NeuroGlove PD Study Clinical

Completed · Early Phase 1

Conditions studied: Parkinson Disease

In brief

Safety and Feasibility of Peripheral Sensory Stimulation of the Hand in the Treatment of Parkinson's Disease

Key facts

Study ID

NCT06578273

Run by

NeuroGlove LLC

People needed

8

Starts

2024-08-22

Expected to finish

2024-08-22

Last updated by the study team

2024-09-03

Who can join

Age: 18 and older, up to 85. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Able to and willing to provide informed consent. Legally authorized representatives (LARs) will not be allowed to consent on behalf of the subject.
• Men and women ≥18 and <85 years of age.
• Carry an active diagnosis of PD
• Suffer from PD symptoms that impact subject's daily activities and quality of life

You may not qualify if…

• Physical limitations of the upper extremity (e.g., fracture, joint deformity, severe spasticity/contracture, wounds, skin breakdown, lymphedema, etc.)
• Lacks the ability to comprehend or follow instructions, or for any reason, in the opinion of the investigator, would be unlikely or unable to comply with study protocol requirements.
• Currently participating in another interventional clinical trial (observational clinical trial participation is allowed for study enrollment.)

Where it is running

• NeuroGlove — Minneapolis, Minnesota, United States

Full record on ClinicalTrials.gov

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