Agitation rate. Anxiety disorder, unspecified
Conditions
Interventions
Intervention 1: Intervention group: In the intervention group, in addition to the routine care provided in the intensive care unit (for controlling anxiety and agitation, which includes the use of sed
Sponsors
Kerman University of Medical Sciences
Eligibility
Sex/Gender
All
Age
12 Years to 18 Years
Inclusion criteria
Inclusion criteria: Age 12 to 18 years GCS greater than or equal to 8 Admitted to intensive care units (ICU) Patient extubated at the time of study entry Hemodynamic stability No known history of hypersensitivity to lavender or other aromatic herbal compounds No history of chronic respiratory diseases No clinical signs or diagnosis of active pulmonary aspiration No primary or secondary immunodeficiency disorders Having a normal sense of smell Written informed consent from the patient’s parent or legal guardian
Exclusion criteria
Exclusion criteria: Patient intubation Transfer of the patient to other units Patient death Sudden and significant changes in hemodynamic status Occurrence of any side effects
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Aromatherapy. Timepoint: At the beginning and end of the intervention. Method of measurement: Charted information.;RASS (Richmond Agitation-Sedation Scale) SCORE. Timepoint: At 0, 6, 12, 18, and 24 hours after the start of the intervention. Method of measurement: RASS table. | — |
Secondary
| Measure | Time frame |
|---|---|
| BMI. Timepoint: At the beginning of the intervention. Method of measurement: File information.;Age. Timepoint: At the beginning of the intervention. Method of measurement: File information.;Gender. Timepoint: At the beginning of the intervention. Method of measurement: File information. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMehdi Ahmadinejad
Kerman University of Medical Sciences
Outcome results
None listed