- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06326541
The Effect of Listening to the Holy Quran on Vital Signs in Coma Patients
March 17, 2024 updated by: Serafettin Okutan, Bitlis Eren University
The Effect of Listening to the Holy Quran on Life Findings in Coma Patients Hospitalized in Surgical Intensive Care Unit
The aim of this study is to examine the effect of the Holy Quran listened to to coma patients on their vital signs.
Does listening to the Holy Quran have a positive effect on the life values of coma patients?
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
This study aims to examine the effect of listening to the Holy Quran on vital signs (fever, pulse, respiration, systolic-diastolic blood pressure, saturation) in surgical intensive care unit patients.
The unique value of this study, unlike other studies, is to examine the positive changes in patients' vital signs by listening to the Holy Quran (Surah Rahman) instead of classical music.
Study Type
Interventional
Enrollment (Actual)
72
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Bitlis, Turkey, 13100
- Bitlis Eren University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Being over 18 years of age
- Being a surgical intensive care patient
- Having a Glasgow coma score of 8 points or less
Exclusion Criteria:
- The patient must be under 18 years of age
- Have a Glaskow coma score above 8 points
- Be out of coma during the time the research continues
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: music therapy
|
Listening to the Holy Quran.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
systolic blood pressure- (mmHg)
Time Frame: 30 minutes
|
Vital Signs Values of Patients Before and After Application
|
30 minutes
|
diastolic blood pressure- (mmHg)
Time Frame: 30 minutes
|
Vital Signs Values of Patients Before and After Application
|
30 minutes
|
pulse (number of beats/min)
Time Frame: 30 minutes
|
Vital Signs Values of Patients Before and After Application
|
30 minutes
|
body temperature (degrees Celsius)
Time Frame: 30 minutes
|
Vital Signs Values of Patients Before and After Application
|
30 minutes
|
saturation (%-oxygen saturation)
Time Frame: 30 minutes
|
Vital Signs Values of Patients Before and After Application
|
30 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Şerafettin OKUTAN, Dr., Bitlis Eren University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 5, 2023
Primary Completion (Actual)
December 10, 2023
Study Completion (Actual)
December 30, 2023
Study Registration Dates
First Submitted
March 6, 2024
First Submitted That Met QC Criteria
March 17, 2024
First Posted (Actual)
March 22, 2024
Study Record Updates
Last Update Posted (Actual)
March 22, 2024
Last Update Submitted That Met QC Criteria
March 17, 2024
Last Verified
March 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- okutan
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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