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

Virginia Commonwealth University (VCU) logo

Virginia Commonwealth University (VCU)

Status

Completed

Conditions

Injuries
Iliotibial Band Syndrome
Patellofemoral Pain Syndrome

Treatments

Behavioral: Walking
Behavioral: Strength and Coordination Training

Study type

Interventional

Funder types

Other

Identifiers

NCT03293121
HM20010685

Details and patient eligibility

About

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.

Full 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.

Enrollment

70 patients

Sex

All

Ages

18 to 60 years old

Volunteers

Accepts 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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

70 participants in 2 patient groups

Strength and Coordination Training
Experimental group
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.
Treatment:
Behavioral: Strength and Coordination Training
Walking
Active Comparator group
Description:
The walking group will be instructed to walk 3x/week, progressing from 30 to 45 min over 8 weeks.
Treatment:
Behavioral: Walking

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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