Stroke. Transient cerebral ischaemic attacks and related syndromes,Vascular syndromes of brain in cerebrovascular diseases
Conditions
Interventions
Intervention 1: intervention group: Implication of sensory stimulation program include of auditory, visual, olfactory, gustatory, tactile and kinesthetic stimulation. At first select the stimulus acc
intervention group: Implication of sensory stimulation program include of auditory, visual, olfactory, gustatory, tactile and kinesthetic stimulation. At first select the stimulus according to the pa
In the control group will not be performed any intervention except routine care
Sponsors
Vice Chancellor for Research and Technology, Mashhad University of Medical Sciences
Eligibility
Sex/Gender
All
Age
35 Years to 75 Years
Inclusion criteria
Inclusion criteria: Inclusion Criteria: age between 35 to 75 years; duration of coma more than 72 hours and less than 14 days; GCS between 6 and 12; the availability of one of the patient's family who is over 18 years; family consent of the patient to participate in the study; Iranian citizenship and fluent in Persian; lack of vision problems and blindness; no hearing problems; the absence of psychotic mental illness; the lack of skin problems; the lack of sedative and narcotic Exclusion Criteria: metabolic disorders; drug addiction; get sedatives and drugs during the study; the prohibition in mobility organs; sensory-motor disorder in four limbs; patients who have suffered from a stroke in the areas of visual and auditory nerves; identification of vision problems; hearing problems; skin diseases and psychological problems during the study; sudden hemodynamic disorder that can cause critical situations for patients; died before the fourteenth days
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Coma recovery. Timepoint: before and after of intervention for 14 consecutive days. Method of measurement: CRS-R.;Sensory function. Timepoint: before and after of intervention for 14 consecutive days. Method of measurement: SMART.;Cognitive function. Timepoint: before and after of intervention for 14 consecutive days. Method of measurement: RLA.;The severiety of stroke. Timepoint: before intervention at first day, seventh and fourtheen days after intervention. Method of measurement: NIHSS. | — |
Secondary
| Measure | Time frame |
|---|---|
| HemodynamicCriteria:PR,RR,BP,SPo2. Timepoint: before and after intervention for 14 consecutive days. Method of measurement: Cardiopulmonary monitoring and Sphygmomanometer. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactKhadijeh Sargolzaei
Mashhad University of Medical Sciences, School of Nursing and Midwifary
Outcome results
None listed