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CompletedNCT03293121Updated Jun 18, 2019

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

An interventional study of Strength and Coordination Training and Walking in Injuries, Patellofemoral Pain Syndrome and Iliotibial Band Syndrome, sponsored by Virginia Commonwealth University. Completed at 1 site in United States. Open to participants aged 18 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-06-18.

Primary conditionIliotibial Band SyndromeRegistry: Wounds and InjuriesReclassifiedWhy we changed it
Registry
Wounds and Injuries — the first condition term the registry derived for this study.
ClinicalTrials.gg
Iliotibial Band Syndrome
Why
  1. The study's listed conditions name Iliotibial Band Syndrome, a narrower term within Wounds and Injuries.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Virginia Commonwealth University · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 8 months after the study started (first participant enrolled Jan 2017, registered Sep 2017).

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Phase
Not applicable
Study type
Interventional
Enrollment
70
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Injuries
  • Patellofemoral Pain Syndrome
  • Iliotibial Band Syndrome

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Keywords

  • running related injuries
03

In context

Iliotibial Band Syndrome Reclassified

19 studies on the registry are indexed under Iliotibial Band Syndrome; 7 are open to participants now.

This study's enrollment of 70 is above the median of 40 across 18 interventional studies indexed under Iliotibial Band Syndrome.

Browse Iliotibial Band Syndrome studies →

Lead sponsor

Virginia Commonwealth University is the lead sponsor of 648 studies on the registry; 80 are open to participants now.

Of its 90 completed or terminated interventional studies of FDA-regulated products, 64 (71%) have results posted.

Compared within Iliotibial Band Syndrome, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Wounds and Injuries. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

  • Previous (at any time of life) training of 3 or months of consistently running 3 or more days per week
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
70 participants (actual)

Study arms

  • 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.

    Behavioral: Strength and Coordination Training

  • Active comparator
    Walking

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

    Behavioral: Walking

Interventions

  • BehavioralStrength and Coordination Training

    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.

  • BehavioralWalking

    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.

06

What researchers measure

Primary outcomes

  1. Running biomechanics

    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 outcomes

  1. Running injury.

    Time to first running related injury.

    Time frame: Measured in days over the 16 week training period.

Other outcomes

  1. Running performance

    5km time trial at the end of 16 weeks training.

    Time frame: 16 weeks

07

Study locations

1 site
  • Virginia Commonwealth University
    Richmond, Virginia 23298, United States
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Jan 2017 to primary completion in Jun 2018, 16 months.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 15, 2017
First posted
Sep 26, 2017
StartActual
Jan 15, 2017
Primary completionActual
Jun 4, 2018
CompletionActual
Jun 4, 2018
Last update
Jun 18, 2019
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 18, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03293121
Responsible party
Sponsor
First posted
Sep 26, 2017
Start date
Jan 15, 2017
Primary completion
Jun 4, 2018
Completion
Jun 4, 2018
Last update
Jun 18, 2019

Study contacts

Sheryl Finucane, PT, PhD, CEEAA
principal investigator · Virginia Commonwealth University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jun 2019. You cannot join it, but the record below documents what was studied.

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