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Completed

NCT Number: NCT07687732

Vibrotactile Stimulation for Parkinson's Disease

Investigation on whether and how vibrotactile stimulation applied on the fingertips affects beta power in the subthalamic nucleus.

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Key information

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

CTRC Space, Health Sciences Building

Denver, Colorado, 80045, United States

About this study

With a randomized order, two stimulation patterns are applied for one hour each on the fingertips of Parkinson's patients with deep brain stimulation, while periodically recording from subthalamic nucleus (STN) local field potentials (LFPs). The randomized vibrotactile stimulation (RVS) power is expected to reduce neuronal synchronization and LFP beta power. The All-on stimulation pattern is not expected to reduce neuronal synchronization and LFP beta power.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • The population to be enrolled will be between 18 and 85 years of
  • Have a diagnosis of idiopathic Parkinson's disease, determined by a movement disorders neurologist at the CU Movement Disorders Center
  • Has undergone deep brain stimulation surgery at the University of Colorado hospital

Exclusion criteria

  • have severe sensory abnormalities of the fingertips such as vibratory urticaria
  • Patients that cannot clearly communicate with staff and speak English
  • Patients that are on psychoactive or narcoleptic medications, medications that affect brain function or alter EEG recorded activity (i.e., anticonvulsants, ADHD, depression, or anxiety medication)
  • Participation in another drug, device, biologic, or intervention trial concurrently or within the preceding 30 days.

Treatment and study plan

Vibrotactile Stimulation

Device

Vibration patterns applied on the fingertips.

Primary outcomes

  1. Beta band power

    Time frame: At baseline (pre-intervention) and after 30 min of intervention

    13-30 Hz frequency band

Secondary outcomes

  1. MDS-UPDRS Part III

    Time frame: At baseline (pre-intervention) and 1-hour of intervention

    Movement disorder assessment for Parkinson's disease motor symptoms of the upper extremity. The scale is from 0 to 4 for the items in the MDS-UPDRS Part III, where 0 represents normal function (and 4 is worse).

Sponsors and collaborators

Lead sponsor

University of Colorado, Denver

Other

Registry information

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Jul 7, 2026
Registry last updated
Jul 7, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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