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Effect of Vibro-tactile Stimulation Intensity on Head Posture in Cervical Dystonia

Study acronym: (CD-VTS)
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 3 months later Sep 30, 2026 → Dec 31, 2026
See other at-risk trials from University of Minnesota

Record History

  1. Primary and study completion pushed from Sep 30, 2026 to Dec 31, 2026
    • Secondary endpoints: details revised at 2 of 3 entries
  2. Primary completion pushed from May 2026 to Sep 30, 2026
    • Study completion pushed from Jun 2026 to Sep 30, 2026
    • Start date: Dec 5, 2025 to Mar 10, 2025
    v4
  3. Re-verified, no change to tracked fieldsv3
  4. Start date changed from estimate of Nov 2025 to Dec 5, 2025v2
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The primary goal of this clinical trial is to examine the effects of cervical vibrotactile stimulation intensity on abnormal head posture in people with cervical dystonia. The main question is: Does higher vibration intensity correct head posture to a greater extent than lower vibration intensity? Researchers will compare the head posture of participants with cervical dystonia who receive different intensities of vibration to cervical muscles. The secondary goal of this clinical trial is to examine the degree of proprioceptive impairment in cervical dystonia. Specifically, the study will assess proprioceptive impairment at the neck, wrist, and ankle joints, and seeks to determine whether the impairment improves with cervical vibrotactile stimulation. Researchers will compare the proprioception testing results of these joints between cervical dystonia patients and age- and sex- matched healthy controls. Researchers will also compare the neck proprioception testing results of cervical dystonia patients before and after stimulation. Participants will visit the lab once for three hours, where they will go through: 1. clinical questionnaires; 2. neck, wrist, and ankle proprioception testing, 3. vibrotactile stimulation where they sit and relax 4. neck proprioception testing
Trial Details
NCT Number NCT07245615
Lead Sponsor University of Minnesota
Conditions
(from sponsor)		 Cervical Dystonia
Related terms Torticollis
Enrollment 50 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov