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

Tactile cueing as a means to oppose gait impairments deriving from Parkinson*s disease - Tactile cueing

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON45512
Enrollment
10
Registered
2017-05-18
Start date
2017-07-05
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Festinating gait walking impairment

Interventions

The intended intervention is described as follows: A prompt will be offered by providing an alternating vibration underneath either foot of the subject by using the prototype. The frequency of the rh
Gait impairments
Parkinson
Tactile

Sponsors

Medisch Spectrum Twente
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
The main parameter is the time it takes for the patient to complete the prescribed walking test. The results of the repeated tests will be compared to see if improvements can be ascribed to situations (e.g. walking with/without device).

Secondary

MeasureTime frame
There are two secondary study parameters, namely the number of freezing episodes the subject experiences, and secondly the number of steps (step length) the subjects exhibits during testing. Value will be allotted to these secondary parameters by comparing the repeated tests in which the situation was altered (e.g. walking with/without device). Additional study parameters will consist of: o Age o Sex o Score on Hoehn and Yahr scale o Medication state (ON/OFF) o Outcome of the freezing of gait questionnaire These study parameters will be assessed during the anamnesis.

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)