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Status unknownNCT01490606OAUpdated Mar 5, 2012

Knee Osteoarthritis (OA) Project Treatment Versus Conventional Physical Therapy in the Treatment of Knee OA Patients

An interventional study of knee OA project and conventional PT in Osteoarthritis, Knee, sponsored by Meir Medical Center. Status unknown at 1 site in Israel. Open to participants aged 60 Years and older. Per ClinicalTrials.gov, last updated 2012-03-05.

Sponsored by Meir Medical Center · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Mar 2012), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Non-randomized
Ages
60 Years and older
Sex
All
01

Study summary

A. Background.

Patients with osteoarthritis (OA) of the knee, suffer from a combination of pain, stiffness, joint instability, swelling and muscles weakness. This leads to decrease in quality of life, Active Daily living (ADL) and increase of medical services consumption in the community. OA of the knee, Is one of the world's common musculoskeletal disorder (18% among women and 10% among men). 80% of patients with OA of the knee suffer from decrease in mobility and 20% of them suffer an inability to perform everyday activities.

Physical therapy training includes exercises for OA patients (Mild to Severe degree) is the cornerstone of non medicinal treatment. This training aimed to pain reduction, improved functioning and participation in family and working social life. Physical training with exercises can enhance physical capabilities such as: muscular strength, range of motion, balance, proprioception and cardiovascular performance. Other benefits are improving mobility, reducing risk of falls and body weight and improvement in psychological condition.

B. Purpose

The purpose of this research is to check the effectiveness of treatment in the framework of "knee Osteoarthritis project" compared to conventional Physical therapy in physical functioning, pain and quality of life scales, among patients over the age of 60 who suffer from OA of the knee .

C. Research method

A comparative non blinded, clinical trial will be conducted. This research will include 60 independent patients divided into equal groups: Intervention group will be trained in "knee Osteoarthritis project" (in which patients receive 6 individual treatments and 6 Group treatments). Control group will be treated with conventional physical therapy, which includes 12 individual treatments. Effect of the treatment will be evaluated by: 1. WOMAC questionnaire- used to evaluate function and pain. 2. EQ-5D questionnaire for evaluating the quality of life. 3. Time up and go test- a Common functional test. This Questionnaires and test will be Performed before and after the study.

D. Study hypothesis

Physical therapy treatment within the framework of "knee Osteoarthritis project" is favor than the treatment of the conventional Physical therapy. Therefore the investigators expect much improvement in terms of pain, physical functioning and quality of life among intervention group compared to control groups.

Read the detailed description

This research is divided into o Intervention and control groups. Research Population is 60 Patients (30 patients to each arm), aged 60 and above suffering from OA of the knees and admitted to physical therapy .Intervention group patients were treated by the concept of "Knee Osteoarthritis Project". This was first applied in middle of 2010 and its effectiveness was never tested.

The main idea was to make patients more active, to encourage them to do exercise at home, increase their motivation and self efficacy. In addition, patients received prescription for TENS device (Transcutaneous electrical nerve stimulator) for home use.

Individual sessions include: muscle strengthening, proprioception exercise, taping, soft tissue stretching, joint and soft tissue mobilization, electrotherapy, aerobic exercise (bicycle, treadmill), functional exercise. Group session include: muscle strengthening, stairs exercise, balance exercise and education about the disease and treatment (lecture about knee OA and recommendations for changes in life style).

In Intervention group were given 12 session. 6 individual treatments and 6 group treatments Control group patients were given 12 individual sessions of conventional physical therapy.

The Outcome measures that were mention above will be performed in the beginning and the end of 12 sessions.

02

Conditions studied

  • Osteoarthritis, Knee
03

In context

Osteoarthritis

4,398 studies on the registry are indexed under Osteoarthritis; 582 are open to participants now.

This study's planned enrollment of 60 is below the median of 70 across 3,440 interventional studies indexed under Osteoarthritis.

Browse Osteoarthritis studies →

Lead sponsor

Meir Medical Center is the lead sponsor of 389 studies on the registry; 34 are open to participants now.

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

04

Who can participate

Ages eligible
60 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • 60+ years old independent men and women,who suffer from OA in the knee and was referred to Physiotherapy.
  • ability to write and read properly in Hebrew

Exclusion criteria

Exclusion Criteria:

  • OA secondary to systematic disease (Rheumatoid arthritis)
  • steroids injections to the knee in the past 3 months.
  • orthopaedic surgery to lower limbs.
  • neurological deficit.
  • symptomatic OA in the hip or ankle
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    knee OA project

    12 sessions of PT, 6 INDIVIDUAL AND 6 GROUP TREATMENTS

    Other: knee OA project · Other: conventional PT

  • No intervention
    conventional PT

Interventions

  • Otherknee OA project

    physical therapy in "OA Knee project", total of 12 sessions, 6 group therapies amd 6 one on one therapy.

  • Otherconventional PT

    12 SESSIONS OF CONVENTIONAL PHYSICAL THERAPY

06

What researchers measure

Primary outcomes

  1. Time up and go test

    Patient sits on a chair with handles. by order "go", patient will stand up and walk 3 meters forward circle a Conus and return to the chair. a time watch will count time.

    Time frame: On the first week- first session of PT and on last session- 12 weeks Average

  2. WOMAC questionaire

    Time frame: On the first week- first session of PT and on last session- 12 weeks Average

  3. EQ-5D questionaire

    Time frame: On the first week- first session of PT and on last session- 12 weeks Average

Secondary outcomes

  1. Body Mass index

    Time frame: Up to the first week- on the first session of PT

07

Study locations

1 of 1 sites recruiting
  • Clalit Health Service
    Jerusalem, 97802, Israel
    • Shimi Fatal, BPT · Contact · shimifatal@gmail.com · 0504021514
    • Yair Barzilay, MD · Contact · dbar@hadassah.org.il · 0508573279
    • Shimi Fatal, BPT · Sub investigator
    • Yair Barzilai, MD · Principal investigator
    • Ehud Lebel, MD · Sub investigator
    • Esti voltz, BPT · Sub investigator
    • Basma Hasan, BPT · Sub investigator
    • Yaron Milul, M.A · Sub investigator
    • Goni Miron, M.A · Sub investigator
    • Tal Shemesh, M.A · Sub investigator
    • Lisa Cohen, M.A · Sub investigator
    • Alexandra Maximov, BPT · Sub investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 5, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01490606
Lead sponsor
Meir Medical Center
Responsible party
Shemtov Fatal (physical therapist, Meir Medical Center) — Principal investigator
First posted
Dec 13, 2011
Start date
Jan 2012
Primary completion
Sep 2012 (estimated)
Completion
Dec 2012 (estimated)
Last update
Mar 5, 2012

Study contacts

Shimi Fatal, BPT
Contact
shimifatal@gmail.com
0504021514
Yair barzilai, M.D
Contact
dbar@hadassah.org.il
0508573279
Yair Barzilai, M.D.
principal investigator · Clalit health service, Israel

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Mar 2012. You cannot join it, but the record below documents what was studied.

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