessions based manualized psychotherapy plus daily listening to surah Ar- rehman for 12 weeks, and control group will receive standard care .psychological distress will be measured with DASS-21, Quality of Life (QLQ-C30) for assessing Quality of life and Adult hope scale for assessing hope before and after the intervention.

详细描述

this is a two- arm parallel randomized control trial. Background: psychological distress is common in cancer patients and affects treatment outcomes. spiritual and religious interventions, particularly, listening to QURAN recitation(Surah Ar Rahman), have shown potential to reduce anxiety and depression giving hope anf improving overall QOL.

objective

To determine the effectiveness of psychological intervention combined with Surah Ar Rahman listening in reducing psychological distress and enhancing hope and Quality of Life in cancer patients Methods: approximately 60 adults cancer patients will be recruited and randomized(1:1) into intervention and control groups. intervention group: 8 weekly psychological counseling session (30-45 min) based on supportive psychotherapy and CBT techniques plus listening to surah Ar Rahman recitation by Qari Abdul Basit (20 min daily). control group : Standard medical care and general information. assessment at pre and post intervention .

研究设计

研究类型
Interventional
分配方式
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

  • Inclusion Criteria
  • Aged 18 years or older
  • Have a confirmed diagnosis of cancer stage I and II will be included to obtain a relatively comparable clinical population and reduce variability associated with advanced disease and palliative care needs.
  • Are currently receiving or have received cancer-related treatment, such as chemotherapy, radiotherapy, surgery, immunotherapy, or other oncological treatment.
  • Education level will be matric atleast
  • Muslim patients
  • Able to communicate and provide consent

排除标准

  • • Severe psychiatric disorders
  • Cognitive impairment
  • Hearing impairments preventing audio participation
  • Physically unfit for this study's interventions (for example who are bed-bonded or too weak to engage in the study interventions)

研究组 & 干预措施

intervention group

Experimental

participants will receive 12 week of psychological intervention weekly(30-45 min) counseling based supportive therapy plus daily listening to surh Ar Rahman recitation (Qari abdul basit, 20 min) via audio player.

干预措施: supportive psychotherapy plus QURAN recitation9Surah Ar -Rahman (Behavioral)

control group

No Intervention

participants will receive standard oncological care and general health information without psychological intervention or QURAN recitation

结局指标

主要结局

psychological distress (DASS-21)

时间窗: baseline and 12 weeks post intervention

Psychological distress will be measured using DASS-21, a 21 item self-report instrument with 3 subscales: Depression (7 items) Anxiety(7 items) and stress(7 items). each item is scored on 0-3 Likert scale. total score range is 0-63, Scores of each subscale are categorized into five severity ranges: Normal, mild, moderate, severe and extremely severe. For depression normal range(0-9), mild(10-13), Moderate(14-20), Severe(21-27), Extremely severe(28+), for anxiety normal range(0-7), mild(8-9), Moderate(10-14), Severe(15-19), Extremely severe(20+),for stress normal range(0-14), mild(15-18), Moderate(19-25), Severe(26-33), Extremely severe(34+) While the scores do not provide a functional diagnosis, they indicate the potential presence of depression, anxiety, and stress

次要结局

  • Quality of Life -EORTC QLQ-C30(Baseline and 12 week post-intervention)
  • Adult Hope scale(AHS)(baseline and 12 weeks post intervention)

研究者

发起方
Shaheed Zulfikar Ali Bhutto Institute of Science and Technology (SZABIST) University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Mobeen Mehmood

Principal investigator/PhD Scholar

Shaheed Zulfikar Ali Bhutto Institute of Science and Technology (SZABIST) University

研究点 (1)

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