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Clinical Trials/NCT05485740
NCT05485740
Completed
Not Applicable

Cognitive Multisensory Rehabilitation on Upper Extremity Function in Stroke Patients

October 6 University1 site in 1 country30 target enrollmentAugust 1, 2022
ConditionsStroke

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke
Sponsor
October 6 University
Enrollment
30
Locations
1
Primary Endpoint
Action research arm test
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

PURPOSE:

To investigate the effect of cognitive multisensory rehabilitation program on upper extremity function in stroke patients.

BACKGROUND: Cognitive Multisensory Rehabilitation (CMR) is a promising therapy for upper limb recovery in stroke, as the CMR considered an effective therapy for motor recovery for adults with stroke

Detailed Description

Thirty patients with stroke The patients will randomly be divided into two equal groups; the control group which received the selected exercise program and the study group received the same exercise training program in addition to cognitive multisensory rehabilitation program, three times per week for 2 months. The evaluation methods Action research arm test (ARAT), Fugl-Myer Assessment upper extremity (FMA-UE), manual function test and Motor Evaluation Scale for Upper Extremity

Registry
clinicaltrials.gov
Start Date
August 1, 2022
End Date
December 30, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Lama Saad El-Din Mahmoud

Lecturer of physical therapy, Department of Neuromuscular disorders and its surgery, faculty of physical therapy, october 6 univerisity

October 6 University

Eligibility Criteria

Inclusion Criteria

  • Thirty hemiplegic patients, with the onset of stroke six months or longer.
  • Both sexes, with ages ranging from 45:
  • Body mass index will range from 18.5-to 29.9 Kg/m2.

Exclusion Criteria

  • Other brain injuries/illnesses, cognitive impairment, severe sensory or proprioceptive loss.
  • Other causes of hemiplegia.
  • Other causes of upper extremity dysfunction.

Outcomes

Primary Outcomes

Action research arm test

Time Frame: 8 weeks

one of the most commonly used upper limb outcomes that measure the activity level in stroke rehabilitation studies consists of a total of 19 functional materials and four subtests as follows: grasp, grip, pinch, and gross movement

Manual function test

Time Frame: 8 weeks

is a performance-based assessment for upper limbs with paresis caused by stroke The MFT is graded on a four-level scale. The total MFT score can range from 0 (severely impaired) to 32 (full function)

Fugl Myer Assessment upper extremity

Time Frame: 8 weeks

is a scale consisting of 30 items assessing motor function and 3 items assessing reflex function The FMA-UE scores of 0 through 22 represent no upper-limb capacity; scores of 23 through 31 represent poor capacity; scores of 32 through 47 represent limited capacity; scores of 48 through 52 represent notable capacity; and scores of 53 through 66 represent full upper-limb capacity, total sensation UE score 12, passive joint motion UE score 24 and UE joint pain scores 24

Motor Evaluation Scale for Upper Extremity in Stroke patients

Time Frame: 8 weeks

is a scale that measures the quality of movement of the hemiparetic upper extremity The maximum total score for the MESUPES is 58. The MESUPES-arm comprises 8 items of shoulder and elbow performance, with a maximum score of 40. Each item is scored from 0 (inability to adapt muscle tone to the movement) to 5 (ability to correct and complete motion without help)

Study Sites (1)

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