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Status unknownNCT00668915Updated Apr 29, 2008

Arthroplasty Rehabilitation Score - Can we Predict the Short Term Postoperative Outcome?

An observational study in Osteoarthritis, sponsored by Hadassah Medical Organization. Status unknown at 1 site in Israel. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2008-04-29.

Sponsored by Hadassah Medical Organization · Observational

The sponsor has not verified this record recently (last verified Apr 2008), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
200
Ages
18 Years and older
Sex
All
01

Study summary

Total joint arthroplasty are common operations among the elderly population. The postoperative patients' rehabilitation process may be influenced by a variety of factors, such as age, BMI, perioperative hemoglobin levels, pain perception, comorbidities, etc. Nevertheless, only a few well controlled studies evaluated the effect of various factors on patients' rehabilitation short-term outcome. Furthermore, no scale has been developed, that can predict patients' rehabilitation and functioning levels 6 weeks postoperatively. In the current study we wish to evaluate the effect on patients' function that the following factors have: age, BMI, admission and discharge hemoglobin levels, pain perception, type of operation (TKA versus THA), intensity of postoperative physiotherapy, involvement of other joints by the primary pathology, comorbidities, and self assessed health status.

In order to quantify patients' level of functioning, several tests will be used: hand grip strength, Timed up and go test (TUG) and Oxford knee and hip score. The factors that will be found statistically significantly associated with level of functioning, will be used in an attempt to develop a scale that will predict the level of functioning 6 weeks postoperatively.

Such a scale can allow preoperative identification of patients at high risk of postoperative low functioning levels and the application of a unique rehabilitation program, for only these patients, in order to optimize their functioning.

Read the detailed description

This is a prospective, analytical, approximately 6 months long study.

Population:

Approximately a 100 patients, scheduled for an elective arthroplasty will be recruited for the study:

  • Males and females above 18 years of age, speaking Hebrew, English or Russian, scheduled for an elective unilateral (one joint) primary total joint arthroplasty of hip or knee.
  • Available for follow up 1.5-2 months after the surgery.
  • Willing to participate in the study.

Inclusion criteria:

  1. Patient above the age of 18 and eligible to provide informed consent.
  2. Scheduled for elective unilateral (one joint), primary total joint arthroplasty of hip or knee.
  3. Stepping with the operated leg is allowed after the surgery.

Exclusion criteria:

  1. Patients unwilling to participate.
  2. Patients with complications preventing regular rehabilitation, e.g. Myocardial Infarction, Pulmonary Embolism, Pneumonia, and infection or fracture of the joint.
  3. Patients with any complication that prevents stepping with the operated leg.

Design:

  1. Prior to the scheduled operation, the following data regarding the patient will be collected:

    • Gender, age, height, weight.
    • Comorbidities (using Katz Score).
    • Type of scheduled operation.
    • Involvement by the primary pathology of joints other than the one being operated (by patient questioning).
    • Hemoglobin level at admission.
    • Self assessed health status (by patient questioning).
    • Pain perception in the operated leg (using VAS Score).

    In addition, the following tests will be performed:

    • Evaluation of muscle strength using handgrip machine.
    • Evaluation of motor functioning level using the TUG test and the Oxford knee and hip score.
  2. During the postoperative hospitalization period, hemoglobin and CRP levels will be checked, and the patients will be evaluated for complications.
  3. In the follow up visit, the following data will be collected:

    • Complications after discharge from hospital.
    • Blood transfusions in this period.
    • Duration of time in rehabilitation program, and intensity of physiotherapy given.

During the visit, the following tests will be performed:

  • Evaluation of muscle strength using handgrip machine.
  • Evaluation of motor functioning level, similar to the one performed preoperatively, using the TUG test and the Oxford knee and hip score.
02

Conditions studied

  • Osteoarthritis

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03

In context

Osteoarthritis

4,445 studies on the registry are indexed under Osteoarthritis; 582 are open to participants now.

This study's planned enrollment of 200 is above the median of 100 across 803 observational studies indexed under Osteoarthritis.

Browse Osteoarthritis studies →

Lead sponsor

Hadassah Medical Organization is the lead sponsor of 674 studies on the registry; 55 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients undergoing primary arthroplasty

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Patient above the age of 18 and eligible to provide informed consent.
  2. Scheduled for elective unilateral (one joint), primary total joint arthroplasty of hip or knee.
  3. Stepping with the operated leg is allowed after the surgery.

Exclusion criteria

Exclusion Criteria:

  1. Patients unwilling to participate.
  2. Patients with complications preventing regular rehabilitation, e.g. Myocardial Infarction, Pulmonary Embolism, Pneumonia, and infection or fracture of the joint.
  3. Patients with any complication that prevents stepping with the operated leg.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
200 participants (estimated)

Groups and cohorts

  • A

    Primary arthroplasty

06

What researchers measure

Primary outcomes

  1. Oxford hip and knee score

  2. Grip strength

  3. Timed up and go test

07

Study locations

1 site
  • Hadassah Medical Organization
    Jerusalem, Israel
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 29, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00668915
First posted
Apr 29, 2008
Last update
Apr 29, 2008

Study contacts

Leonid Kandel, MD
Contact
kandel@hadassah.org.il
972-50-787-4328

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Apr 2008. You cannot join it, but the record below documents what was studied.

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