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Clinical Trials/ACTRN12616000054415
ACTRN12616000054415
Completed
未知

Effect of telephone-delivered advice on pain and function in people with knee osteoarthritis: Telecare trial

The University of Melbourne0 sites175 target enrollmentJanuary 20, 2016

Overview

Phase
未知
Intervention
Not specified
Conditions
Knee Osteoarthritis
Sponsor
The University of Melbourne
Enrollment
175
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 20, 2016
End Date
October 25, 2018
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Participants aged 45 years or over with painful knee osteoarthritis (OA) will be recruited. People will be eligible if they report average knee pain of at least 4 on 11\-point numerical rating scale (NRS), have had knee pain for greater than 3 months, have activity\-related joint pain and have morning stiffness \<30 minutes duration.

Exclusion Criteria

  • \- on the waiting list for a knee or hip replacement, or planning any lower limb or spinal surgery in the coming 12 months
  • \- have had a knee joint replacement in the affected knee
  • \- undergone knee surgery in the prior 3 months
  • \- currently undertaking exercise prescribed by a health professional in the past 6 months
  • \- unable to speak or read English
  • \- unable to use/access a telephone
  • \- self\-reported diagnosis of rheumatoid arthritis
  • \- any neurological condition (such as stroke, multiple sclerosis, polio, a neuropathy, peripheral nerve disease, Parkinson’s disease) that affects ability to exercise safely
  • \- any cardiovascular condition (such as unstable cardiac disease, uncontrolled hypertension, uncontrolled metabolic disease, abdominal aortic aneurysm)
  • \- fail pre\-exercise screening (consists of seven questions which are answered YES or NO, and are designed to identify individuals with signs or symptoms of underlying disease, or who may be at higher risk of an adverse event during exercise)

Outcomes

Primary Outcomes

Not specified

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