Barefoot Running Clinical Trial
Official title:
16 Weeks of Progressive Barefoot Running Training Changes Impact Force and Muscle Activation in Habitual Shod Runners
| Verified date | June 2016 |
| Source | University of Sao Paulo |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | Brazil: Ethics Committee |
| Study type | Observational |
The purpose of this study was to evaluate the influence of 16 weeks of progressive barefoot running training on impact force and muscle activation in habitual shod runners. Habitual shod runners were tested barefoot (BF) and shod (SH), before and after 16 weeks of progressive barefoot running training. Tests consisted of running on instrumented treadmill at 9 km/h, for 10 minutes in each experimental condition. Nine data acquisitions (10 s) of vertical ground reaction force (VGRF) and electromyographic (EMG) signal were conducted in each experimental condition, for each test.
| Status | Completed |
| Enrollment | 6 |
| Est. completion date | May 2013 |
| Est. primary completion date | March 2013 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Both |
| Age group | 18 Years to 40 Years |
| Eligibility |
Inclusion Criteria: - to have a minimum of 6 months of regular running training; - to have a minimum of 6 months of experience in running on treadmills; - do not have suffered any orthopedic injury in the last 12 months. Exclusion Criteria: - to have experience in minimalist/barefoot running; - to be habitual forefoot striker; - to complete less than 80% of training; - to suffer any injury during training. |
Observational Model: Cohort, Time Perspective: Prospective
| Country | Name | City | State |
|---|---|---|---|
| Brazil | Ana Paula da Silva Azevedo | São Paulo | SP |
| Lead Sponsor | Collaborator |
|---|---|
| University of Sao Paulo |
Brazil,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Parameters of the vertical component of Ground Reaction Force (VGRF) related to impact force | Biomechanical parameters related to impact forces, as magnitude of VGRF's first peak, time to reach first peak of VGRF and implulse from the first 50 ms, will be measured. | 4 months | Yes |
| Primary | Electromyographic (EMG) parameters related to muscle activation intensity | EMG signal will be measeured and the RMS, a parameter that reflects muscle activation intensity, will be evaluated. | 4 months | Yes |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
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