- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07380737
Feasibility and Preliminary Effects of the Walking Tall App for Home-Based Gait Training in Parkinson's Disease: A Pilot Study
February 12, 2026 updated by: Tel-Aviv Sourasky Medical Center
This is a pilot study designed to assess the feasibility, adherence, and preliminary effects of a 6-week home-based gait training intervention using the Walking Tall mobile app in individuals with Parkinson's disease.
The app delivers rhythmic auditory cues and motivational verbal prompts to promote gait improvements.
Primary outcomes include daily walking duration and step count measured via wearable sensors; secondary outcomes include gait speed, balance, self-reported confidence, and usability.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
This open-label, single-arm feasibility study will recruit 30 participants with idiopathic Parkinson's disease, currently enrolled in a rehabilitation program at the Ezra LeMarpe Organization in Israel.
Participants will perform 4-5 walking sessions per week for 6 weeks using the Walking Tall smartphone application.
The app delivers rhythmic cueing and motivational prompts to enhance walking speed, stride length, and confidence.
The study includes baseline and post-intervention assessments.
Walking behavior will be monitored using a tri-axial accelerometer worn for 7 days at each timepoint.
The primary aim is to evaluate feasibility, adherence, and changes in daily walking activity, with secondary outcomes addressing gait parameters and user satisfaction.
Findings will guide the design of future randomized controlled trials.
Study Type
Interventional
Enrollment (Estimated)
30
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 Contact
- Name: Marina Brozgol, MS
- Phone Number: +972-3-6947514
- Email: marinab@tlvmc.gov.il
Study Contact Backup
- Name: Tatyana Gurevich, Prof
- Email: tanyag@tlvmc.gov.il
Study Locations
-
-
-
Tel Aviv, Israel, 6423906
- Recruiting
- Tel Aviv Sourasky Medical Center (Ichilov Hospital)
-
Contact:
- Sourasky Medical Cente
- Phone Number: +972-3-6974000
- Email: ichilov-intru@tlvmc.gov.il
-
-
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:
- Clinical diagnosis of idiopathic Parkinson's disease (MDS criteria);
- Hoehn & Yahr stage II-III (ON-medication state);
- Able to walk independently for ≥5 minutes;
- Stable medication for ≥1 month;
- Currently enrolled in a rehab program at Ezra LeMarpe;
- Able to provide written informed consent;
Exclusion Criteria:
- Musculoskeletal, neurological, or visual/hearing impairments affecting gait;
- Cognitive impairments or severe behavioral symptoms;
- History of stroke, severe TBI, or brain tumor;
- Cardiovascular contraindications;
- Inability to use a smartphone;
- Participation in other concurrent intervention studies.
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 |
|---|---|
|
Experimental: Walking Tall App Intervention
Participants will use the Walking Tall smartphone app to complete 4-5 home-based walking sessions per week for 6 weeks.
The app provides rhythmic auditory cues and verbal prompts to improve gait quality.
|
Participants will use the Walking Tall smartphone app to complete 4-5 home-based walking sessions per week for 6 weeks.
The app provides rhythmic auditory cues and verbal prompts to improve gait quality.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Average Step Count Per Day
Time Frame: Time Frame: Baseline and 6 weeks
|
Measured via accelerometer
|
Time Frame: Baseline and 6 weeks
|
|
Daily Walking Duration (minutes/week)
Time Frame: Time Frame: Baseline and 6 weeks
|
Measured using tri-axial accelerometer (Axivity) over 7 days
|
Time Frame: Baseline and 6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Gait Speed (m/s) - single- and dual-task
Time Frame: Time Frame: Baseline and 6 weeks
|
Assessed using a 1-minute walking test under two conditions: (1) single-task (normal walking) and (2) dual-task (walking while performing a cognitive task such as serial subtraction).
Gait speed is calculated in meters per second based on distance walked over time in each condition.
|
Time Frame: Baseline and 6 weeks
|
|
Short Physical Performance Battery (SPPB)
Time Frame: Time Frame: Baseline and 6 weeks
|
The SPPB is a standardized test that evaluates lower extremity function using three components: balance (side-by-side, semi-tandem, tandem stance), gait speed over a 4-meter walk, and chair stands.
Each component is scored from 0 to 4, with a total score ranging from 0 (worst performance) to 12 (best performance).
|
Time Frame: Baseline and 6 weeks
|
|
Timed Up and Go (TUG) - single- and dual-task
Time Frame: Time Frame: Baseline and 6 weeks
|
The TUG test measures functional mobility by timing how long it takes a participant to stand up from a chair, walk 3 meters, turn, return, and sit down.
It is performed under two conditions: (1) single-task (normal walking) and (2) dual-task (walking while performing a cognitive task, such as serial subtraction).
The test evaluates gait, balance, and cognitive-motor integration.
|
Time Frame: Baseline and 6 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-reported questionnaires: Activities-specific Balance Confidence (ABC)
Time Frame: Time Frame: Baseline and 6 weeks
|
Activities-specific Balance Confidence (ABC) Scale A 16-item self-report questionnaire assessing participants' confidence in performing various daily activities without losing balance or becoming unsteady.
Scores range from 0% (no confidence) to 100% (complete confidence), with higher scores indicating greater balance confidence.
|
Time Frame: Baseline and 6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Tatyana Gurevich, Prof, Head of the Movement Disorders Unit at Ichilov Hospital
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.
General Publications
- Brodie, M. A., & University of New South Wales. (2023, August 7). New app is a step towards helping people with Parkinson's disease walk more confidently. UNSW Newsroom. Retrieved from https://www.unsw.edu.au/newsroom/news/2023/08/new-app-is-a-step-towards-helping-people-with-parkinsons-disease
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)
December 29, 2025
Primary Completion (Estimated)
August 31, 2026
Study Completion (Estimated)
December 31, 2026
Study Registration Dates
First Submitted
January 25, 2026
First Submitted That Met QC Criteria
January 25, 2026
First Posted (Actual)
February 2, 2026
Study Record Updates
Last Update Posted (Actual)
February 13, 2026
Last Update Submitted That Met QC Criteria
February 12, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0481_25_TLV_TG
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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