Patients admitted to the intensive care unit.
Conditions
Interventions
Intervention 1: Intervention group one:The familiar voice group receives recorded voice messages from family members (the person who has the most contact with the patient) for 3 consecutive days. Inte
Sponsors
Arak University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: • Consent to participate in the study by the patient's legal guardian. Age 18 to 65 years The level of consciousness of the patients is between 5 and 8 according to the Glasgow Coma Scale and they are also intubated and under a ventilator No hearing diseases or any dressings in the ear area No receipt of sedatives or tranquilizers 24 hours before entering the study
Exclusion criteria
Exclusion criteria: • Death of the patient Discharge of the patient from the intensive care unit• Receiving antihypertensive or blood pressure-increasing drugs Occurrence of events that change the hemodynamics of the patients, such as shock and cardiac arrest... Unwillingness to continue the study by the legal guardian
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Heart rate. Timepoint: 5 minutes before the intervention and 5 minutes after the intervention. Method of measurement: By means of the monitor device available in the department (SAZGAN VECTRA model). | — |
Secondary
| Measure | Time frame |
|---|---|
| Systolic blood pressure. Timepoint: 5 minutes before the intervention and 5 minutes after the intervention. Method of measurement: By means of the monitor device available in the department (SAZGAN VECTRA model).;Diastolic blood pressure. Timepoint: 5 minutes before the intervention and 5 minutes after the intervention. Method of measurement: By means of the monitor device available in the department (SAZGAN VECTRA model).;Mean arterial blood pressure. Timepoint: 5 minutes before the intervention and 5 minutes after the intervention. Method of measurement: By means of the monitor device available in the department (SAZGAN VECTRA model).;Respiratory rate. Timepoint: 5 minutes before the intervention and 5 minutes after the intervention. Method of measurement: By means of the monitor device available in the department (SAZGAN VECTRA model).;Arterial blood oxygen saturation. Timepoint: 5 minutes before the intervention and 5 minutes after the intervention. Method of measurement: By means of the monitor device available in the department (SAZGAN VECTRA model). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMajid Koushki
Arak University of Medical Sciences
Outcome results
None listed