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CompletedNCT07687732Updated Jul 7, 2026

Vibrotactile Stimulation for Parkinson's Disease

An Early Phase 1 interventional study of Vibrotactile stimulation in PARKINSON DISEASE (Disorder), sponsored by University of Colorado, Denver. Completed at 1 site in United States. Open to participants aged 18 Years to 85 Years. Per ClinicalTrials.gov, last updated 2026-07-07.

Sponsored by University of Colorado, Denver · Early Phase 1, Interventional, and Basic science

From the registry’s dates

  • Registered 2 years 10 months after the study started (first participant enrolled Aug 2023, registered Jun 2026).
Phase
Early Phase 1
Study type
Interventional
Enrollment
12
Allocation
Randomized
Ages
18 Years to 85 Years
Sex
All
01

Study summary

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

Read the detailed description

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.

02

Conditions studied

  • PARKINSON DISEASE (Disorder)

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Keywords

  • Parkinson's disease
  • non-invasive stimulation
  • vibrotactile stimulation
03

In context

Parkinson Disease

4,487 studies on the registry are indexed under Parkinson Disease; 1,082 are open to participants now.

This study's enrollment of 12 is below the median of 40 across 3,294 interventional studies indexed under Parkinson Disease.

Browse Parkinson Disease studies →

Lead sponsor

University of Colorado, Denver is the lead sponsor of 1,499 studies on the registry; 315 are open to participants now.

Of its 139 completed or terminated interventional studies of FDA-regulated products, 89 (64%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

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.
05

Study design

Phase
Early Phase 1
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
12 participants (actual)

Study arms

  • Experimental
    RVS and All-on sequence

    Participants receives the RVS stimulation pattern followed by the All-on pattern

    Device: Vibrotactile stimulation

  • Experimental
    All-on and RVS sequence

    Participants receives the All-on stimulation pattern followed by the RVS pattern

    Device: Vibrotactile stimulation

Interventions

  • DeviceVibrotactile stimulation

    Vibration patterns applied on the fingertips.

06

What researchers measure

Primary outcomes

  1. Beta band power

    13-30 Hz frequency band

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

Secondary outcomes

  1. MDS-UPDRS Part III

    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).

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

07

Study locations

1 site
  • CTRC Space, Health Sciences Building
    Denver, Colorado 80045, United States
08

References and documents

Individual participant data

Plan to share: Yes — All de-identified data will be shared on github.

Supporting information: Study protocol, Sap, Icf, Csr, Analytic code

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 7, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07687732
Lead sponsor
University of Colorado, Denver
Responsible party
Sponsor
First posted
Jul 7, 2026
Start date
Aug 23, 2023
Primary completion
Aug 12, 2025
Completion
Aug 16, 2025
Last update
Jul 7, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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