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PD vitamin supplementation for Parkinson's Disease
N/A
Waitlist Available
Led By William G Werner, PT, EdD
Research Sponsored by New York Institute of Technology
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 weeks
Awards & highlights
Study Summary
This experiment seeks to determine whether individuals with PD will benefit from vitamin B6 (pyridoxine hydrochloride), B12 (cyanocobalamin), and Folic Acid supplementation, whether they will benefit from a 6-week circuit training program, or whether they will benefit from a combination of the two interventions. The outcome variables will include: plasma homocysteine, GSH:GSSG ratio, cognitive function, balance, strength, functional activities, kinematic gait analysis, and a quality of life questionnaire.
Eligible Conditions
- Parkinson's Disease
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Balance
GSH:GSSG ratio
Kinematic gait analysis
+7 moreTrial Design
4Treatment groups
Experimental Treatment
Active Control
Group I: PD vitamin supplementationExperimental Treatment1 Intervention
Group II: PD vitamin + exerciseExperimental Treatment1 Intervention
Group III: PD exercise interventionExperimental Treatment1 Intervention
Group IV: PD controlActive Control1 Intervention
Find a Location
Who is running the clinical trial?
New York Institute of TechnologyLead Sponsor
51 Previous Clinical Trials
2,031 Total Patients Enrolled
Stony Brook UniversityOTHER
213 Previous Clinical Trials
39,487 Total Patients Enrolled
William G Werner, PT, EdDPrincipal InvestigatorNew York Institute of Technology, New York College of Osteopathic Medicine
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