Effect of structured auditory stimulation on the level of consciousness in patients' comatose with head trauma

Effect of structured auditory stimulation on the level of consciousness in patients' comatose in intensive care unit with head trauma admitted to hospital 5th Azar

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2012071810325N1

Enrollment

Registered

2012-08-06

Start date

2012-07-25

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

comatose patients with head trauma. Diseases of the nervous system-injury, poisoning and certain other consequences of external causes

Interventions

Intervention 1: Duration of intervention is 10 days and every day 3 times (in three shifts). Every auditory intervention is 15 minutes. A male nurse voice will be recorded and broadcasted for each pa

Prevention

Duration of intervention is 10 days and every day 3 times (in three shifts). Every auditory intervention is 15 minutes. A male nurse voice will be recorded and broadcasted for each patient as auditor

In the control group ther is no intervention and patients recieve standard care.

Eligibility

Sex/Gender

All

Age

15 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: the admitted comatose patients in ICU with head trauma in the Panje Azar hospital of Gorgan , Iran who have the following criteria will be selected: GCS=8, no have disorder or decrease in auditory function, no heart arrested for 4 minutes or upper, no having Precedence of : convulsion, brain damage, cardiovascular disease, fatty embolism, Rhinorrhea, otorrhea, fracture of basal skull, hemorrhage or surgery in temporal. exclusion criteria:Early death (before 10 days, early discharge, disagreement of the responsible of patient for continuing of intervention, and auditory disorder.

Exclusion criteria

Exclusion criteria:

Design outcomes

Secondary

Measure	Time frame
Blood pressure. Timepoint: 3 times in 24 hours. Method of measurement: blood pressure monitored based on mm Hg.;Pulse. Timepoint: 3 times in 24 hours. Method of measurement: pulse rate( counting) per minute.;Respiratory rate. Timepoint: 3 times in 24 hours. Method of measurement: counting respiratory rate per minute.;O2 saturation. Timepoint: 3 times in 24 hours. Method of measurement: the percent of hemoglobine o2 saturatin.	—

Measure

Time frame

Blood pressure. Timepoint: 3 times in 24 hours. Method of measurement: blood pressure monitored based on mm Hg.;Pulse. Timepoint: 3 times in 24 hours. Method of measurement: pulse rate( counting) per minute.;Respiratory rate. Timepoint: 3 times in 24 hours. Method of measurement: counting respiratory rate per minute.;O2 saturation. Timepoint: 3 times in 24 hours. Method of measurement: the percent of hemoglobine o2 saturatin.

—

Primary

Measure	Time frame
Level of consciousness. Timepoint: One time in each shift ( 3 times per 24 hours). Method of measurement: GCS criteria.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGholamreza Mahmoodi Shan

Golestan University of Medical Sciences

Mahmoudi@goums.ac.ir; Mahmoodigh@yahoo.com+98 17 1442 6900

Outcome results

None listed

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