Sensory stimulation in Stroke comatose patients

Phase 2

Conditions: Stroke.
Transient cerebral ischaemic attacks and related syndromes,Vascular syndromes of brain in cerebrovascular diseases
G45, G46

Registration Number: IRCT2016120831299N1

Lead Sponsor: Vice Chancellor for Research and Technology, Mashhad University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Complete

Sex: All

Target Recruitment: 80

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

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
HemodynamicCriteria:PR,RR,BP,SPo2. Timepoint: before and after intervention for 14 consecutive days. Method of measurement: Cardiopulmonary monitoring and Sphygmomanometer.