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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 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.
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
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 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07245615
The ClinicalTrials.gov registry entry for NCT07245615 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 84-participant average among 15 other Cervical Dystonia trials with a reported enrollment target (40% lower). The listed sponsor is University of Minnesota, which has 966 total studies on file at ClinicalTrials.gov.
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 1 study location spanning 1 distinct geographic area - top geographies include 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.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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