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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04913506
Other study ID # BYIEAH-H
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 1, 2021
Est. completion date June 1, 2022

Study information

Verified date May 2021
Source Bursa Yüksek Ihtisas Education and Research Hospital
Contact Burcu Metin Ökmen, M.D.Assoc. Prof
Phone +902242955000
Email burcumetinokmen@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this study, it was aimed to evaluate whether or not NMES in front of the mirror brings an additional benefit to mirror therapy alone or NMES alone on upper extremity motor and functional development, spasticity, anxiety, depression, cognitive function and activities of daily living, and neuropathic pain.


Description:

Cerebrovascular diseases are the general name given to clinical neurological pictures that occur as a result of pathological changes in the blood vessels of the primary lesion and / or in the properties of the blood passing through them. Many complications develop in the acute and chronic periods in patients with stroke, and the rate of complication development has been reported to vary between 40-96% in different studies. The aim of hemiplegic upper extremity rehabilitation is to prevent complications and improve lost motor-sensory control. Upper limb rehabilitation is less successful than lower limb rehabilitation because the upper limb is more functional and more complex. For muscle reeducation, NMES is used to strengthen inhibited muscle groups, facilitate voluntary isolated muscle contraction, prevent muscle atrophy, increase metabolism and enzyme activity, change the contractile properties of the muscle, maintain or increase the normal range of motion of the joint, develop voluntary movement and functional gains. NMES has been used in hemiplegia rehabilitation since 1960 for the purpose of functional retraining of muscles. The purpose of this treatment is to enable the muscles with impaired neural function of the electrical current to perform a functional and useful movement. Applications in front of the mirror are thought to trigger the neuronal connections in the motor cortex associated with the imagined movement. Findings obtained from studies with functional magnetic resonance support this theory. Compared to conventional PR, applications in front of the mirror are thought to have more and longer-lasting effects.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date June 1, 2022
Est. primary completion date June 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - Subacute hemiplegia - Patients who can communicate well, are motivated enough and are willing to participate in the study - Patients' medical conditions are stable - Initiation of voluntary extension movement in the wrist (lower limit) Exclusion Criteria: - The presence of more than one previous cerebrovascular disease (except transient ischemic attack). - Presence of flaccid hemiplegia. - Presence of a previous neurological disease causing a decrease in strength in the affected extremity. - Presence of deformity due to a previous fracture, inflammatory arthropathy, etc. in the affected extremity. - Presence of more than grade 3 spasticity in upper extremity according to Modified Ashworth Scale - Use of cardiac pace maker - Presence of fatal cardiac arrhythmia - Presence of seizure history within 2 years.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Group Mirror
For 30 minutes, ROM exercises will be applied to the solid upper extremity in all directions in front of a real mirror by the practitioner. (3 weeks, 5 days a week, 15 sessions in total)
Device:
Group NMES
NMES will be applied to the hemiplegic arm(deltoid, elbow extensors and forearm) for 30 minutes by the practitioner (3 weeks, 5 days a week, 15 sessions in total)
Other:
Group Mirror+NMES
The practitioner will be synchronized with visual or auditory stimuli, and ROM exercises in all directions in front of the real mirror for 30 minutes, and NMES therapy for 30 minutes on the paretic upper extremity will be applied together. (3 weeks, 5 days a week, 15 sessions in total)

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Bursa Yüksek Ihtisas Education and Research Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Fugl-Meyer Upper Extremity Motor Rating Scale To analysis the increase in upper limb motor function Change from Baseline Fugl-Meyer Upper Extremity Motor Rating Scale at 3rd week
Primary Modified Tardieu Scale For spasticity Change from Baseline Modified Tardieu Scale at 3rd week
Primary Modified Ashworth Scale For spasticity Change from Baseline Modified Ashworth Scale at 3rd week
Primary Brunnstrom stages For improvement of upper limb motor function Change from Baseline Brunnstrom stages at 3rd week
Secondary Hospital Anxiety-Depression Scale (HADS) For depression Change from Baseline Hospital Anxiety-Depression Scale at 3rd week
Secondary Mini-Mental Test for cognitive functions Change from Baseline Mini-Mental Test at 3rd week
Secondary Numeric Rating Scale for pain Change from Baseline Numeric Rating Scale at 3rd week
Secondary Pain Detect Questionnaire for neuropathic pain Change from Baseline Pain Detect Questionnaire at 3rd week
Secondary Functional Independence Scale (FIM) for daily life activities Change from Baseline Functional Independence Scale (FIM) at 3rd week
Secondary Ideomotor Apraxia Test for apraxia Change from Baseline Ideomotor Apraxia Test at 3rd week
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