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Auditory stimulation in comatose patients

Auditory stimulation by family voices and recitation of prayers on consciousness level and hemodynamic changes of comatose patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014081418794N1
Enrollment
51
Registered
2015-02-23
Start date
2013-06-24
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

Traumatic Brain Injury. Intracranial injury

Interventions

Intervention 1: Patient familiar voice was recorded with mp3 by Mark Marshall. This sound contains was introduction to a patient, slight accident occurred and reassuring messages. Sounds were delivere
Patient familiar voice was recorded with mp3 by Mark Marshall. This sound contains was introduction to a patient, slight accident occurred and reassuring messages. Sounds were delivered through headph
The sound of the call to prayer of the muezzin's voice was born. The call duration is approximately 4 minutes that 14 days this sound like a familiar voice, twice daily at noon and evening prayer for
The control group did not receive any intervention by the researcher.It's just routine hearing voices.In this group, twice daily for 14 days, Level of consciousness and hemodynamics were recorded.

Sponsors

Medical Sciences Vice Chancellor for Research, Zanjan University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 68 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for this study included: Comatose traumatic patients; Muslim patients; Ages range from 68-14 years; Levels of consciousness 8 and less than 8; No fracture and surgery for temporal lobe; The lack of swelling of both eyelids; Absence of severe mental illness; Absence of Fracture four limbs; Family consent for participation in the study; The absence of hearing loss. Exclusion criteria included: patient died before day 14 in both groups; Swelling of both eyelids; Changes in the patient's condition so that the possibility of intervention , such as sending a patient away to another hospital, cardiac arrest.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Level of Consciousness. Timepoint: pre and post intervention. Method of measurement: GCS Scale.;Hemodynamic Status. Timepoint: pre and post intervention. Method of measurement: Monitoring sistem and Termometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Mogadam

Zanjan University of Medical Science

Fateme.mogadam@gmail.com; payami@zums.ac.ir+98 24 3575 3185

Outcome results

None listed

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