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Footwear Minimalism Study

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ClinicalTrials.gov Identifier: NCT01334346
Recruitment Status : Completed
First Posted : April 13, 2011
Last Update Posted : March 29, 2013
Information provided by (Responsible Party):
University of British Columbia

Brief Summary:

The following study proposes to investigate the injury risk associated with the use of a new category of running footwear: the minimalist shoe. A group of experienced adult male and female runners with neutral foot types will take part in this study. All participants will be randomized to receive one of three different shoes: a full minimalist shoe (Vibram 5-Fingers), a partial minimalist shoe (Nike Free 3.0) and a conventional neutral supportive running shoe (Nike Pegasus), while training for a 10k event over a 14-week period. Outcomes to be investigated are pain, footwear perception, and number of injury events.

The hypothesizes is that participants using the minimalist footwear during their running program will experience a reduction in running related pain. A greater degree of footwear minimalism will result in a greater reduction in pain (compared to the partial minimalist shoe, Nike Free).

Condition or disease Intervention/treatment Phase
Healthy Runners Other: Nike Pegasus Other: Nike Free 3.0 Other: Vibram Five Fingers Shoe Phase 2

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 91 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: An Investigation on Footwear Minimalism and Injury Risk in Runners
Study Start Date : August 2011
Actual Primary Completion Date : July 2012
Actual Study Completion Date : July 2012

Arm Intervention/treatment
Active Comparator: Neutral Shoe
Conventional, non-minimalist, footwear.
Other: Nike Pegasus
Conventional neutral supportive running footwear. Non minimalist.

Experimental: Partial minimalist shoe Other: Nike Free 3.0
Partial minimalist shoe with partially elevated heel, but with increased mid-sole flexibility.

Experimental: Full minimalist Other: Vibram Five Fingers Shoe
Full minimalist shoe. Virtually no mid-sole, therefore no heel elevation or forefoot rockering. A proxy for a barefoot running condition.

Primary Outcome Measures :
  1. Number of Injury Events [ Time Frame: 12 weeks ]
    Number of run injury events (defined as unable to complete 3 consecutive running workouts due to running related pain). A calculation of injury incidence will be based on this number after dividing by the number of athletic exposures.

Secondary Outcome Measures :
  1. Foot and Ankle Disability Index (FADI) [ Time Frame: Week 12 ]
  2. Numerical Pain Scale (NPS) for Overall Running Related Pain [ Time Frame: Week 12 ]
  3. Regional Specific NPS: Shin and Calf Pain [ Time Frame: Week 12 ]
  4. Regional Specific NPS: Foot and Ankle Pain [ Time Frame: 12 Week ]
  5. Regional Specific NPS: Knee Pain [ Time Frame: 12 Weeks ]
  6. Regional Specific NPS: Pelvis and Groin Pain [ Time Frame: 12 Week ]
  7. Regional Specific NPS: Lower Back Pain [ Time Frame: 12 Week ]

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 50 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Minimum of 5 years experience running
  • Have been running on a regular basis (minimum once per week) over the past 6 months
  • Able to run for 60 minutes continuously
  • Can tolerate 20-40km per week in training
  • Neutral foot posture according to the Foot Posture Index.

Exclusion Criteria:

  • Have not experienced a running related injury requiring a stoppage of 2-weeks or more in the past 6 months
  • History of surgery to their plantar fascia or Achilles tendon
  • Have already been running in a minimalist shoe
  • Have a diagnosis of osteoarthritis - or other degenerative musculoskeletal disorder - affecting the lower extremity
  • Are currently taking analgesic medication.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01334346

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Canada, British Columbia
University of British Columbia
Vancouver, British Columbia, Canada, V6T 1Z3
Sponsors and Collaborators
University of British Columbia
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Principal Investigator: Jack Taunton, MD University of British Columbia
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Responsible Party: University of British Columbia
ClinicalTrials.gov Identifier: NCT01334346    
Other Study ID Numbers: H11-00931
First Posted: April 13, 2011    Key Record Dates
Last Update Posted: March 29, 2013
Last Verified: March 2013
Keywords provided by University of British Columbia:
Injury incidence
injury risk