Effect of Strength and Coordination Training on Biomechanics and Injury in New Runners

June 17, 2019 updated by: Virginia Commonwealth University
The investigators hypothesize that new runners participating in an 8 week strength and coordination training program prior to beginning to run will 1) display different coordination patterns , and 2) experience fewer injuries, compared to new runners who do not perform strength or coordination training prior to running.

Study Overview

Detailed Description

The study will investigate the effect of a sequenced training program - beginning with strength training, followed by running-specific coordination exercises, and finally a gradual introduction to running - on strength, coordination and injury incidence in a group of novice runners. he investigators hypothesize that runners who perform strength and coordination training prior to beginning to run will 1) demonstrate greater lower extremity strength, 2) demonstrate alters coordination patterns and 3) experience fewer injuries, when compared to a control group of novice runners who perform no physical preparation prior to a gradual introduction to running. The possible long-term benefits of this study include reduced burden of running-related injuries, increased participation in the sport of running, improved cardiovascular and metabolic health characteristics, and reduced incidence of disease such as cardiovascular events and cancer.

Study Type

Interventional

Enrollment (Actual)

70

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Virginia
      • Richmond, Virginia, United States, 23298
        • Virginia Commonwealth University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 60 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • No previous participation in running races
  • Run less than 10km total in past year
  • Able to run continuously (ie at least 5mph) for 5 min (so that biomechanical analysis of running form can be conducted)
  • Female participants may not be pregnant
  • Participants will be screened using the PARQ+ form, and Parmed-X form completed by a physician if necessary
  • Cleared for physical activity through screening
  • English-speaking

Exclusion Criteria:

  • Previous (at any time of life) training of 3 or months of consistently running 3 or more days per week

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: PREVENTION
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Strength and Coordination Training
The strength and coordination group will perform a progression of exercises utilizing body weight and resistance bands as resistance. Exercises include squats, lunges, jumps etc. typical of a normal strength training program.
Perform training exercises 3/week. Weeks 1-2: general strength (isolated muscle groups) Weeks 3-4: running-specific strength (multi-joint, upright) Weeks 5-6: power/coordination I (low amplitude/intensity) Weeks 7-8: power/coordination II (higher amplitude/intensity) Weeks 9-16: Run training. Each training session will start with a 10 minute strength & coordination warm up. Group will gradually progress from mixed run/walk for 20 minutes to a 40 minute run.
ACTIVE_COMPARATOR: Walking
The walking group will be instructed to walk 3x/week, progressing from 30 to 45 min over 8 weeks.
Perform training exercises 3/week. Weeks 1-2: 30 minute walk Weeks 3-4: 35 minute walk Weeks 5-6: 40 minute walk Weeks 7-8: 45 minute walk Weeks 9-16: Run training. Each training session will start with a 10 minute walking warm up. Group will gradually progress from mixed run/walk for 20 minutes to a 40 minute run.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Running biomechanics
Time Frame: Change from week 0 to week 16
Relative joint motions will be assessed continuously throughout the stride cycle using a vector coding technique.
Change from week 0 to week 16

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Running injury.
Time Frame: Measured in days over the 16 week training period.
Time to first running related injury.
Measured in days over the 16 week training period.

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Running performance
Time Frame: 16 weeks
5km time trial at the end of 16 weeks training.
16 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Sheryl Finucane, PT, PhD, CEEAA, Virginia Commonwealth University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

January 15, 2017

Primary Completion (ACTUAL)

June 4, 2018

Study Completion (ACTUAL)

June 4, 2018

Study Registration Dates

First Submitted

September 15, 2017

First Submitted That Met QC Criteria

September 19, 2017

First Posted (ACTUAL)

September 26, 2017

Study Record Updates

Last Update Posted (ACTUAL)

June 18, 2019

Last Update Submitted That Met QC Criteria

June 17, 2019

Last Verified

June 1, 2019

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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