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Tavvasol Praying for anxiety

Assessment the effect of Tavvasol Praying on anxiety and physiologic parameters in patients with myocardial infarction admitted to Coronary Care Unit

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017071818550N5
Enrollment
80
Registered
2017-08-15
Start date
2017-08-23
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

Anxiety. Anxiety disorder, unspecified

Interventions

Intervention 1: Intervention1: Playing the audio file of the Tavvasol Praying via headphones, at 6 hour after admission to CCU and 24 hours after first time playing. Intervention 2: Intervention 2: Co
Intervention1: Playing the audio file of the Tavvasol Praying via headphones, at 6 hour after admission to CCU and 24 hours after first time playing.
Intervention 2: Control group recieve routine care.

Sponsors

Vice chancellor for research and technology, Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age over 40; Muslim and Shiite; lack of history of anxiety and psychiatric disorders; lack of hearing problems; hospitalization for paradise in cardiac care unit Exclusion criteria: Taking a sedative during the study; under the cardio-pulmonary resuscitation of the CCU during the study and heart dysrhythmias during the study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: In 4 times: 6 hours after hospitalization in CCU, immediately after intervention for first time and 24 hours after first time intervention and immediately after intervention for second time. Method of measurement: Hospital Anxiety questionnaire.

Secondary

MeasureTime frame
Blood Pressure. Timepoint: In 4 times: 6 hours after hospitalization in CCU, immediately after intervention for first time and 24 hours after first time intervention and immediately after intervention for second time. Method of measurement: Digital Spyghmomanometer.;Heart Rate. Timepoint: In 4 times: 6 hours after hospitalization in CCU, immediately after intervention for first time and 24 hours after first time intervention and immediately after intervention for second time. Method of measurement: Digital manometer.;O2 Saturation. Timepoint: In 4 times: 6 hours after hospitalization in CCU, immediately after intervention for first time and 24 hours after first time intervention and immediately after intervention for second time. Method of measurement: Digital Pulse Oximeter.;Body Temperature. Timepoint: In 4 times: 6 hours after hospitalization in CCU, immediately after intervention for first time and 24 hours after first time intervention and immediately after intervention for second time. Method of measurement: Digital Tympanic Membrane termometer.;Respiration Rate. Timepoint: In 4 times: 6 hours after hospitalization in CCU, immediately after intervention for first time and 24 hours after first time intervention and immediately after intervention for second time. Method of measurement: Digital manometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNayyereh Raiesdana

Semnan University of Medical Sciences

nr_dana@semums.ac.ir; nr_dana@yahoo.com+98 23 3365 4190

Outcome results

None listed

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