The effectiveness of tactile stimulation on unconscious patients
- Conditions
- comatose patient.Coma, unspecifiedB19.10
- Registration Number
- IRCT20110912007529N22
- Lead Sponsor
- Shahed University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 90
Age range 18 to 60 years old
The level of consciousness based on Glasgow coma scale is less than 12
The Richmond criteria in the range of 3- to 3+
Existence of pain in patients by CPOT criteria
Existence of normal brain CT
Hospitalization in ICU for the first time
The lack of history of mental illness
The lack of addiction
The lack of sensory-motor dysfunction in the extremities
The lack of skin problems
The lack of diseases such as diabetes
Concurrent participation in similar care plans such as massage
Use of receive neuromuscular blockers
Severe disorders levels of consciousness
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method evel of consciousness. Timepoint: Before and after intervention, twice a day, during three days. Method of measurement: The GCS and FOUR scores.;Intensity of pain. Timepoint: Before and after intervention, twice a day, during three days. Method of measurement: Critical Care Pain Observation Tool (CPOT).
- Secondary Outcome Measures
Name Time Method Blood Pressure. Timepoint: Before and after intervention, twice a day, during three days. Method of measurement: The monitor used in Intensive Care Unit.;Respiratory Rate. Timepoint: Before and after intervention, twice a day, during three days. Method of measurement: The monitor used in Intensive Care Unit.;Heart Rate. Timepoint: Before and after intervention, twice a day, during three days. Method of measurement: The monitor used in Intensive Care Unit.;Oxygen Saturation. Timepoint: Before and after intervention, twice a day, during three days. Method of measurement: Pulse Oximeter.