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Tactile cueing as a means to oppose gait impairments deriving from Parkinson*s disease<br>

Completed
Conditions
Festinating gait
walking impairment
10028037
Registration Number
NL-OMON45512
Lead Sponsor
Medisch Spectrum Twente
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
10
Inclusion Criteria

- The patient exhibits gait impairments caused by Parkinson*s disease
- Patients' age is over 18 years
- Able to visit the neurology clinic at MST Enschede

Exclusion Criteria

- Unable to provide written informed consent
- Exhibits gait impairments as a result of any other factor than Parkinson*s disease
- Significant cognitive deterioration that causes the patient to be unable to understand the research purpose and accompanying instructions

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The main parameter is the time it takes for the patient to complete the<br /><br>prescribed walking test. The results of the repeated tests will be compared to<br /><br>see if improvements can be ascribed to situations (e.g. walking with/without<br /><br>device). </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>There are two secondary study parameters, namely the number of freezing<br /><br>episodes the subject experiences, and secondly the number of steps (step<br /><br>length) the subjects exhibits during testing. Value will be allotted to these<br /><br>secondary parameters by comparing the repeated tests in which the situation was<br /><br>altered (e.g. walking with/without device).<br /><br><br /><br>Additional study parameters will consist of:<br /><br>o Age<br /><br>o Sex<br /><br>o Score on Hoehn and Yahr scale<br /><br>o Medication state (ON/OFF)<br /><br>o Outcome of the freezing of gait questionnaire<br /><br>These study parameters will be assessed during the anamnesis.</p><br>
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