Investigation the therapeutic effect of Holy Quran voices on anxiety in cardiac care unit patients

Investigation the therapeutic effect of Holy Quran voices on anxiety in cardiac care unit patients in Hazrat Zahra hospital at Khomein city.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20240609062052N2

Enrollment

Registered

2024-06-27

Start date

2024-06-26

Completion date

Unknown

Last updated

2025-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: Angina pectoris. Condition 2: Essential (primary) hypertension. Condition 3: Atherosclerosis. Condition 4: myocardial infarction. Condition 5: Aortic aneurysm and dissection. Angina pectoris Essential (primary) hypertension Atherosclerosis ST elevation (STEMI) and non-ST elevation (NSTEMI) myocardial infarction Aortic aneurysm and dissection

Interventions

Intervention 1: Intervention group: the sound of the Quran in this study, which is a clinical trial type

68 patients admitted to the CCU department of Imam Khomeini Hospital (RA) in Khomein city who meet the inclusion criteria

34 people are randomly assigned to the Qur'an group. The data collection tool is a two-part questionnaire, the first part of which is related to demographic information and the second part is related

Then, for 15 minutes, they listen to Surah Hamad and verses 1 to 20 of Surah Yusuf in the voice of Professor Abdul Basit. The selection of this surah is based on the previous studies conducted in the

68 patients admitted to the CCU department of Imam Khomeini Hospital (RA) in Khomein city, who meet the criteria for entering the study

34 people are randomly assigned to the control group. The data collection tool is a two-part questionnaire, the first part of which is related to demographic information and the second part is related

Then no intervention is done for the control group and they complete the Spielberger test again like the intervention group. Then the results of control and intervention groups will be compare

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Having informed consent Being aware of time, place and people Having a healthy sense of hearing

Exclusion criteria

Exclusion criteria: History of drug and alcohol addiction History of mental illnesses History of new crisis such as death of first degree relatives, divorce of self or parents in the last 6 months The patient's refusal to continue participating in the study Critical condition of the patient

Design outcomes

Primary

Measure	Time frame
Anxiety score in Spielberger questionnaire. Timepoint: Before and after the intervention. Method of measurement: Anxiety:Spielberger questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactPouya Zeidy

Khomein Faculty of Medical Sciences

zeidypouya@gmail.com+98 86 4622 3435

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026