The effect of Organized auditory stimulation with familiar voices on the level of consciousness and hemodynamic status of coma patients

The effect of Organized auditory stimulation with familiar voices on the level of consciousness and hemodynamic status of coma patients hospitalized in intensive care unit

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2014051517693N1

Enrollment

Registered

2014-08-14

Start date

2014-06-22

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

Head Trauma,Brain injury,Intracranial injury. Multiple injuries of head,Other specified injuries of head,Intracranial injury

Interventions

Intervention 1: Organized auditory stimuli in the intervention group for 3 days,Once daily (evening shift) for 10 minutes With the voice of a person of interest to the patient becomes sick auditory st

Prevention

Organized auditory stimuli in the intervention group for 3 days,Once daily (evening shift) for 10 minutes With the voice of a person of interest to the patient becomes sick auditory stimulation.The co

The control group did not receive intervention

Eligibility

Sex/Gender

All

Age

16 Years to 139 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: the admitted comatose patients in ICU with head trauma in the PourSina hospital of Rasht , Iran who have the following criteria will be selected: GCS=8, Artificial airway (endotracheal tube - the mouth or nose - or tracheostomy), 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 or discharge (before 3 days),Hemodynamic changes during intervention(A sudden increase or decrease in systolic and diastolic pressures over mmhg 20 compared to baseline,A sudden increase or decrease in heart rate over 20 beats to the base,Increased respiratory rate more than 25 and decreased more than 8 times per minute compared to the baseline)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Level of consciousness. Timepoint: Once a day for three consecutive days. Method of measurement: GCS criteria.	—

Secondary

Measure	Time frame
Blood pressure. Timepoint: Once a day for three consecutive days. Method of measurement: blood pressure monitoring based on mm Hg.;Pulse. Timepoint: Once a day for three consecutive days. Method of measurement: pulse rate( counting) per minute by monitoring.;Respiratory rate. Timepoint: Once a day for three consecutive days. Method of measurement: respiratory rate counting per minute.;Body temperature. Timepoint: Once a day for three consecutive days. Method of measurement: With axillary thermometer based on C.	—

Measure

Time frame

Blood pressure. Timepoint: Once a day for three consecutive days. Method of measurement: blood pressure monitoring based on mm Hg.;Pulse. Timepoint: Once a day for three consecutive days. Method of measurement: pulse rate( counting) per minute by monitoring.;Respiratory rate. Timepoint: Once a day for three consecutive days. Method of measurement: respiratory rate counting per minute.;Body temperature. Timepoint: Once a day for three consecutive days. Method of measurement: With axillary thermometer based on C.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Kazem Mohammadi

Guilan University of Medical Sciences

Mohammadkm64@Gmail.com+98 13 1226 5049

Outcome results

None listed

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