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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.
Full 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.
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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
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Interventional model
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30 participants in 1 patient group
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Central trial contact
Tatyana Gurevich, Prof; Marina Brozgol, MS
Data sourced from clinicaltrials.gov
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