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NCT07245615 · ClinicalTrials.gov registry record · NA
Effect of Vibro-tactile Stimulation Intensity on Head Posture in Cervical Dystonia
A NA study of Cervical Dystonia, sponsored by University of Minnesota.
- Recruiting
- Registry status
- NA
- Development phase
- 50
- Enrollment target
- 1
- Study location
NCT07245615: Recruiting NA study of Cervical Dystonia, sponsored by University of Minnesota.
NCT07245615 is a NA study of Cervical Dystonia that is actively recruiting participants, run by University of Minnesota. The registered enrollment target is 50 participants, below the 84-participant average among 15 other Cervical Dystonia trials with a reported enrollment target (40% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07245615, a NA study of Cervical Dystonia, is actively recruiting participants, sponsored by University of Minnesota.
- RECRUITING
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
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
Primary Outcome
The primary outcome measure is the head angle index, which quantifies how much a participant's head posture deviates from a neutral upright position. There are three degrees of freedom for the neck joint (axial rotation, lateral bending, and flexion/extension). For each participant, the degree(s) of freedom with abnormality will be identified at baseline. For any time period during the experiment, the mean absolute neck angle in each abnormal degree of freedom will be calculated and normalized b
Conditions Studied
Interventions
- DEVICE cervical vibrotactile stimulation
Study Locations (1)
Minnesota
- Human Sensorimotor Control Laboratory - Minneapolis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2025-12-05 |
| Est. Completion | 2026-06 |
| Phase | NA |
What NCT07245615 shows while recruiting
NCT07245615 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 84-participant average among 15 other Cervical Dystonia trials with a reported enrollment target (40% lower).
The record links to 1 condition, with Cervical Dystonia appearing as the primary indexed condition, and to 1 intervention - of which cervical vibrotactile stimulation is the first listed.
NCT07245615 reports a single indexed study location in Minnesota.
Frequently Asked Questions
What is clinical trial NCT07245615 about?
NCT07245615 is a clinical study titled "Effect of Vibro-tactile Stimulation Intensity on Head Posture in Cervical Dystonia". 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? R...
What is the current status of trial NCT07245615?
This trial is currently recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2025-12-05. Estimated completion is 2026-06.
What conditions does trial NCT07245615 study?
This clinical trial studies the following conditions: Cervical Dystonia.
What interventions are being tested in trial NCT07245615?
The interventions under investigation include: cervical vibrotactile stimulation (DEVICE).
Who is sponsoring clinical trial NCT07245615?
This trial is sponsored by University of Minnesota, which has 966 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07245615 being conducted?
This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT07245615's enrollment target sits among peer trials
50 7th of 15 higher than 9 of 15 other Cervical Dystonia trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Cervical Dystonia trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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