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Efficacy of Preoperative Muscle Training on Postoperative Orthopaedic Surgery Recovery

O

Ottawa Hospital Research Institute

Status

Completed

Conditions

Osteoarthritis
Arthroplasty

Treatments

Other: Rehabilitation
Other: Standard of Care

Study type

Interventional

Funder types

Other

Identifiers

NCT03483519
20150684

Details and patient eligibility

About

The purpose of this study is to assess the effectiveness of a preoperative muscle training program on hip or knee TJA (Total Joint Arthroplasty). It aims to improve hospital discharge readiness and functional capacity in both the short and long-term. One of the key factors affecting recovery after TJA is how well the patient functions before their surgery. Thus, interventions addressing preoperative function are expected to be beneficial.

Full description

Although total hip or knee joint replacement is beneficial in treating severe hip or knee osteoarthritis, a significant number of patients take longer to recover in the hospital or have a non-optimal quality of life after the surgery. These patients often have difficulties in accomplishing basic essential everyday tasks such as walking and stair climbing, both shortly and long after surgery. It has been previously shown through research that difficulties to do basic tasks before surgery delays recovery and negatively affects long-term function. It has also been shown that these difficulties are associated with reduced strength in hip or knee muscles present before surgery, caused by lack of activity of patients. This study will determine if a hip or knee muscle strengthening exercise program accomplished before surgery can improve hospital recovery, capacity to accomplish basic activities, and quality of life two days, six weeks and six months after joint replacement surgery. If this exercise program is shown to be beneficial, it will be easily used by patients when waiting for their surgery.

Enrollment

55 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients aged 18 and older undergoing unilateral total hip or knee arthroplasty due to osteoarthritis;
  • WOMAC functional subscale less than 66.5/100.

Exclusion criteria

  • Patients under 18 years of age;
  • Patients undergoing joint revision on the affected side;
  • patients under the same day discharge protocol;
  • Patients undergoing bilateral arthroplasty;
  • Patients suffering from other previously diagnosed lower-limb problems limiting their capacity to accomplish the exercise program;
  • Patients having surgery in less than 16 weeks after verbal consent;
  • Patients unable or unwilling to commit to required study follow-ups;
  • Patients with no fixed address;
  • Patients with a cognitive impairment that may preclude questionnaire completion;
  • Pregnant or suspected pregnant women as dual-energy x-ray (DXA) used in this study may be harmful to a fetus.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

55 participants in 2 patient groups

Prehabilitation
Experimental group
Description:
Patients in the Prehabilitation Group and are randomized to the Experimental Group will undergo a 6 Week Exercise Program plus Standard of Care
Treatment:
Other: Rehabilitation
Standard of Care
Active Comparator group
Description:
Patients in the Standard of Care will not receive an additional an exercise program, patients will receive the usual care received by all orthopaedic patients.
Treatment:
Other: Standard of Care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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