Hydrotherapy Versus Physiotherapy for Short-term Rehabilitation After Primary TKR

This study has been completed.
Sponsor:
Information provided by:
Hadassah Medical Organization
ClinicalTrials.gov Identifier:
NCT00878358
First received: April 7, 2009
Last updated: April 27, 2011
Last verified: April 2009
  Purpose

Primary objective:

To compare the effects of short term therapy post total knee replacement (TKR) between a hydrotherapy treatment group and a physiotherapy treatment group.

Secondary objectives:

To compare the effects of short term therapy post total knee replacement (TKR) between a hydrotherapy treatment group and a physiotherapy treatment group based on measurements of timed up and go (TUG, as primary outcome), range of motion, pain and quality of life.


Condition Intervention
Osteoarthritis
Total Knee Replacement
Other: Hydrotherapy
Other: Physiotherapy

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Hydrotherapy Versus Physiotherapy for Short-term Rehabilitation After Primary TKR

Resource links provided by NLM:


Further study details as provided by Hadassah Medical Organization:

Primary Outcome Measures:
  • Timed up and go test [ Time Frame: 6 weeks ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Oxford knee score [ Time Frame: 6 weeks ] [ Designated as safety issue: No ]
  • Visual analogue pain score [ Time Frame: 6 weeks ] [ Designated as safety issue: No ]
  • Range of knee motion [ Time Frame: 6 weeks ] [ Designated as safety issue: No ]

Estimated Enrollment: 100
Study Start Date: June 2009
Study Completion Date: June 2010
Primary Completion Date: April 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Physiotherapy Other: Physiotherapy
Experimental: Hydrotherapy Other: Hydrotherapy

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Candidates for first total knee replacement surgery.

    • Age over 18.
    • Diagnosed with Osteoarthritis.
    • Consent to participate in the trial.

Exclusion Criteria:

  • - Rheumatic diseases.
  • Neurological diseases involving lower limbs.
  • Prior knee surgery in operated knee.
  • Secreting surgical wound.
  • Skin diseases.
  • Incontinence.
  • Incapable of signing informed consent.
  • Patients living outside Jerusalem
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00878358

Locations
Israel
Hadassah Medical Organization
Jerusalem, Israel
Sponsors and Collaborators
Hadassah Medical Organization
  More Information

No publications provided

Responsible Party: Leonid Kandel, Hadassah Medical Center
ClinicalTrials.gov Identifier: NCT00878358     History of Changes
Other Study ID Numbers: Hydrotherapy-HMO-CTIL
Study First Received: April 7, 2009
Last Updated: April 27, 2011
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration

Keywords provided by Hadassah Medical Organization:
Osteoarthritis
Total knee replacement

Additional relevant MeSH terms:
Osteoarthritis
Arthritis
Joint Diseases
Musculoskeletal Diseases
Rheumatic Diseases

ClinicalTrials.gov processed this record on September 18, 2014