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Effect of reciting the word Allah on the pain and anxiety after coronary artery bypass graft surgery

Effect of reciting the word Allah on the pain and anxiety after coronary artery bypass graft surgeryo in paients who refferred to ICU ward of Busheher Fatemah Zahra (s) Hospital in 2013.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013080314251N1
Enrollment
80
Registered
2014-02-14
Start date
2013-08-11
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Condition 1: pain after CABG operation. Condition 2: anxiety after CABG operation. Chest pain, unspecified Acute stress reaction

Interventions

Intervention 1: at least 4 hours afterrecieving analgesic after operation, we aske patients to recite Hazrate Zahra Praises that word “Allah” becomes repeated 100 times.Pain severity,anxiety, vital
Treatment - Other
at least 4 hours afterrecieving analgesic after operation, we aske patients to recite Hazrate Zahra Praises that word “Allah” becomes repeated 100 times.Pain severity,anxiety, vital signs, and the a
In control group no intervent will do.Pain severity,anxiety, vital signs, and the amount of medication used will assesse before and 24, 48 and 72 hours after surgery

Sponsors

Ahvaz Jundishapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusioncriteria: more than 25 years old? be Muslium? using Saphen vein for tranplantation? be able to understand study details? eager to participate in the study? underwent to CABG operation for the first time? lack of pacemaker? having elective CABG operation? be connected to the crdiopulmunary bypass pump less than 4 hours. exclusion criteria : lack of alertness? needs to intraaurta pump? be intubated more than 24 hours? bleeding more than 200 cc per hour from chest tube? doing valve repairment or replacment operations with CABG? having sever articulation disorder? having sever visual disorders? sufferring from chronic pain? being addicted to analgesic or alchohol .

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: before and 24-48 and 72 hours after intervantion. Method of measurement: VAS scale.;Anxiety. Timepoint: before and 24-48 and 72 hours after intervantion. Method of measurement: hospital anxiety questioner.

Secondary

MeasureTime frame
Percentage of saturated oxyhemoglobin. Timepoint: before and 24-48 and 72 hours after intervantion. Method of measurement: by questioner.;Reception of extra Analgesics Drugs rate. Timepoint: before and 24-48 and 72 hours after intervantion. Method of measurement: by cheklist.;Satisfaction. Timepoint: after intervantion. Method of measurement: by cheklist.;Vital signs. Timepoint: before and 24-48 and 72 hours after intervantion. Method of measurement: by blood presure cuff- termometer and watch.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMorteza Nasiri

Ahvaz Jundishapor University of Medical Sciences

mortezanasiri.or87@yahoo.comnasiri.m@ajums.ac.ir+98 77 2622 5292

Outcome results

None listed

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