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Correlation of Motor Metrics and Neurological Data (COMMAND)

C

Ceraxis Health

Status

Completed

Conditions

Movement Disorders (Incl Parkinsonism)

Treatments

Diagnostic Test: Ceraxis product

Study type

Observational

Funder types

Industry

Identifiers

NCT05462080
REDD 0001

Details and patient eligibility

About

This is a pilot study to collect data with the Ceraxis product and standard movement disorders tests in order to prove and codify potential correlations.

Enrollment

29 patients

Sex

All

Ages

21+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult with a diagnosis of idiopathic Parkinson's disease or essential tremor by a movement disorders neurologist
  • Age greater than or equal to 21 years
  • Hoehn and Yahr stage I-III
  • Ability to ambulate 200+ meters independently
  • Ability to follow 2-step commands
  • Clinically responsive to medication or Deep Brain Stimulation (DBS)
  • Clinically optimized medication or DBS for at least six months
  • Able to tolerate withdrawal of medication and/or DBS

Exclusion criteria

  • Any comorbidity which would exclude them from being able to use the Ceraxis product
  • Inability to learn how to use the system
  • Diagnosis of dementia or impairment that compromises the ability to provide informed consent
  • Neurological disease other than Parkinson's disease or essential tremor (i.e. multiple sclerosis, stroke with residual motor deficits)
  • Musculoskeletal injury that significantly alters gait

Trial design

29 participants in 1 patient group

Movement Disorders Patients
Treatment:
Diagnostic Test: Ceraxis product

Trial contacts and locations

1

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Central trial contact

Stuart Holtham

Data sourced from clinicaltrials.gov

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