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Knee rehabilitation: home visual feedback and video call follow up

Community­ based visual feedback of motion during rehabilitation exercises and video call follow up with hospital based therapists following total knee joint replacement (TKR) surgery: a pilot randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN33424520
Enrollment
60
Registered
2012-11-27
Start date
2012-11-19
Completion date
Unknown
Last updated
2017-07-03

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

Conditions

Knee Replacement Rehabilitation Surgery

Interventions

Control Group This group will receive the usual care i.e. exercise booklet / DVD for the home exercises and a phone call from the hospital outcomes team 10-14 days after discharge. Intervention Group

Sponsors

Golden Jubilee National Hospital (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Adult patients who would have consented to undergo a first unilateral primary total knee replacement at Golden Jubilee National hospital.

Exclusion criteria

Exclusion criteria: 1. Patients listed for second or bilateral knee replacement or revision surgery 2. Patients unable to give informed written consent 3. Patients who are geographically located outside of 2 hours radius from Glasgow city centre. Transportation to patients? homes for setups and training should not take too long for the researcher. 4. Patients who have severe visual, perceptual or cognitive problems as participants should be able to use and see the visualisation and video conferencing equipment after being trained. 5. Patients who are involved in any other intervention as these may influence the outcomes and be a source of additional stress for participants. 6. Patients who are referred for outpatient physiotherapy. This gives rise to the possibility of a patient being excluded after consent has already being provided. As a consequence the patient information sheet will contain a clause informing the patient of the likelihood of being excluded as a result of postoperative outcomes.

Design outcomes

Primary

MeasureTime frame
Difference in walking speed at baseline (1st week) and at 6th week.

Secondary

MeasureTime frame
1. Timed up and go test 2. Oxford knee score 3. Quality of life i.e. SF-12 and EQ-5D 4. Active range of motion of the knee joint 5. Absence of knee extension lag 6. Adherence to rehabilitation exercises

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026