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PNF and Myofascial Release in patients with CVA

Not Applicable
Conditions
Patients with CVA.
Registration Number
IRCT20200209046422N1
Lead Sponsor
Gorgan Red Crescent Rehabilitation Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
45
Inclusion Criteria

Patients with CVA diagnosed by a neurologist
Age range 45-60 years
Spasticity level +1 or 2 according to the Ashworth scale
No active phase of the disease
Having a stroke once
4 to 8 months have passed since receiving the last rehabilitation services for stroke patients
Absence of spinal cord lesions
Lack of regular sports activity
Failure to receive PNF technique from 6 months ago
Personal and informed consent to participate in the study

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Wrist function. Timepoint: Measurement of wrist function before the start of the research and re-measurement after 12 intervention sessions. Method of measurement: Fugl meyer assessment.;Range of motion of wrist. Timepoint: Measurement of range of motion of the wrist before the beginning of the research and its re-measurement after 12 intervention sessions. Method of measurement: Measure with a goniometer.;Quality of Life. Timepoint: Measuring the quality of life before the start of the research and measuring it again after 12 intervention sessions. Method of measurement: Using the World Health Organization Quality of Life questionnaire.
Secondary Outcome Measures
NameTimeMethod
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