Coma. Unconsciousness NOS
Conditions
Interventions
Intervention 1: Control group: In this group, headphones are worn by patients (with playing no sound) without any other stimuli for 10 minutes for a week. Intervention 2: Intervention group: In this g
Control group: In this group, headphones are worn by patients (with playing no sound) without any other stimuli for 10 minutes for a week.
Intervention group: In this group, sound stimuli pleasant for patients are played for 10 minutes for one week with headphones without any other stimuli.
Sponsors
Student Research Committee, Vice Chancellor for research and technology of Kurdistan University of M
Eligibility
Sex/Gender
All
Age
15 Years to 75 Years
Inclusion criteria
Inclusion criteria: Alertness level equal to and less than 8 according to Glasgow Patients aged 15-75 years 24Hours after vital signs are sustained in the intensive care unit Not taking antidepressants or affecting restlessness and tranquilizers and Opiums Absence of mental disorders No previous brain damage No impairment or hearing loss Lack of cerebrospinal fluid or blood from the ears and nose Non-fracture, bleeding and temporal and temporal area surgery No addiction Not getting cancer Lack of fracture in four limbs or quadriplegic No significant changes in intracranial pressure
Exclusion criteria
Exclusion criteria: Discharge or death of the patient before day 6 Cancellation of the patient's continuation of the study Severe changes in vital signs Severe changes in mental status Severe changes in intracranial pressure Destruction of brain stem reflex during research
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hemodynamic parameters. Timepoint: Before, immediately and ten minutes after the intervention. Method of measurement: Systole and diastolic blood pressure with mercuric pressure gauge, moderate blood pressure with the corresponding formula, pulse pressure by decreasing systole pressure from diastol, oxygen saturation with plusoxymmeters.;Agitation. Timepoint: Before, immediately and ten minutes after the intervention. Method of measurement: Using Richmond Agitation-Sedation Scale (RASS).;Level of consciousness. Timepoint: Before, immediately and ten minutes after the intervention. Method of measurement: Using the Glasgow coma scale (GCS). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFarzad Rahimi
Vice Chancellor for research and technology of Kurdistan University of Medical Sciences
Outcome results
None listed