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Augmented Reality Treadmill Training in Patients With Parkinson's Disease

Augmented Reality Treadmill Training in Patients With Parkinson's Disease: a Randomized Controlled Study

Status
Terminated
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04108741
Acronym
Falls_in_PD
Enrollment
39
Registered
2019-09-30
Start date
2020-09-15
Completion date
2025-06-10
Last updated
2026-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fall, Parkinson Disease

Keywords

Parkinson Disease

Brief summary

Gait disorder is a disabling symptom in Parkinson's disease (PD) affecting all patients during the course. Three methods of treadmill training (TT) will be compared to assess additional augmented reality (AR), or additional dual task (DT). AR TT, DT TT, and TT alone applied over 3 weeks at each day will be compared for their impact on falls, walking, freezing and attention for 3 months in a double blinded randomized controlled trial during regular neurorehabilitation.

Interventions

DEVICEC-Mill augmented reality treadmill training

PD Patients will be randomized to treadmill training with augmented reality or to treadmill training with random number generation or to treadmill training for 3 weeks at 5 days a week for 30 minutes.

Sponsors

Klinik Valens
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
35 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* Informed Consent as documented by signature * Parkinson´s disease without dementia and hallucination * at least one fall within the past 3 months or postural instability * Gait disorder * Hoehn and Yahr stages II-IV * able to perform the treadmill therapy during a study

Exclusion criteria

* Contraindications to treadmill therapy (e.g. hip fracture) * Dementia as defined by an Montreal cognitive assessment (MOCA) \< 20

Design outcomes

Primary

MeasureTime frameDescription
Frequency of falls3 months before study to 3 months following the studygroup difference of the difference in falls

Secondary

MeasureTime frameDescription
Secondary outcomes:before and after the training period of 3 weeksFreezing of Gait (FOG) Questionnaire
Sensor based gait analysesbefore and after the training period of 3 weeks and after 3 monthsfor one week

Countries

Switzerland

Contacts

PRINCIPAL_INVESTIGATORVeit Mylius, Prof. Dr.

Department of Neurology, Kliniken Valens

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 11, 2026