Condition 1: physiological parameters. Condition 2: sleep quality.
Conditions
Interventions
Intervention 1: Intervention group: In the intervention group, hands and feet will be massaged with mint oil(Noorhan Company) mixed with sweet almond(Noorhan Company) oil for 20 minutes. The intervent
Sponsors
Kerman University of Medical Sciences
Eligibility
Sex/Gender
All
Age
15 Years to 65 Years
Inclusion criteria
Inclusion criteria: Level of consciousness according to the Glasgow Coma scale 12-15 Less than six months and more than 48 hours of hospitalization Patient age in the range of 15 to 65 years
Exclusion criteria
Exclusion criteria: A sudden drop in the level of consciousness Transfer to another hospital Discharge before the fourth day Death of patients in both intervention and control groups during the study At the same time, the patient participates in similar care programs such as massage therapy History of chronic disease (diabetes, cardiovascular disease, epilepsy and kidney disease) and endocrine disorders (Cushing's syndrome and hypo / hyperthyroidism) A history of sensorineural disorders, coma, or previous head injury Evidence of increased intracranial pressure (ICP) and symptoms of fat embolism Wounds, inflammation, infection, skin diseases and fractures in the massage areas
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Heart rate. Timepoint: Heart rate will be measured before intervention, 5 minutes after intervention, one hour after intervention, 2 hours after intervention, 3 hours after intervention, 4 hours after intervention and for three consecutive days. Method of measurement: Monitoring device. | — |
Secondary
| Measure | Time frame |
|---|---|
| Systolic blood pressure. Timepoint: Systolic blood pressure will be measured before intervention, 5 minutes after intervention, one hour after intervention, 2 hours after intervention, 3 hours after intervention, 4 hours after intervention and for three consecutive days. Method of measurement: Monitoring device.;Diastolic blood pressure. Timepoint: diastolic blood pressure will be measured before intervention, 5 minutes after intervention, one hour after intervention, 2 hours after intervention, 3 hours after intervention, 4 hours after intervention and for three consecutive days. Method of measurement: Monitoring device.;Respiratory rate. Timepoint: Breathing will be measured before intervention, 5 minutes after intervention, one hour after intervention, 2 hours after intervention, 3 hours after intervention, 4 hours after intervention and for three consecutive days. Method of measurement: Observed by the researcher.;Arterial blood oxygen saturation. Timepoint: Arterial blood oxygen saturation will be measured before intervention, 5 minutes after intervention, one hour after intervention, 2 hours after intervention, 3 hours after intervention, 4 hours after intervention and for three consecutive days. Method of measurement: Monitoring device.;Sleep quality. Timepoint: Sleep quality will be measured before the intervention and the fourth day. Method of measurement: Richard Campbell sleep questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactBatool Tirgari
Kerman University of Medical Sciences
Outcome results
None listed