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Unrestricted Rehabilitation Following Primary THA

NCT02079467 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2014-03-05

No results posted yet for this study

Summary

The purpose of this study is to determine whether the form of rehabilitation following primary total hip arthroplasty has an influence on patient satisfaction or functional performance in the eighteen weeks following surgery.

Conditions

  • Osteoarthritis, Hip

Interventions

PROCEDURE

Unrestricted rehabilitation

Standard care range of motion restrictions will not be used

PROCEDURE

Standard rehabilitation

Standard care range of motion restrictions will remain in place

Sponsors & Collaborators

  • Sunnybrook Health Sciences Centre

    lead OTHER

Principal Investigators

  • Hans J Kreder, MD MPH FRCSC · Sunnybrook Health Sciences Centre, University of Toronto

  • Richard Jenkinson, MD MSC FRCSC · Sunnybrook Health Sciences Centre, University of Toronto

  • Veronica MR Wadey, BPHE BEd MD MA FRCSC · Sunnybrook Health Sciences Centre, University of Toronto

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-12-31
Primary Completion
2014-06-30
Completion
2014-11-30

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02079467 on ClinicalTrials.gov