- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01491048
Evaluation of Functional Rehabilitation in Patients Undergoing Physiotherapy After Total Hip Arthroplasty (Artrhosis)
Evaluation of Functional Rehabilitation Therapy in Patients Undergoing Physiotherapy After Total Hip Arthroplasty
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The Total Hip Arthroplasty (THA) is a surgical procedure which has been used for more than half a century in the treatment of hip joint diseases.
The Physiotherapy is an important component in the care of patients undergoing THA.
In order to reduce the length of hospitalization after THA, to promote functional independence and to monitor clinical events during hospitalization and up to the 30th postoperative day, the Hip Surgery Group (HSG) of the Department of Orthopedics and Traumatology Department of Orthopedics and Traumatology of Hospital de Clinicas de Porto Alegre (HCPA) has developed a global, multidisciplinary Assistance Protocol of the HSG with outpatient consultations and scheduled home visits for patients that have undergone THA at HCPA.
The team which developed the Assistance Protocol of the HSG consists of orthopedic doctors and anesthesiologists, nurses and social workers.
The insertion of the Physiotherapist in the THA Assistance Protocol is of great importance owing to the professional skills of that professional in the areas of prevention and rehabilitation, working with the multidisciplinary team in functional evaluation and in physical therapy of patients that underwent THA.
The monitoring of the physiotherapist is essential to establish a functional diagnosis, aiming pain relief, promoting the early functional rehabilitation, the reintegration of the patients in their daily activities and offering a better quality of life through reintegration into social life.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
RS
-
Porto Alegre, RS, Brazil, 90035-903
- Hospital de Clínicas de Porto Alegre
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Patients with indication for THA.
Exclusion Criteria:
- Patients who refuse to participate in this study.
- Patients who live outside the city of Porto Alegre, due to difficulties for visits and the protocol monitoring.
- Patients with femoral neck fracture, due to the impossibility of evaluation.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: THA Physiotherapy
Physiotherapy care during the period of hospitalization after THA.
|
Patients will be randomized into two groups.
The control group will receive care from the team of the THA Assistance Protocol already used by the HSG of HCPA without the intervention of physiotherapy.
During hospitalization, the group of cases will be submitted to physical therapy associated with the intervention of the team of the THA Assistance Protocol.
Other Names:
No physiotherapy after THA
Other Names:
|
|
Active Comparator: No physiotherapy after THA
No Physiotherapy care during the period of hospitalization after THA.
|
No physiotherapy after THA
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Physiotherapeutic Rehabilitation after THA.
Time Frame: 15 days after discharge
|
Patients hospitalized in the HCPA for THA surgery, are submitted to an assessment and are randomized.
Soon after, the treatment group receives the physiotherapy protocol while the control group receives guidance together with the THA Assistance Protocol.
Fifteen days later the patients return to hospital where they are reassessed.
|
15 days after discharge
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Physiotherapeutic Rehabilitation after THA.
Time Frame: 15 days after discharge.
|
Patients will be evaluated through tests of strength, range of motion, limb discrepancy, hip functionality and quality of life before and after discharge.
|
15 days after discharge.
|
Collaborators and Investigators
Investigators
- Principal Investigator: Carolina S Umpierres, Bachelor, Hospital de Clínicas de Porto Alegre
Publications and helpful links
General Publications
- Walker RL, Fromm PO. Metabolism of iron by normal and iron deficient rainbow trout. Comp Biochem Physiol A Comp Physiol. 1976;55(4A):311-8. doi: 10.1016/0300-9629(76)90052-9. No abstract available.
- Umpierres CS, Ribeiro TA, Marchisio AE, Galvao L, Borges IN, Macedo CA, Galia CR. Rehabilitation following total hip arthroplasty evaluation over short follow-up time: randomized clinical trial. J Rehabil Res Dev. 2014;51(10):1567-78. doi: 10.1682/JRRD.2014.05.0132.
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Joint Diseases
- Musculoskeletal Diseases
- Rheumatic Diseases
- Arthritis
- Osteoarthritis
- Osteoarthritis, Hip
- Physiological Effects of Drugs
- Neurotransmitter Agents
- Molecular Mechanisms of Pharmacological Action
- Autonomic Agents
- Peripheral Nervous System Agents
- Cholinergic Agents
- Enzyme Inhibitors
- Nootropic Agents
- Cholinesterase Inhibitors
- Parasympathomimetics
- Tacrine
Other Study ID Numbers
- 09242
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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