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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05898971
Other study ID # BMC
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date April 12, 2023
Est. completion date October 11, 2023

Study information

Verified date September 2023
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

robotic glove training could be a useful aid for these patients. The aim of this study was to investigate the effect of Robotic gloves versus mirror therapy on Hand function in patients with cerebral vascular accident .


Description:

Post stroke patients aged over 40 years were randomly assigned into three groups (A , B and C ). Group . Maximum hand grip strength and Hand function were assessed before and after the intervention using hand dynamometer and box and block test respectively.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 70
Est. completion date October 11, 2023
Est. primary completion date August 2, 2023
Accepts healthy volunteers No
Gender All
Age group 40 Years to 60 Years
Eligibility Inclusion Criteria: Spasticity level 1 or 1+ according to modified Ashworth scale Exclusion Criteria: Uncontrolled seizures hand fractures or surgery

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Robotic
Patients receive robotic training (grasp and grip)
Mirror
Patients receive mirror therapy
Traditional Physical Therapy
Traditional exercise and Neurophysiological approaches

Locations

Country Name City State
Saudi Arabia Dr. Mariam Salem Jeddah

Sponsors (2)

Lead Sponsor Collaborator
Cairo University Batterjee Medical College

Country where clinical trial is conducted

Saudi Arabia, 

Outcome

Type Measure Description Time frame Safety issue
Primary hand grip strength Hand Dynamometer will be used to evaluate the hand's grip strength 8 weeks
Primary Hand manual function Box and block test for measuring the manual dexterity of patients 8 weeks
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