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Clinical Trials/NCT05815823
NCT05815823
Completed
Not Applicable

The Effect of Virtual Reality Assisted Upper Extremity Robotic Therapy on Pain, Daily Living Activities and Functional Status in Patients With Stroke

Istanbul Physical Medicine Rehabilitation Training and Research Hospital0 sites40 target enrollmentJanuary 1, 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
the Effect of Virtual Reality on Stroke Rehabilitation
Sponsor
Istanbul Physical Medicine Rehabilitation Training and Research Hospital
Enrollment
40
Primary Endpoint
FMA-UE scale
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The purpose of this study is to determine how adding virtual reality assisted robotic treatment to traditional rehabilitation affects stroke patients' pain levels, functional status, and daily living activities.After conventional and robotic therapy Each patient was evaluated The Barthel Index (BI), the Fugl Meyer Assessment Upper Extremity (FMA-UE), and the Visual Analogue Scale (VAS) were used to assess the patients' pain, daily living activities, and upper extremity motor function.

Detailed Description

The purpose of this study is to determine how adding virtual reality assisted robotic treatment to traditional rehabilitation affects stroke patients' pain levels, functional status, and daily living activities. Materials and Methods: The study included 40 stroke patients. Two groups of patients were created. Group I also underwent 20 sessions of upper extremity robot-assisted therapy for 4 weeks, 5 days a week, for 30 minutes per session, in addition to receiving conventional therapy (5 days a week for 4 weeks, 1 hour each day). Group II only got traditional therapy. Each patient was assessed both before and after the procedure. The Barthel Index (BI), the Fugl Meyer Assessment Upper Extremity (FMA-UE), and the Visual Analogue Scale (VAS) were used to assess the patients' pain, daily living activities, and upper extremity motor function.

Registry
clinicaltrials.gov
Start Date
January 1, 2015
End Date
January 1, 2017
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Istanbul Physical Medicine Rehabilitation Training and Research Hospital
Responsible Party
Principal Investigator
Principal Investigator

Canan Avcı

Specialist of physical medicine and rehabilitation

Istanbul Physical Medicine Rehabilitation Training and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • Ischemic or hemorhagic hemiplegia
  • Brunnstrom upper extremity motor stage ≥3
  • At least 3 months have passed
  • Modified Ashworth Score ≤2
  • 18-85 year old patients with diagnosis of stroke

Exclusion Criteria

  • Cognitive impairment
  • mini mental test \<24
  • deformity and / or contracture in the upper extremity
  • Patients diagnosed with KBAS

Outcomes

Primary Outcomes

FMA-UE scale

Time Frame: after treatment (1 month)

FMA-UE evaluates the hemiparetic arm's mobility, including reflexes, the presence of synergies, and each of the upper limb's independent motions, including grasp. The dysmetria, coordination, and velocity of the patient are also evaluated using items on this scale. It is intended to assess muscle strength, reflex actions, and movement control in the upper extremity following a stroke. It has 33 elements and accepts values ranging from 0 to 2. Scores under 31 suggest a weak upper extremity, scores between 32 and 47 show a restricted upper extremity, scores between 48 and 52 indicate a noteworthy upper extremity, and scores between 53 and 66 indicate a full upper extremity.

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