MedPath

The effectiveness of tactile stimulation on unconscious patients

Not Applicable
Conditions
comatose patient.
Coma, unspecified
B19.10
Registration Number
IRCT20110912007529N22
Lead Sponsor
Shahed University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
90
Inclusion Criteria

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

Exclusion Criteria

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
NameTimeMethod
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
NameTimeMethod
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.
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