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Physiotherapeutic treatment in people who underwent hip replacement surgery

Comparison between two physiotherapeutic rehabilitation methods in individuals submitted to total hip arthroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3chymm
Enrollment
Unknown
Registered
2018-07-12
Start date
2016-09-30
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

osteoarthritis

Interventions

Participants will be allocated in one of the groups (conventional physiotherapy - GFC, or conventional physiotherapy group associated with proprioceptive exercises - GP) as the entry order in the stud
SANDERS, 2003)), and performed in the sitting position and in the supine position with the aid of leggings and elastic bands. Later, if patients are able to perform movements without pain, isometrics
COSTILL
Kenney, 2010
Kisner
COLBY, 2005). They will be performed in the sitting position, supine and standing position, and the resistance imposed by leggings. Initially the load used will correspond to the range of 10 to 20% of
COLBY, 2005). When patients reach maximum strength by manual test Kendall (Kendall, McCreary, Provance, 2007) load will used for approximately 45-50% of repetition maximum (1RM) (Campos et al., 2002).
Earle 2008) and allows for the calculation of
Other
G11.427.410.698.277

Sponsors

Universidade Federal de Mato Grosso do Sul
Lead Sponsor
Universidade Federal de Mato Grosso do Sul
Collaborator
Centro Ortopédico Municipal (CENORT)
Collaborator

Eligibility

Age
50 Years to 90 Years

Inclusion criteria

Inclusion criteria: Age between 50 and 90 years; performed ATQ due to OA; four to five weeks postoperatively; who are not enrolled or participating in another physiotherapeutic treatment program; reside in Campo Grande or region.

Exclusion criteria

Exclusion criteria: History of stroke; Parkinson's disease; gait disturbances of neurological origin; clinical depression or disease that compromises the level of cognition; revisions of CKD, postoperative complications such as infection or dislocation; cardiopulmonary contraindications to perform physical exercise.

Design outcomes

Primary

MeasureTime frame
Muscle activation of the gluteus medius The activation of the gluteus medius of the operated and non-operated limb will be evaluated by means of surface electromyography. For the study, an electromyograph of the Miotec brand (Miotec Equipamentos biomédicos LTDA, Porto Alegre, RS, Brazil), calibrated with 1000-fold gain, 10Hz high-pass filter, 500Hz low-pass filter and 60 notch filter Hz. The sampling frequency used shall be 2000 Hz. The electrodes shall be positioned bilaterally at 50% of the antero-superior iliac spine line to the greater trochanter, 3 cm apart, and the reference electrode shall be positioned over the process of the ulna (SENIAM, 2017). Data regarding the median frequency, neuromuscular efficiency (NME) and the index of activation of the gluteus medius muscle will be collected, and in this study the mean value of the root mean square (RMS) will be used. In what will be considered significant results, those that obtained increased efficiency and activation of the gluteus medius in the study period (6 weeks), verified by means of the test of analysis of two-way variance from the finding of a variation of at least 5% in pre and post-intervention measurements.

Secondary

MeasureTime frame
Secondary outcomes are not expected

Countries

Brazil

Contacts

Public ContactMariana Budib

Universidade Federal de Mato Grosso do Sul

marianabudib@gmail.com+55(67)981042396

Outcome results

None listed

Source: REBEC (via WHO ICTRP)