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Not yet recruitingNCT07833982Updated Sep 22, 2026

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

An interventional study of supportive psychotherapy plus QURAN recitation9Surah Ar -Rahman in Psychological Distress (Depression, Anxiety and Stress) Cancer, sponsored by Shaheed Zulfikar Ali Bhutto Institute of Science and Technology (SZABIST) University. Not yet recruiting at 1 site in Pakistan. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-09-22.

Sponsored by Shaheed Zulfikar Ali Bhutto Institute of Science and Technology (SZABIST) University · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-13

Among 81 studies in Depression with a site in Pakistan — 23 open to participants now, 29 under way, none of them phase 3. Depression · Pakistan.

Planned enrollment
55th of 76
60 · median 101
Started
2026
with 10 others
No phase
74 of 81
21 open now
Primary completion
2027-11
later than 26 of 28 live
Registered
81st of 81
by date

Among the 81 studies in Depression with a site in Pakistan, this one is the 55th largest by planned enrollment of the 76 interventional ones that give a count, is one of 11 that started in 2026, is one of 74 with no phase, reaches primary completion later than 26 of the 28 other live ones, and was the 81st registered.

Depression

8,582 studies on the registry are indexed under Depression; 1,723 are open to participants now.

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Open to participants now

23 of the 81 studies in Depression with a site in Pakistan are open now. Recruiting first, the newest first:

17 more — sign in →

All 23 open studies →

A study can be open while its sites in Pakistan have not opened yet or have stopped. Only those recruiting at a site in Pakistan →

Who these studies take

Of the 1,089 Depression studies recruiting now, 470 (43%) set no upper age limit and 519 (48%) stop at 75 or younger; 203 take children under 18; 311 take healthy volunteers.

This study: 18 Years to 65 Years · all sexes · no healthy volunteers.

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02

Study summary

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.

Read the detailed description

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 .

03

Conditions studied

  • Psychological Distress (Depression, Anxiety and Stress) Cancer

Keywords

  • Surah Ar Rahman, Psychological intervention , cancer patients, Randomized control trial
04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria:

  • 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

Exclusion Criteria:

    • 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)
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    intervention group

    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.

    Behavioral: supportive psychotherapy plus QURAN recitation9Surah Ar -Rahman

  • No intervention
    control group

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

Interventions

  • Behavioralsupportive psychotherapy plus QURAN recitation9Surah Ar -Rahman

    participants in experimental group will receive 12 week psychological intervention : weekly 30-45 min counseling based on supportive therapy plus daily listening to Surah Ar Rahman recitation ( Qari Abdul Basit , 20 min ) via audio player, participants will be provided audio and intructed to listen daily and maintain a log.

06

What researchers measure

Primary outcomes

  1. psychological distress (DASS-21)

    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

    Time frame: baseline and 12 weeks post intervention

Secondary outcomes

  1. Quality of Life -EORTC QLQ-C30

    Quality of life will be measured using European Organization for Research and treatment of Cancer Quality of life Questionnaire(EORTC-QLQ-C30) Version 3.0. it is 30-item questionnaire composed of 5 functional scales, 3 symptoms scales, a global health status scale and 6 single items. scores are transformed to 0-100 scale. higher score in functioning and global QoL indicates better QOL, higher score in symptoms indicates worse symptoms

    Time frame: Baseline and 12 week post-intervention

  2. Adult Hope scale(AHS)

    hope will be measured using Adult hope scale(Snyder et al.,1991). it is 12-items scale with 4 agency items , 4 pathways items, and 4 distractors. items are scored on an 8-point Likert scale from 1- definitely False to 8= definitely true. total score range is 8-64. excluding distractors. higher score indicates higher level of hope

    Time frame: baseline and 12 weeks post intervention

07

Study locations

1 site
  • Oncology department, IMPS, Noori & Shia International Hospital
    Islamabad, 44000, Pakistan
08

References and documents

Individual participant data

Plan to share: No — individual participants data(IPD) will not be shared due to ethical restrictions and to protect patient confidentiality as per institutional review board(IRB) policy. the study involved sensitive psychological data of cancer patients. De-identified summary data maybe available from principal investigator upon reasonable request after publication.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Sep 2026; primary completion for Nov 2027, 14 months later.

Of 3,471 non-industry interventional studies with no phase under Depression, half reached primary completion within 21 months of starting (the median), counting those still running; a quarter within 10 and three quarters within 41. This study's planned 14 months is below that.

Counting every sponsor, half of 3,569 studies reached it within 21 months; a quarter within 9 and three quarters within 41.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 16, 2026
First posted
Sep 22, 2026
StartEst.
Sep 15, 2026
Primary completionEst.
Nov 30, 2027
CompletionEst.
Dec 30, 2027
Last update
Sep 22, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07833982
Lead sponsor
Shaheed Zulfikar Ali Bhutto Institute of Science and Technology (SZABIST) University
Responsible party
Mobeen Mehmood (Principal investigator/PhD Scholar, Shaheed Zulfikar Ali Bhutto Institute of Science and Technology (SZABIST) University) — Principal investigator
First posted
Sep 22, 2026
Start date
Sep 15, 2026 (estimated)
Primary completion
Nov 30, 2027 (estimated)
Completion
Dec 30, 2027 (estimated)
Last update
Sep 22, 2026

Study contacts

mobeen mehmood, PhD
Contact
mobeen1770@gmail.com
03709191770

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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