Physiological indicators and pain caused by changes in the condition of patients with cerebrovascular accidents. _Sequelae of stroke, not specified as haemorrhage or infarction
Conditions
Interventions
Intervention 1: The first Intervention group: Aromatherapy with lavender oil is an intervention that aims to reduce pain and improve physiological indicators in the present study. This intervention wi
Sponsors
Artesh University of Medical Sciences
Eligibility
Sex/Gender
All
Age
65 Years to No maximum
Inclusion criteria
Inclusion criteria: 1_ Patients with a cerebrovascular accident confirmed by a physician 2_ Age over 65 years 3_ Patients without a history of asthma and chronic respiratory disease 4_ Patients without a history of allergy to lavender based on the statement of the patient or the patient's companion 5_ Patients without a history of olfactory disorders 6_ Patients without a history of psoriasis 7_ Absence of drug addiction 8_ Patients without intubation in the trachea 9_ Healthy skin of the hands 10_ Being hospitalized in the intensive care unit for at least 24 hours 11_ Patient not using painkillers, narcotics and sedatives 6-8 hours before, while and after the intervention 12- Not having an angioket at the massage site 13- Patients without receiving drugs that increase or decrease blood pressure such as: epinephrine, dopamine, dobutamine, TNG, etc. 14- Patients without receiving anticonvulsant drugs such as: Gabapentin
Exclusion criteria
Exclusion criteria: 2_The patient's sensitivity to lavender during the intervention 3_Irritation and skin damage in the hands area during the study 4_Instability and sudden changes in the patient's condition 5_The need to intubate the patient during the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain score in Critical care Pain Observation Tool. Timepoint: Before the intervention and immediately after the change of the patient's condition for 3 consecutive days. Method of measurement: Critical care Pain Observation Tool.;Systolic Blood Pressure. Timepoint: Before the intervention and immediately after the change of the patient's condition for 3 consecutive days. Method of measurement: The monitor is available in the manufacturing department of Sa Iran company.;Diastolic Blood Pressure. Timepoint: Before the intervention and immediately after the change of the patient's condition for 3 consecutive days. Method of measurement: The monitor is available in the manufacturing department of Sa Iran company.;Respiratory Rate. Timepoint: Before the intervention and immediately after the change of the patient's condition for 3 consecutive days. Method of measurement: The monitor is available in the manufacturing department of Sa Iran company.;Pals Rate. Timepoint: Before the intervention and immediately after the change of the patient's condition for 3 consecutive days. Method of measurement: The monitor is available in the manufacturing department of Sa Iran company. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMahsa Karami
Artesh University of Medical Sciences
Outcome results
None listed