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Prehabilitation to improve outcomes for patients undergoing hip and knee replacement surgery.

The effect of prehabilitation compared to usual care on functional outcomes and health service resource use in clients eight weeks following total knee or hip arthroplasty surgery

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12610000777099
Enrollment
60
Registered
2010-09-17
Start date
2010-09-21
Completion date
2011-11-30
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Currently, patients undergoing hip and knee replacement surgery do not participate in formal exercise classes prior to their operation. It is possible that the introduction of these classes may affect patients’ length of inpatient hospital stay, discharge destination, the speed of post-operative improvement (particularly movement of the affected joint) and the use of healthcare resources. Participation in exercise classes may also improve health-related quality of life following surgery. This pilot project will examine the effect of an exercise group for patients undergoing elective hip and knee replacement surgery provided prior to their surgery (referred to herein as ‘prehabilitation’). Patients attending pre-admission clinic prior to their operation will be invited to participate in the study and included participants will be randomized to either usual care or usual care with the addition of prehabilitation. All participants will undergo baseline testing of health-related quality of life, joint range of movement and functional activity testing in pre-admission clinic and participants will then be re-tested eight weeks following their operation. The differences between groups (usual care and usual care + prehabilitation) will be analysed using appropriate statistical tests.

Interventions

Prehabilitation sessions will be 60 minutes in duration conducted by a physiotherapist. The program will be conducted twice weekly, for up to 4 weeks prior to the patients surgery date, with a maximum 6 clients per group. The exercise component will take a circuit training approach where various stations are set out that participants move around during the session. These exercises will include 1. Warm up for all at rails in standing (5 minutes) 2. Plinth – Hip knee flexion/quads over fulcrum/H

Prehabilitation sessions will be 60 minutes in duration conducted by a physiotherapist. The program will be conducted twice weekly, for up to 4 weeks prior to the patients surgery date, with a maximum 6 clients per group. The exercise component will take a circuit training approach where various stations are set out that participants move around during the session. These exercises will include 1. Warm up for all at rails in standing (5 minutes) 2. Plinth – Hip knee flexion/quads over fulcrum/Hip Abduction/Bridging 3. Chair – Knee flexion and extension 4. Rails – gait re-education 5. Rails – Hip abduction/ Hip Flexion/ Hip Extension/ Squats/ Heel Raises/ Ham string curls/ calf stretch 6. Pedals/stairs/exercise bike 7. Lunges 8. Hands on therapy on plinth with Physiotherapist (Usual care rehabilitation phase) / Education station (prehabilitation phase) Despite the circuit format, all of these exercises will have individually tailored dosages / difficulty levels set to ensure that therapeutic benefit and participant safety are maximized. Education will also be provided to participants through provision of hip and knee care booklets with a view to clarifying the operation, pain management, gait aids, (giving a general post-surgical concept) as well as educating the patient regarding ongoing exercise at home. Participants allocated to the intervention group will also be given a “passport” which they will be required to bring to all appointments eg. Community rehabilitation centre, their hospital inpatient stay, to have their attendance recorded and signed off by staff.

Sponsors

Southern Health
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
0 to No maximum
Healthy volunteers
No

Inclusion criteria

Any patient undergoing a total hip replacement or total knee replacement at Monash Medical Centre Moorabbin or Dandenong Hospital who lives within the Greater Dandenong & Springvale catchment area. Risk Assessment and Prediction Tool (RAPT) score >6.

Exclusion criteria

Any patient undergoing a total hip replacement or total knee replacement at Monash Medical Centre Moorabbin or Dandenong Hospital who does not live within the Greater Dandenong & Springvale catchment area. If patient surgery less than three weeks away. Unable to follow instructions/ not suitable for group setting Revision surgeries. Corticosteroid injection in previous six months. Wheelchair bound patients

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026