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Preoperative Pain, Function, and Activity for Total Hip and Knee Arthroplasty Patients

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ClinicalTrials.gov Identifier: NCT01248039
Recruitment Status : Completed
First Posted : November 25, 2010
Last Update Posted : July 19, 2012
Sponsor:
Collaborator:
Lundbeck Foundation
Information provided by (Responsible Party):
Bente Holm, Hvidovre University Hospital

Brief Summary:
This study wish to show if the preoperative level of pain, function or activity for hip and knee arthroplasty patients has any predictive value of the time it takes to fulfill the well-defined discharge criteria.

Condition or disease
Arthroplasty

Detailed Description:
The investigators would like to be able to identify those patients, for whom it will take longest time to fulfill the discharge criteria. With this knowledge the investigators will be able to initiate sufficient treatment already before operation.

Study Type : Observational
Estimated Enrollment : 100 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: The Influence of Preoperative Pain, Function, and Activity on Time to Fulfill Discharge Criteria for Total Hip and Knee Arthroplasty Patients
Study Start Date : January 2011
Primary Completion Date : July 2012
Study Completion Date : July 2012

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Knee Replacement
U.S. FDA Resources

Group/Cohort
Total arthroplasty
Patients with osteoarthrosis going for hip or knee arthroplasty



Primary Outcome Measures :
  1. Leg muscles strength [ Time Frame: 7 months ]
    Maximal muscle force tested for one leg at a time in a Power Rig Mashine


Secondary Outcome Measures :
  1. Functional performance [ Time Frame: 7 months ]
    Tested by: Timed Up & Go test, 10 meter fast speed walking test



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Concesutive hip and knee arthroplasty patients from a department of orthopaedic surgery
Criteria

Inclusion Criteria:

  • Total hip arthroplasty patients
  • Total knee arthroplasty patients

Exclusion Criteria:

  • Inability to speak and understand Danish
  • Inability to perform the functional measurements due to other conditions

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01248039


Locations
Denmark
Department of Surgery, Univerity Hospital at Hvidovre
Hvidovre, Denmark, 2650
Sponsors and Collaborators
Hvidovre University Hospital
Lundbeck Foundation
Investigators
Principal Investigator: Bente Holm, MSc The Lundbeckcenter for hip and knee surgery, University Hospital at Hvidovre, Kettegaard Allé 30, DK-2650 hvidovre, Denmark

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Bente Holm, Physiotherapist for development and research, Hvidovre University Hospital
ClinicalTrials.gov Identifier: NCT01248039     History of Changes
Other Study ID Numbers: H-4-2010-FSP2
PRE-THA-TKA ( Registry Identifier: H-4-2010-FSP2 )
First Posted: November 25, 2010    Key Record Dates
Last Update Posted: July 19, 2012
Last Verified: July 2012

Keywords provided by Bente Holm, Hvidovre University Hospital:
Muscle strength, functional performance, joint replacement