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Step Rate in Recreational Runners

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Mayo Clinic

Status

Completed

Conditions

Gait Disorder, Sensorimotor

Treatments

Behavioral: Change in running cadence

Study type

Interventional

Funder types

Other

Identifiers

NCT03057522
16-008532

Details and patient eligibility

About

This will be a pilot study to determine if a 6 week home training program can increase preferred step rate (cadence) in recreational runners. Increase in step rate has been correlated with decreased stress at lower limb joints in runners. This has the potential of decreasing overuse injuries in this population.

Research participants will have their preferred cadence evaluated at the beginning of the study. The athletes will be randomly assigned to two groups. One group will continue to train without intervention and the other group will train at a cadence of 10% higher than their preferred step rate.

At the end of 6 weeks the participants will have their preferred cadence reevaluated using the same method as pre-participation cadence was determined.

The investigators hypothesis the preferred running cadence of recreational runners following the intervention will be 5-10% greater than prior to the intervention and the increased cadence will be maintained for 6 months following the intervention.

Enrollment

38 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • healthy male or female runners
  • 18 years of age or greater
  • run two or more times per week most weeks of the year for at least 4 years
  • cadence of 85 strides/min or less as determined at initial evaluation
  • no musculoskeletal injuries or illnesses that would limit running in the last 6 months
  • currently running at least 15 miles a week

Exclusion criteria

  • baseline running cadence greater than 85 strides/min
  • inability to run
  • cardiovascular disease
  • greater than 2 cardiovascular risk factors
  • peripheral vascular disease
  • neurological disease
  • musculoskeletal injury or disease that causes pain with running

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

38 participants in 2 patient groups

Intervention Group
Experimental group
Description:
This group will undergo home exercise program designed to increase their running cadence.
Treatment:
Behavioral: Change in running cadence
Control Group
No Intervention group
Description:
This group will not receive any intervention.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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