- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03293121
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
Status
Completed
Intervention / Treatment
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.
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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.
Sponsor
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- HM20010685
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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