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Using Real Time Biofeedback to Alter Running Mechanics

K

Keller Army Community Hospital

Status

Completed

Conditions

Healthy

Treatments

Device: Biofeedback Sensor

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

NCT02495792
404239-2

Details and patient eligibility

About

The purposes of this study are 1) to assess foot strike patterns initially, at six months and at one year between two groups of runners attempting to transition to a non-rearfoot strike pattern (NRFS) with and without the use of biofeedback technology, and 2) to prospectively compare injury incidence rates at one year between NRFS and rearfoot strike (RFS) runners.

Enrollment

191 patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Between the age of 18 - 50 years
  2. Run on average 12mi per week
  3. DOD beneficiaries who intend to remain at West Point, NY for the next 12 months at time of study enrollment
  4. Read and speak English well enough to provide informed consent and follow study instructions

Exclusion criteria

  1. Known pregnancy currently or in the previous 6 months
  2. Lower extremity or low back pain in the previous 3 months
  3. Lower extremity or low back surgery in the previous 6 months
  4. Any lower extremity or low back exercise limiting profile
  5. Previous stress fracture of the foot
  6. Participant who has a non-rearfoot strike running pattern

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

191 participants in 2 patient groups

Control group
No Intervention group
Description:
Group does not receive the biofeedback sensor
Biofeedback group
Experimental group
Description:
Group does receive the biofeedback sensor
Treatment:
Device: Biofeedback Sensor

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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