Condition 1: physiological parameters. Condition 2: delirium. Condition 3: pain. R00.0/R00.1/R03.0/R03.1/R06.4/R06.8 F05.9/F05.8 R52.0/R52.2
Conditions
Interventions
Intervention 1: Control group: No action. Intervention 2: Intervention group 1: Foot Swedish massage is given by nurse for six days, once a day, and every leg for 5 minutes. Intervention 3: Interventi
Treatment - Other
Control group: No action
Intervention group 1: Foot Swedish massage is given by nurse for six days, once a day, and every leg for 5 minutes.
Intervention group 2: Foot Swedish massage is given by patient’s family for six days, once a day, and every leg for 5 minutes.
Sponsors
investigator
Eligibility
Sex/Gender
All
Age
15 Years to 50 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Patients with tracheal tube or tracheostomy? (GCS) (9-11) in patients with tracheal tube and tracheostomy , lack of continuous infusion of sedative drugs such as midazolam and propofol, lack of continuous infusion of narcotics such as fentanyl, no history of mental disorders such as Psychosis and mental retardation, knowledge of Farsi, able to co-operate in the field of vision and hearing, ages 50-15, Absence of Withdrawal syndrome, not having foot vascular disorders such as DVT with doctor's diagnosis, no fractures in the lower limbs, lack of Skin disease, ulcers and foot infections. Exclusion criteria: loss of consciousness less than 9, extubation, death of the patient, discharge, skin diseases such as ulcers and infections of feet, Suffering from vascular disorders such as DVT
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Delirium. Timepoint: before of the intervention, 30 minutes after of the intervention (6 day) and one week after of the intervention (day 13). Method of measurement: CAMICU tool.;Pain. Timepoint: before of the intervention, 30 minutes after of the intervention (6 day) and one week after of the intervention (day 13). Method of measurement: Behavioral Scale of Pain (BPS).;Physiological parameters. Timepoint: before of the intervention, 30 minutes after of the intervention (6 day) and one week after of the intervention (day 13). Method of measurement: Using of monitored device. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMansour Arab
Razi Nursing and Midwifery School
Outcome results
None listed