- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07399613
Effects of Protective Step Training on Proactive and Reactive Motor Adaptations in Parkinson's Disease Patients
February 3, 2026 updated by: Arizona State University
The aim of this study was to investigate to what extent PD affects the ability to walk, respond to balance perturbations (i.e., Protective Step Training) and produce acute short-term effects to improve compensatory reactions and control of unperturbed walking balance.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Understanding the mechanism of compensation and neuroplasticity to unexpected step perturbation training during walking and static stance can have positive implications on the treatment of PD by helping to design effective training paradigms that remediate fall risk.
Current rehabilitation therapies are inadequate at reducing falls in people with Parkinson's disease (PD).
While pharmacologic and surgical treatments have proved largely ineffective in treating postural instability and gait dysfunction in people with PD, studies have demonstrated that therapy specifically focusing on posture, gait, and balance may significantly improve these factors and reduce falls.
The primary goal of this study was to assess the effectiveness of a novel and promising intervention therapy (protective step training - i.e., PST - balance disturbance/perturbation during treadmill walking) to improve balance as measured by the reaction time and reduce falls in people with PD.
A secondary goal was to understand the effects of PST on proactive and reactive feedback responses during stance and gait tasks.
Multi-baseline, repeated measures analyses were performed on the multitude of proactive and reactive performance measures to assess the effects of PST on gait and postural stability parameters.
Study Type
Interventional
Enrollment (Actual)
12
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Arizona
-
Glendale, Arizona, United States, 85302
- Glencroft Senior Living: Retirement Community in Arizona
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- able to ambulate without assistance
- had no known neurologic, cardiovascular, or orthopedic deficit - (Mini-Mental Status Examination <25), and had a Hoehn & Yahr (H&Y) score between II-III.
Exclusion Criteria:
- exhibited functionally disabling dyskinesia
- has dystonia, orthostatic hypotension,
- had neurosurgical intervention (deep brain stimulation)
- has and any significant musculoskeletal or metabolic disorders.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Standing Perturbation Protocol
Different postural perturbations were administered - while walking and while standing.
|
Perturbation during standing and walking to actively assess proactive as well as reactive motor adaptations.
Other Names:
|
|
Experimental: Walking Perturbation Protocol
Different postural perturbations were administered - while walking and while standing.
|
Perturbation during standing and walking to actively assess proactive as well as reactive motor adaptations.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Joint (knee) reaction time
Time Frame: one year
|
Joint (knee) Reaction time during standing and walking perturbations.
|
one year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 19, 2022
Primary Completion (Actual)
January 18, 2023
Study Completion (Actual)
March 18, 2023
Study Registration Dates
First Submitted
December 12, 2024
First Submitted That Met QC Criteria
February 3, 2026
First Posted (Actual)
February 10, 2026
Study Record Updates
Last Update Posted (Actual)
February 10, 2026
Last Update Submitted That Met QC Criteria
February 3, 2026
Last Verified
May 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- STUDY00015237
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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