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COMPLETED NA

Effects Compressive Tissue Flossing on Lateral Elbow Tendinopathy in US Service Members

NCT06369701 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this research study will be to assess the effects of a compressive tissue flossing (CTF) program on the symptoms of lateral elbow tendinopathy in United States service members. Dependent variables will be the Defense and Veteran's Pain Rating Scale (DVPRS), decrease their Patient-Rated Tennis Elbow Evaluation (PRTEE) score, increase their maximal grip strength in the affected upper extremity (UE). Measurements will be taken at baseline, immediately after the first CTF intervention, and at the 1-week follow-up, for a total of 3 measurements.

Conditions Studied

Interventions

  • DEVICE Compressive tissue floss band

Study Locations (1)

Texas

  • Brooke Army Medical Center — Fort Sam Houston

Trial Details

FieldValue
Enrollment Target 35 participants
Start Date 2024-02-13
Est. Completion 2024-05-01
Phase NA

Sponsor

Brooke Army Medical Center

18 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06369701

The ClinicalTrials.gov registry entry for NCT06369701 describes a study currently listed as completed. 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 35 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Brooke Army Medical Center, which has 18 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Lateral Elbow Tendinopathy appearing as the primary indexed condition, and to 1 intervention — of which Compressive tissue floss band 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: NCT06369701 reports 1 study location spanning 1 distinct geographic area — top geographies include Texas. 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 NCT06369701 about?

NCT06369701 is a clinical study titled "Effects Compressive Tissue Flossing on Lateral Elbow Tendinopathy in US Service Members". The purpose of this research study will be to assess the effects of a compressive tissue flossing (CTF) program on the symptoms of lateral elbow tendinopathy in United States service members. Dependent variables will be the Defense and Veteran's Pain Rating Scale (DVPRS), decrease their Patient-Rate...

What is the current status of trial NCT06369701?

This trial is currently completed. It is a NA study. The enrollment target is 35 participants. The study started on 2024-02-13. Estimated completion is 2024-05-01.

What conditions does trial NCT06369701 study?

This clinical trial studies the following conditions: Lateral Elbow Tendinopathy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06369701?

The interventions under investigation include: Compressive tissue floss band (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06369701?

This trial is sponsored by Brooke Army Medical Center, which has 18 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06369701 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial