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Effect of physiotherapeutical treatment on hip pain in women

Randomized clinical trial: The effect of a physiotherapy protocol in Greater trochanteric pain syndrome in women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-84zdp6
Enrollment
Unknown
Registered
2018-05-15
Start date
2018-07-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Trochanteric bursitis. Gluteal tendinitis.

Interventions

The physiotherapeutic protocol will have 15 participants, who will perform exercises of myofascial release, resistance, strengthening and motor control, stabilizing muscles of the trunk and hip, which
Other

Sponsors

Universidade Estadual Paulista, Faculdade de Filosofia e Ciências
Lead Sponsor
Universidade Estadual Paulista, Instituto de Biociências
Collaborator

Eligibility

Sex/Gender
Female
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: Clinical diagnosis of major trochanter pain syndrome, chronic lateral pain in the hip greater than or equal to 3 months, presenting pain (4/10) in the visual analogue scale, tenderness in the trochanter region (4/10), pain during daily activities, pain in at least 1 of the 7 provocative clinical tests of pain, which is intended to transmit compressive or tension forces in the tendons of the abductor gluteal muscles. To present age and gender comparable to the intervention group

Exclusion criteria

Exclusion criteria: Presenting a body mass index more than 36 kg / m2, received some type of invasive intervention to reduce pain in the region evaluated in the last year, physiotherapeutic intervention in the last three months, present any limitation in the range of motion of the regions of the column, hip or MMII that disables gait or testing, any disease that affects the neuromuscular system or that may prevent collection, surgery on the spine or hip, any infectious condition, any neoplasia or can not commit to the weeks of treatment

Design outcomes

Primary

MeasureTime frame
Increase in the strength of the gluteus medium, gluteus maximus and tensor fascia latae of the intervention group, evaluated by means of the dynamometer, from the variation of at least 10% between the evaluations;Pain reduction after intervention group training of at least 10% in the intragroup analysis

Secondary

MeasureTime frame
Increased electromyographic activity of the gluteus medium, gluteus maximus and tensor fascia latae muscles during gait at the preferred speed, in the intervention group;Decreased electromyographic activity of the internal oblique, external oblique, rectus abdominus and multifidus muscles during gait, at the preferred speed, in the intervention group

Countries

Brazil

Contacts

Public ContactGuilherme;Marcelo Nava;Navega

Universidade Estadual Paulista, Faculdade de Filosofia e Ciências;Universidade Estadual Paulista, Faculdade de Filosofia e Ciências

gtanava@gmail.com;navega@marilia.unesp.br+5501434021300;+5501434021300

Outcome results

None listed

Source: REBEC (via WHO ICTRP)