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Comparing The effect of family members' voice and nurse' voice on restlessness, anxiety, delirium and success in weaning of ventilator in patients admitted to Intensive Care Units

Comparing The effect of family members' voice and nurse' voice on restlessness, anxiety, delirium and success in weaning of ventilator in patients admitted to Intensive Care Units

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201014049029N1
Enrollment
90
Registered
2020-11-18
Start date
2020-08-22
Completion date
Unknown
Last updated
2020-11-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Head trauma. Crushing injury of other parts of head, sequela

Interventions

Intervention 1: Intervention group: the voice of a family member is recorded and played to patients through a headset. This intervention is performed twice a day for six days for patients. In the inte

Sponsors

Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.The age of patients should be between 18-65 years 2.The level of consciousness according to the Glasgow coma criterion due to trauma should be 11-8 3.The patient has been admitted to the ward with a diagnosis of concussion. Traumatic brain injury includes subdural, epidural, intracerebral, ventricular, and subarachnoid hemorrhages. 4.Sedation should be in the range of +2 to 2- according to Richmond criteria 5.48 hours have elapsed since hospitalization 6.Patients should have at least one healthy hearing position according to the physician or ENT consultation 7.Have no previous history of hearing loss according to family statements 8.Do not have a bandage on the ear 9.No history of depression and other mental disorders 10.Family availability and collaboration to record audio 11.Do not use alcohol and drugs with high dependence before the accident according to family statements

Exclusion criteria

Exclusion criteria: 1.Dissatisfaction of the patient's companions to continue participating in the study 2.A history of hearing, vision, aphasia and limb movement disorders 3.Patients with vegetative status as determined by physician 4.Patients with severe previous head injury 5.Sudden loss of consciousness more than 3 points according to the Glasgow Coma Criterion during the intervention 6.Simultaneous participation of the patient in similar care programs such as massage therapy and the use of relaxation techniques and ...

Design outcomes

Primary

MeasureTime frame
Restlessness was assessed by the Richmond Restlessness Checklist. The Richmond tool consists of 10 levels, four of which are for restlessness, one for calm and alert, and five for relaxation. Timepoint: Before and after the intervention. Method of measurement: Richmond Restlessness Checklist.;Delirium is assessed with the Neecham Delirium instrument and this questionnaire has a total of 30 points. Based on the overall score obtained by the patient, it is divided into 4 categories; A healthy person with a score of 27-30, prone to confusion with a score of 25-26, mild delirium with a score of 20-24, moderate to severe delirium with a score of 0-19. Timepoint: Before and after the intervention. Method of measurement: Neecham Delirium questionnaire.;Anxiety was assessed with the Facial Anxiety Scale. It has a range from 1 to 5, the lowest of which is related to the normal state of the facial state and the highest of which is the number 5 related to the maximum state of anxiety. Timepoint: Before and after the intervention. Method of measurement: Facial Anxiety Scale.;Weaning success was assessed with the Burn weaning Success Tool. The total score is 26 and after receiving a score of 17 or higher, the separation process begins. Timepoint: Before and after the intervention. Method of measurement: Burn weaning Success Tool.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFariba Abdollahi

Qazvin University of Medical Sciences

FaribaAbdollahi93@gmail.com+98 28 3333 7006

Outcome results

None listed

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