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Clinical Trials/NCT05693207
NCT05693207
Recruiting
Not Applicable

EMG to Detect and Monitor Freezing of Gait Among People With Parkinson's Disease

Tel-Aviv Sourasky Medical Center1 site in 1 country30 target enrollmentOctober 7, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Evaluation of Muscle Contraction in People With PD
Sponsor
Tel-Aviv Sourasky Medical Center
Enrollment
30
Locations
1
Primary Endpoint
Percentage time of co-contractions
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

The main goal of this study is to evaluate, via EMG (electromyography) system, the muscle activity in the lower limbs, to understand the contribution of the muscle activity to FOG (freezing of gait) in Parkinson's patients. The phenomenon of FOG appears in advanced cases of Parkinson's disease (PD) and can lead to an increased risk of falls. There are several approaches claiming that there is abnormal activity in the calf muscles and the freezing events in Parkinson's patients. In the clinic, monitoring FOG is done subjectively, usually through observations or through questionnaires. As a result, the information about the phenomenon may be biased and insensitive. With an electromyographic monitor (EMG), objective information about the muscular activity during normal walking and during unusual events can be obtained.

Detailed Description

The subject will arrive independently at the Tel Aviv Medical Center. After explaining the course of the study and signing a consent form, the subject will be administered the MoCA questionnaire to assess the cognitive state. During this session, the patient will undergo gait evaluation using motion sensors and an EMG device. This meeting will last up to an hour, according to the following breakdown: Explanation of the test (10 min) Preparing the skin (light disinfection with alcohol) for EMG adhesion (10 min.) Performing of the test (20 minutes) Summary and discharge (5 min).

Registry
clinicaltrials.gov
Start Date
October 7, 2021
End Date
December 23, 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Percentage time of co-contractions

Time Frame: 60 minutes

The time of co-contraction during walking will be higher among people with FOG.

Study Sites (1)

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