NCT03057522

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
38

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2017

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2017

Completed
13 days until next milestone

First Submitted

Initial submission to the registry

February 14, 2017

Completed
6 days until next milestone

First Posted

Study publicly available on registry

February 20, 2017

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2018

Completed
Last Updated

November 14, 2018

Status Verified

November 1, 2018

Enrollment Period

1.3 years

First QC Date

February 14, 2017

Last Update Submit

November 9, 2018

Conditions

Keywords

RunCadenceHome exercise

Outcome Measures

Primary Outcomes (2)

  • Running cadence

    Running cadence (steps per minute) will be evaluated using a running cadence sensor to determine if the intervention subjects increased their running cadence by 10 steps per minute following the intervention.

    6 weeks

  • Running cadence

    Running cadence (steps per minute) will be evaluated using a running cadence sensor to determine if the intervention subjects maintained their increased running cadence for 6 months following the intervention.

    6 months

Study Arms (2)

Intervention Group

EXPERIMENTAL

This group will undergo home exercise program designed to increase their running cadence.

Behavioral: Change in running cadence

Control Group

NO INTERVENTION

This group will not receive any intervention.

Interventions

The intervention will involve a home exercise program designed to increase the running cadence in recreational runners.

Intervention Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • healthy male or female runners
  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Mayo Clinic in Rochester

Rochester, Minnesota, 55905, United States

Location

MeSH Terms

Conditions

Gait Disorders, Neurologic

Condition Hierarchy (Ancestors)

Neurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Jonathan T Finnoff

    Mayo Clinic

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Prospective, randomized, controlled study evaluating whether a home exercise program can increase the running cadence of recreational runners.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor of Physical Medicine and Rehabilitation

Study Record Dates

First Submitted

February 14, 2017

First Posted

February 20, 2017

Study Start

February 1, 2017

Primary Completion

June 1, 2018

Study Completion

June 1, 2018

Last Updated

November 14, 2018

Record last verified: 2018-11

Data Sharing

IPD Sharing
Will not share

No IPD will be shared with other researchers

Locations