None listed
Conditions
Brief summary
Participants will be randomly allocated in a 1:1:1 ratio to receive either i) control (usual care); ii) a prescribed home program with one strength exercise or; iii) a prescribed home program with multiple (five) exercises. The control group will not receive any intervention and will continue with their usual care. Participants in the exercise groups will have three video-conferencing consultations with a physiotherapist (week 1-, 2- and 6-weeks post-randomisation, 30 minutes each) for prescription, monitoring and progression of their exercise program, which will be performed independently at home for 3 months. Participants in the exercise groups will be encouraged to continue with exercises beyond the intervention period. Primary time-point for re-assessment will be 3 months, with a secondary time-point of 9 months, after randomisation. The primary outcome measure will be change in average walking pain over the past week on NRS. Secondary outcome measures will include WOMAC pain and function subscales, quality-of-life; arthritis and exercise self-efficacy; fear of movement; global rating of change; muscle strength; willingness for joint replacement.
Interventions
Active exercise groups Participants will be randomly assigned a physiotherapist (stratified by group allocation - ‘one’ or ‘five’ exercise arm using random permuted block sizes) and research staff will book three consultation appointments (1, 2 and 6 weeks post-randomisation, 30 minutes each) on behalf of the participant. The consultations with the physiotherapist will occur via telehealth (Zoom video- conferencing), for prescription, monitoring and progression of a home strength program that participants will be asked to undertake for 12 weeks, but encouraged to continue beyond that time up until 9 months. Physiotherapists will be permitted to use their clinical judgement to prescribe exercise(s) from a pre-determined list of allowed exercises that reflects the typical home strength exercises prescribed in the literature for knee OA and by physiotherapists in Australia. Physiotherapists will be asked to prescribe the exercise(s) that they think will be most beneficial in relieving pain and improving function for a given participant. Exercises will be selected from a list including quadriceps exercises (including weightbearing such as squats and non-weightbearing exercises such as seated knee extensions), hamstrings exercises (such as hamstring curls or seated knee flexion), hip exercises (such as crab walking or bridges) and calf exercises (such as calf raises). Participants will be asked to perform prescribed exercises at home (3 sets of 12 repetitions for each exercise), three times/week. The only difference across trial arms is in the number of exercises that will be prescribed (one versus five as per the randomisation schedule). The physiotherapist will individualise the technique of each exercise (e.g. depth of knee bend, amount of body weight, hold time, colour of exercise band etc) to encourage the participant to work at an intensity of 5-7 out of ten (hard to very hard) on the modified Borg Rating of Perceived Exertion CR-10 scale for strength training. At subsequent consultations, physiotherapists may replace a prescribed exercise(s) for a different exercise(s) if required (eg because an exercise is too easy, too hard, aggravates the knee etc) as long as they adhere to the allocated number of exercises (ie a participant’s program contains only the allocated number of exercises of either one or five) and choose only from the defined list of exercises. Consultations will occur via the video-conferencing facility of Zoom, a commercial cloud-based system accessible from any internet-connected computer, laptop or mobile device. Physiotherapists will consult from their clinic with participants based at home or wherever is suitable (e.g. work). Physiotherapists will be provided access to a website containing a video library of exercises to allow them to provide real-time demonstration of exercises to participants. This will be shared with the participants via a share-screen feature on Zoom so that the participant is able to view a demonstration of the exercise during the consultations. Participants will not have access to the online video library outside of the consultations. During each consultation, physiotherapists will email participant’s exercise handouts for how to perform each of their prescribed exercises (the research team will provide the physiotherapists with standardised digital instructions for each exercise on the allowed list of exercises to facilitate this). Semi-structured electronic consultation notes will be recorded by the physiotherapist for each consultation and submitted to research staff at the completion of each consultation. Notes will be scrutinised by research staff for physiotherapist fidelity to exercise protocols.
Sponsors
Study design
Eligibility
Inclusion criteria
i) meet National Institute for Health and Care Excellence clinical criteria for Osteoarthritis (OA) a. age 45 years or over; b. activity-related knee joint pain; c. no morning knee stiffness or morning knee stiffness duration of 30 mins or less; ii) report history of knee pain of 3 months or longer; iii) report knee pain on most days of the past month; iv) report knee pain on walking over past week of 4 or more on 11-point (0-10 range) numerical rating scale (NRS); v) report difficulty walking or climbing stairs; vi) have an email address for receiving exercise instruction sheets; vii) have access to a computer/laptop/tablet/smartphone with webcam and internet connection for Zoom consultations and; viii) willing to participate in video consultations for physiotherapy appointments.
Exclusion criteria
i) inability to speak or read English; ii) on waiting list for/planning knee/hip surgery in next 9 months; iii) previous arthroplasty on affected knee; iv) undergone knee surgery in the past 6 months; v) is undertaking/has undertaken regular strengthening exercise (at least once per week) for knee problems at any stage in the past 6 months; vi) intending to/planning to commence regular strengthening exercise (at least once per week) for knee problems in the next 3 months; vii) self-reports any inflammatory arthritis (e.g., rheumatoid arthritis); viii) self-reports any neurological condition that impacts their lower limb function or; ix) self-reports any unstable/uncontrolled cardiovascular condition that could make exercise unsafe. x) previously participated in a CHESM clinical trial in the prior four years, or currently participating in another research study at CHESM or elsewhere.