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Self-Myofascial Release of the Upper Cervical Muscles
NCT06529991 · View on ClinicalTrials.gov ↗
Study Summary
The primary objective is to examine the influence of the suboccipital muscles on the superficial back line. The investigators will measure the following as part of this objective: * Changes in biomechanical and viscoelastic properties of points within the superficial back fascial train measured by a handheld myotonometer. * Pain pressure threshold measured by algometry. * Ankle range of motion. * Foot plantar pressure changes. All participants will have a 5-minute self-myofascial release intervention.
Conditions Studied
Interventions
- DEVICE Occipivot suboccipital pillow self-myofascial release
Study Locations (1)
Alabama
- Edward Via College of Osteopathic Medicine-Auburn — Auburn
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2024-06-26 |
| Est. Completion | 2026-04-26 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06529991
The ClinicalTrials.gov registry entry for NCT06529991 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Edward Via Virginia College of Osteopathic Medicine, which has 7 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Suboccipital Muscles appearing as the primary indexed condition, and to 1 intervention — of which Occipivot suboccipital pillow self-myofascial release is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06529991 reports 1 study location spanning 1 distinct geographic area — top geographies include Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06529991 about?
NCT06529991 is a clinical study titled "Self-Myofascial Release of the Upper Cervical Muscles". The primary objective is to examine the influence of the suboccipital muscles on the superficial back line. The investigators will measure the following as part of this objective: * Changes in biomechanical and viscoelastic properties of points within the superficial back fascial train measured by ...
What is the current status of trial NCT06529991?
This trial is currently recruiting. It is a NA study. The enrollment target is 30 participants. The study started on 2024-06-26. Estimated completion is 2026-04-26.
What conditions does trial NCT06529991 study?
This clinical trial studies the following conditions: Suboccipital Muscles, Superficial Back Line, Myofascial Release. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06529991?
The interventions under investigation include: Occipivot suboccipital pillow self-myofascial release (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06529991?
This trial is sponsored by Edward Via Virginia College of Osteopathic Medicine, which has 7 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06529991 being conducted?
This trial has 1 study location across Alabama. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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