Femur
Conditions
Interventions
Enrolled participants will be randomized using computer software, stratified by age and sex (15 participants per group), by an individual unrelated to the study data collection and analysis. The activ
2) unipodal support, 5 seconds on each member, alternating, during 10 repetitions, 2 times, with 30 seconds of interval in between
3) step up, performed on a mini-ladder, 10 repetitions on each limb, 3 sets, with 30 seconds of rest between sets
4) sitting abduction, resisted by an elastic band, 12 movements, 3 series, with a rest of 30 seconds
5) hip raise, 10 movements, 3 sets, with 30 seconds of rest between sets
6) light walking until completing 20 minutes of training.
Transcranial direct current electrical stimulation will be applied concomitantly with the exercise, as recommended for painful pathologies and
I03.350
E02.331.750
Sponsors
Universidade Estadual de Campinas
Universidade Estadual de Campinas
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Voluntaries with greater trochanteric pain syndrome; older than 18 years old; from both genders
Exclusion criteria
Exclusion criteria: Motor or cardiovascular impairment precluding physical exercise; uncontrolled epilepsy; extensive skin lesions
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| An improvement in hip pain is expected on the 30th day, measured by the Brazilian version of the scale Victorian Institute for Sport Assessment for Gluteal Tendinopathy, with the active group statistically superior to the control group. | — |
Secondary
| Measure | Time frame |
|---|---|
| A larger improvement of the active group is expected immediately after the protocol and on the 60th day, measured by the Brazilian version of the scale Victorian Institute for Sport Assessment for Gluteal Tendinopathy.;A larger improvement of the active group is expected immediately after the protocol, on the 30th day, and on the 60th day, in various domains of the Brazilian version of the Copenhagen Hip and Groin Outcome Score.;A larger improvement of the active group is expected in various pain subtypes immediately after the protocol, on the 30th day, and on the 60th day, measured by the Brazilian version of the Pain Quality Assessment Scale.;A larger improvement of the active group in the pain felt in palpation of the greater trochanter immediately after the protocol, on the 30th day, and on the 60th day, measured by visual analogue scale.;A larger improvement of the maximum time in unipedal support of the active group immediately after the protocol, on the 30th day and on the 60th day. | — |
Countries
Brazil
Contacts
Public ContactJean De Souza
Universidade Estadual de Campinas
Outcome results
None listed