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

Primary Purpose

Injuries, Patellofemoral Pain Syndrome, Iliotibial Band Syndrome

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Strength and Coordination Training
Walking
Sponsored by
Virginia Commonwealth University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Injuries focused on measuring running related injuries

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Virginia Commonwealth University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Strength and Coordination Training

Walking

Arm Description

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.

The walking group will be instructed to walk 3x/week, progressing from 30 to 45 min over 8 weeks.

Outcomes

Primary Outcome Measures

Running biomechanics
Relative joint motions will be assessed continuously throughout the stride cycle using a vector coding technique.

Secondary Outcome Measures

Running injury.
Time to first running related injury.

Full Information

First Posted
September 15, 2017
Last Updated
June 17, 2019
Sponsor
Virginia Commonwealth University
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1. Study Identification

Unique Protocol Identification Number
NCT03293121
Brief Title
Effect of Strength and Coordination Training on Biomechanics and Injury in New Runners
Official Title
Effect of Strength and Coordination Training on Biomechanics and Injury in New Runners
Study Type
Interventional

2. Study Status

Record Verification Date
June 2019
Overall Recruitment Status
Completed
Study Start Date
January 15, 2017 (Actual)
Primary Completion Date
June 4, 2018 (Actual)
Study Completion Date
June 4, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Virginia Commonwealth University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Injuries, Patellofemoral Pain Syndrome, Iliotibial Band Syndrome
Keywords
running related injuries

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
70 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Strength and Coordination Training
Arm Type
Experimental
Arm Description
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.
Arm Title
Walking
Arm Type
Active Comparator
Arm Description
The walking group will be instructed to walk 3x/week, progressing from 30 to 45 min over 8 weeks.
Intervention Type
Behavioral
Intervention Name(s)
Strength and Coordination Training
Intervention Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Walking
Intervention Description
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.
Primary Outcome Measure Information:
Title
Running biomechanics
Description
Relative joint motions will be assessed continuously throughout the stride cycle using a vector coding technique.
Time Frame
Change from week 0 to week 16
Secondary Outcome Measure Information:
Title
Running injury.
Description
Time to first running related injury.
Time Frame
Measured in days over the 16 week training period.
Other Pre-specified Outcome Measures:
Title
Running performance
Description
5km time trial at the end of 16 weeks training.
Time Frame
16 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sheryl Finucane, PT, PhD, CEEAA
Organizational Affiliation
Virginia Commonwealth University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Virginia Commonwealth University
City
Richmond
State/Province
Virginia
ZIP/Postal Code
23298
Country
United States

12. IPD Sharing Statement

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

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