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NCT Number: NCT06988709

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 baseline running and each retraining technique.

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Key information

Conditions

Age range

17 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Keller Army Community Hospital

West Point, New York, 10996, United States

Location status: Recruiting

Location contact

Kenneth L Cameron, PhD

CONTACT

[email protected]

About this study

The purpose of our study is to establish the most effective running retraining technique to decrease ground contact time utilizing three common running retraining methods in healthy runners.

The first aim will be to apply three running retraining conditions and assess the change in ground contact time and other spatiotemporal and biomechanical variables between the runner's baseline running and each retraining condition.

The three running conditions will be at the participant's self-selected speed corresponding to "a comfortable run for 30 minutes". The conditions will be, condition 1: a verbal cue to "pull your foot off the ground as quickly as you can," condition 2: a metronome set to 10% above their preferred cadence found during the baseline run, and condition 3: visual feedback to reduce their ground contact time through observing that number in real time provided by a commercial IMU. The participant will attempt to lower that to 5% below their baseline run ground contact time by being given that target number on a sheet of paper.

The second aim will be to examine the effect of the 3 running conditions on the runner's level of exertion and difficulty using the Omni Rate of Perceived Exertional Scale, the Rate of Perceived Difficulty, and ranking the techniques from 1 to 3 on which they felt was most natural.

We hypothesize that each method will reduce ground contact time, but condition 3 providing continuous visual feedback will result in the most consistent decrease to ground contact time across the runners and will be perceived as the easiest to perform.

Overall, this study will provide clinicians with a running retraining intervention that has been objectively shown to decrease ground contact time and provide researchers with a method to further investigate its effect on running injuries.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Military Service Member or USMA cadet between the ages of 17-60
  • Run at least 2 miles three times per week for the past 3 months
  • Able to run for at least 15 continuous minutes at a self-selected speed
  • Fluent in the English language to read and provide informed consent and follow study instructions

Exclusion criteria

  • Lower extremity or low back pain in the previous 3 months
  • Lower extremity or low back surgery in the previous 6 months
  • Self-reported pregnancy or given birth within the last 6 months
  • Currently on a profile that restricts or limits running

Treatment and study plan

Real-time Visual Feedback

Other

Runners will visualize their real-time ground contact time (GCT) measured by the RunScribe on a TV screen. They will be instructed to run with a goal of matching their target GCT. Their target GCT will be 5% less than their baseline.

Real-time Auditory Feedback

Other

Runners will be instructed to match their step rate to a target step rate, 10% above their baseline step rate. A metronome will be played over a speaker to provide real-time auditory feedback of the target step rate.

Real-time Verbal Feedback

Other

The clinician will provide real-time verbal feedback to runner to "pull your foot off the ground as quickly as you can," every 15 seconds during the retraining condition.

Primary outcomes

  1. Ground Contact Time

    Time frame: Within a single session, measured pre-intervention (baseline) and during each running condition intervention

    The amount of time in milliseconds that the foot remains in contact with the ground while running. GCT will be measured through the RunScribe device.

Secondary outcomes

  1. Step Rate

    Time frame: Within a single session, measured pre-intervention (baseline) and during each running condition intervention

    Number of steps per minute that the participant takes in one minute while running.

  2. Average Vertical Loading Rate (AVLR)

    Time frame: Within a single session, measured pre-intervention (baseline) and during each running condition intervention

    Measured in Bodyweights/second. Total interval considered for loading rate is the start of stance phase through the impact peak location. We will calculate the average loading rate from 20% of the impact peak value to 80% of the impact peak magnitude.

  3. Braking Impulse

    Time frame: Within a single session, measured pre-intervention (baseline) and during each running condition intervention

    Kg*m/s. The impulse associated with the deceleration while running.

  4. Step Length

    Time frame: Within a single session, measured pre-intervention (baseline) and during each running condition intervention

    The distance measured in centimeters while running from one foot strike to the next foot strike.

Study contacts

Contact information is provided by the study sponsor or research team.

Jamie Morris, DPT, DSc

CONTACT

[email protected]

315-774-8350

Jennah Bulen, DPT

CONTACT

[email protected]

315-774-8350

Sponsors and collaborators

Lead sponsor

Keller Army Community Hospital

Fed

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
May 25, 2025
Registry last updated
Dec 12, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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