- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05906875
A Novel Balance Program to Improve Balance in People With Parkinson's Disease
December 17, 2025 updated by: Michael Tautonico, New York Institute of Technology
A Novel Balance Program to Improve Balance in People With Parkinson's Disease: A Feasibility Study
The purpose of this exploratory single-blinded feasibility study is to explore the effects of a lateral stepping program integrated into an existing community-based group exercise program for people with PD.
The researchers hypothesize that participation in a lateral stepping program a minimum of 2 times/week for 8 weeks, in addition to RSB class participation is feasible in middle to late stage PD and will decrease fall risk factors.
The researchers also hypothesize that the integration of this program into an existing community-based RSB program will be deemed feasible as shown by the number of sessions attended by each participant.
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
5
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
-
-
New York
-
Old Westbury, New York, United States, 11568
- New York Institute of Technology
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- A diagnosis of idiopathic PD stages II, III, or IV of the Hoehn and Yahr scale
- 50-85 years inclusive
- Subjects must be enrolled in RSB at NY Tech and attend at least 1 day per week for a minimum of 4 weeks prior to the first baseline assessment
- English speaking.
- Stable PD medication regime.
Exclusion Criteria:
- Any cardiovascular or other medical condition that would affect participation
- Any hip and/or knee surgery or other injury that would prevent full participation in the intervention
- Neurological conditions other than PD
- Montreal Cognitive Assessment of ≤21
- Pain that interferes with testing 13
- Current participation in other strengthening, stretching or balance programs other than Rock Steady Boxing at NY Tech
- Inability to understand and fully participate in this study
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: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: prove feasible to integrate into an existing community group exercise program
Prove feasible to integrate into an existing community group exercise program and Decrease the number of fall risk factors
|
1. Standing hip abduction: Performed without and with resistance bands and/or support.
The participant will raise one leg out to the side and return.
If using a resistance band, one end of the band will be secured to a stable surface and the other end placed around one of the participants' ankles.
The banded leg will be raised to the side.
Three sets of 8-12 repetitions will be performed per side.
2. Lateral stepping: Performed without and with resistance bands.
The participant will perform a series of steps to the side.
If using a resistance band, the band will be placed around both ankles in a 'loop' and the participant will perform the lateral stepping.
Three sets of 8-12 repetitions will be performed per side per subject.
3. Single leg stance: The participant will stand on one leg with support as needed.
The contralateral knee will be held at 45 degrees throughout the exercise.
The instructor will observe to ensure the bent leg does not contact the ground.
Three repetitions of static stance per side will be performed with a goal of 30 seconds, and a maximum time of 60 seconds, per repetition.
5. Lateral Reactive Postural Control: The participant will lean into the researcher's hand to shift their center of mass outside of their base of support.
Hand placement will be at the glenohumeral joint and the pelvis.
The researcher will withdraw support and guard the participant as the participant regains their balance.
This is item 6 on the Mini-BESTest assessment that will be incorporated as an intervention.
To be performed 3x per side.
4. Staggered stance mini-squat: Participants will stand with the feet hip-width apart and one leg placed a short step forward.
The participant will squat straight down keeping the trunk upright and return to an upright position.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Mini-BESTest
Time Frame: 10-15 minutes
|
Performance measure, validated in people with PD, aimed to target and identify 6 different balance control systems
|
10-15 minutes
|
|
The Functional Gait Assessment
Time Frame: 5-20 minutes
|
Validated for people with PD is a performance measure validated in people with PD that is used to assess balance in the higher-functioning older adult and examines ambulation and the ability to perform motor tasks while ambulating
|
5-20 minutes
|
|
The Multidirectional Functional Reach Test
Time Frame: Less than 5 minutes
|
Used to assess stability when displacing a person's balance in a forward, lateral, and backward direction
|
Less than 5 minutes
|
|
The Four-Square Step Test
Time Frame: less than 5 minutes
|
Validated for people with PD is used to measure a patient's fall risk.
The test requires a stopwatch and 4 canes laid in a cross pattern.
The canes crossed pattern makeup 4 quadrants; quadrant 1 (bottom left), quadrant 2 (top left), quadrant 3 (top right), and quadrant 4 (bottom right).
The subject is timed while they step clockwise, and then counterclockwise throughout the quadrants.
An assistive device may be used.
|
less than 5 minutes
|
|
The Activities Balance Confidence Scale
Time Frame: 5-10 minutes
|
Validated for people with PD, is a self-report measure of balance confidence while performing various common activities.
Scale is from 0% to 100% with 100% being the most confident in their balance in a criterion.
|
5-10 minutes
|
|
The Parkinson's Disease Questionnaire-39
Time Frame: approximately 10 minutes
|
39-item self-administered questionnaire designed to assess 8 different quality-of-life domains.
Uses a 5-point ordinal scale with 0 being never and 5 being always.
Lower scores indicate a lower quality of life.
|
approximately 10 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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)
September 20, 2023
Primary Completion (Actual)
December 18, 2023
Study Completion (Actual)
December 18, 2023
Study Registration Dates
First Submitted
June 7, 2023
First Submitted That Met QC Criteria
June 7, 2023
First Posted (Actual)
June 18, 2023
Study Record Updates
Last Update Posted (Actual)
December 19, 2025
Last Update Submitted That Met QC Criteria
December 17, 2025
Last Verified
December 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- BHS- IRB
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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