Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING NA

Examining the Most Effective Method to Reduce Running Ground Contact Time

NCT06988709 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of our study is to establish the most effective running retraining technique to decrease ground contact time. This will be investigated by applying three running retraining conditions and assessing the change in ground contact time and other biomechanical variables between the runner's baseline running and each retraining technique.

Conditions Studied

Interventions

  • OTHER Real-time Visual Feedback
  • OTHER Real-time Auditory Feedback
  • OTHER Real-time Verbal Feedback

Study Locations (1)

New York

  • Keller Army Community Hospital — West Point

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2025-05-01
Est. Completion 2026-12-01
Phase NA

Sponsor

Keller Army Community Hospital

4 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06988709

The ClinicalTrials.gov registry entry for NCT06988709 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 Keller Army Community Hospital, which has 4 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 Healthy Runners appearing as the primary indexed condition, and to 3 interventions — of which Real-time Visual Feedback 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: NCT06988709 reports 1 study location spanning 1 distinct geographic area — top geographies include New York. 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 NCT06988709 about?

NCT06988709 is a clinical study titled "Examining the Most Effective Method to Reduce Running Ground Contact Time". The purpose of our study is to establish the most effective running retraining technique to decrease ground contact time. This will be investigated by applying three running retraining conditions and assessing the change in ground contact time and other biomechanical variables between the runner's b...

What is the current status of trial NCT06988709?

This trial is currently recruiting. It is a NA study. The enrollment target is 30 participants. The study started on 2025-05-01. Estimated completion is 2026-12-01.

What conditions does trial NCT06988709 study?

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

What interventions are being tested in trial NCT06988709?

The interventions under investigation include: Real-time Visual Feedback (OTHER), Real-time Auditory Feedback (OTHER), Real-time Verbal Feedback (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06988709?

This trial is sponsored by Keller Army Community Hospital, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06988709 being conducted?

This trial has 1 study location across New York. 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