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Orthotic for Parkinson's Disease
N/A
Waitlist Available
Led By Kelly Robb, B.A.Kin, C Ped. (C)
Research Sponsored by Wilfrid Laurier University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
diagnosed with idiopathic Parkinson' disease
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 weeks and 12 weeks post-baseline
Awards & highlights
Study Summary
The purpose of this study is to increase clinical knowledge of the relationship between increased plantar sensory information and orthotics in a Parkinsonian gait. The objectives of this study are to determine if orthotics, with and without a textured top cover, can alter muscle activation, gait parameters, balance, functional mobility, and decrease fall risks in Parkinson's participants.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 weeks and 12 weeks post-baseline
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 weeks and 12 weeks post-baseline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Dynamic Balance, using the Berg Balance Scale, Timed Up and Go, and the Functional Gait Assessment
Change in Postural Sway during Static Stance
Secondary outcome measures
Change in Electromyography (EMG) Activity
Change in Plantar Pressure Distribution
Change in Single Limb Support Time
+3 moreTrial Design
2Treatment groups
Active Control
Group I: OrthoticActive Control1 Intervention
Recruited participants will be asked to wear the customizable foot orthotic, from baseline testing to a follow-up at 6 weeks post-baseline. Outcome measures at 6 weeks will be compared to those at baseline.
Group II: Orthotic+Textured Top CoverActive Control1 Intervention
At 6 weeks post-baseline, participants will received a different orthotic which has a textured material used as its top cover. Testing at 6 weeks post-baseline will determine if acute changes occur as a result of wearing the orthotic with textured top cover. Testing at 12 weeks post-baseline will determine if long-term changes occur as a result of the orthotic with textured top cover.
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Who is running the clinical trial?
Wilfrid Laurier UniversityLead Sponsor
17 Previous Clinical Trials
1,952 Total Patients Enrolled
Kelly Robb, B.A.Kin, C Ped. (C)Principal InvestigatorWilfrid Laurier University
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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