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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: IRCT
Last refreshed on: 22 February 2018
Main ID:  IRCT2017071135010N1
Date of registration: 2017-08-16
Prospective Registration: No
Primary sponsor: arshad
Public title: Virtual reality jn stroke
Scientific title: effect of virtual reality on mobility in stroke in comparison with task oriented training P: Stroke I: Virtual reality training O= mobility C- task oriented training
Date of first enrolment: 2017-07-31
Target sample size: 60
Recruitment status: Recruiting
URL:  http://en.irct.ir/trial/26591
Study type:  interventional
Study design:  Randomization: Randomized, Blinding: Single blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Other design features: two groups, homogeneous , age 40-70 years.  
Phase:  N/A
Countries of recruitment
Pakistan
Contacts
Name: arshad   
Address:  Railway hospital Rawalpindi Pakistan
Telephone: 0092515481826
Email: physiomalik1@gmail.com
Affiliation:  Riphah international university
Name: arshad   
Address:  railway hospital rawalpindi Pakistan
Telephone: 0092515481826
Email: physiomalik1@gmail.com
Affiliation:  riphah international university
Key inclusion & exclusion criteria
Inclusion criteria: inclusion criteria: Stroke after 03 month of onset
able to stand for 10 seconds; exclusion criteria: cognitive impairment fracture

Exclusion criteria:

Age minimum: 40 years
Age maximum: 70 years
Gender: Both
Health Condition(s) or Problem(s) studied
Stroke.
Vascular syndromes of brain in cerebrovascular diseases
Vascular syndromes of brain in cerebrovascular diseases
Intervention(s)
Intervention 1: Intervention:Virtual reality additional protocol. 10 to 20 minutes. Intervention 2: Control: Task oriented training.
Rehabilitation
Control: Task oriented training
Intervention:Virtual reality additional protocol. 10 to 20 minutes
Primary Outcome(s)
Berg balance scale. Timepoint: 08 weeks. Method of measurement: subjective scoring.
Fugl-meyer performance. Timepoint: 08 weeks. Method of measurement: subjective.
Secondary Outcome(s)
Stroke specific quality of life. Timepoint: 08 weeks. Method of measurement: subjective.
Timed up and go test. Timepoint: 08 weeks. Method of measurement: timer.
Secondary ID(s)
Source(s) of Monetary Support
arshad
Secondary Sponsor(s)
Ethics review
Status: Approved
Approval date:
Contact:
Riphah scientific and ethical committee
Results
Results available:
Date Posted:
Date Completed:
URL:
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