The Impact of Two Different Physical Therapy Programs in the Rehabilitation of Patients Undergoing Anterior Approach Hip Replacement Surgery
NCT ID: NCT04492462
Last Updated: 2021-09-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
200 participants
INTERVENTIONAL
2019-10-22
2023-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Formal Physical Therapy
Formal Physical Therapy
Patients will undergo standard physical therapy following their surgery with a physical therapist in an office
Self-directed Physical Therapy
Self-directed Physical Therapy
Patients will undergo self-directed physical therapy in the comfort of their own home by completing a list of exercises and stretches without the direct supervision of a physical therapist in a physical therapist office
Interventions
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Formal Physical Therapy
Patients will undergo standard physical therapy following their surgery with a physical therapist in an office
Self-directed Physical Therapy
Patients will undergo self-directed physical therapy in the comfort of their own home by completing a list of exercises and stretches without the direct supervision of a physical therapist in a physical therapist office
Eligibility Criteria
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Inclusion Criteria
* Patients undergoing primary anterior total hip arthroplasty for the diagnosis of osteoarthritis
* Patients with no previous invasive hip surgery (such as a previous hip replacement)
Exclusion Criteria
* Patients with a recent history (\<1 year) of heart attack, stroke, and lung clots.
* Previous invasive surgery on the hip undergoing replacement
* Patients with dementia, Parkinson's, or other neurological disorders
* Non-ambulatory patients
* Patients with impaired ability to consent, whether because of mental illness or otherwise
* Patients being discharged to a rehabilitation center
* Patients that experience intra-operative complications
18 Years
80 Years
ALL
Yes
Sponsors
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Rutgers, The State University of New Jersey
OTHER
Responsible Party
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Stephen Kayiaros MD
Principal Investigator, Clinical Assistant Professor
Principal Investigators
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Stephen T Kayiaros, MD
Role: PRINCIPAL_INVESTIGATOR
Rutgers University
Locations
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University Orthopaedic Associates
Somerset, New Jersey, United States
Robert Wood Johnson Somerset Hospital
Somerville, New Jersey, United States
Countries
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Central Contacts
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Facility Contacts
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Stephen Kayiaros, MD
Role: primary
Daniel C Mascarenhas, MD
Role: primary
Other Identifiers
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Pro20140001090
Identifier Type: -
Identifier Source: org_study_id
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