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Not yet recruitingNCT07502040KEMTAIUpdated Mar 30, 2026

Impact of Exercise Access on Physio Outcomes Post Knee Replacement

An interventional study of Kemtai Digital App and NHS standard care in Knee Arthroplasty, Total, sponsored by Hull University Teaching Hospitals NHS Trust. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-03-30.

Sponsored by Hull University Teaching Hospitals NHS Trust · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

To stay strong, patients should do some strength training at least twice a week. However arthritic pain can limit walking and activity. The wait for knee surgery can be long, which can lead to loss of muscle strength. Patients who need a new knee joint tend to be older. If older people do not exercise and become weak, they tire easily, and may take longer to recover after surgery. Patients recover faster after having a new knee joint if their leg muscles are strong. This is why exercise before surgery can help people to make the most of their new joint. Patients come to a joint school where the investigators show them exercises and advise how to get ready for surgery. Patients are given a sheet of pictures and prompts for each exercise but the investigators know that some people don't do the exercises that they are given. Exercises are more likely to be done if they are fun, if people can see they make a difference, if they know what to do, and if their physiotherapist can check what they are doing.

Read the detailed description

To stay strong, patients should do some strength training at least twice a week. However arthritic pain can limit walking and activity. The wait for knee surgery can be long, which can lead to loss of muscle strength. Patients who need a new knee joint tend to be older. If older people do not exercise and become weak, they tire easily, and may take longer to recover after surgery. Patients recover faster after having a new knee joint if their leg muscles are strong. This is why exercise before surgery can help people to make the most of their new joint. Patients come to a joint school where the investigators show them exercises and advise how to get ready for surgery.

Patients are given a sheet of pictures and prompts for each exercise but the investigators know that some people don't do the exercises that they are given. Exercises are more likely to be done if they are fun, if people can see they make a difference, if they know what to do, and if their physiotherapist can check what they are doing.

Patients come to a joint school where the investigators show them exercises and advise how to get ready for surgery. Patients are given a sheet of pictures and prompts for each exercise but the investigators know that some people don't do the exercises that they are given. Exercises are more likely to be done if they are fun, if people can see they make a difference, if they know what to do, and if their physiotherapist can check what they are doing.

Kemtai is an online exercise program which shows how to do the exercises and tells the patient how to move in the right way if they are not doing it correctly. The patient gets a score to show how well they are doing the exercise. This makes the task fun. Their physio can see when they have exercised and if they are making progress.

The investigators will perform a small study called a pilot randomised controlled trial to find out how many people are eligible to take part, how many agree to take part, and the reasons for not being able to do so.

This study will tell us how many patients can use online programmes and have access to computers, tablets or smartphones that can run the Kemtai programme. The investigators can provide data if someone is able to take part but are unable to provide a smartphone or tablet. This study will tell us how many patients would need data or devices to take part in a bigger study.

The investigators also want to know if there are any differences in amount of exercise done before surgery, and in length of stay in hospital, amount of physiotherapy, pain, movement and quality of life after surgery between those who used a paper exercise prompt sheet and those who used an online exercise programme (Kemtai).

Joint school physios will identify who is eligible for the study. If interested, the patients will be given a leaflet and invited to watch a presentation about the study. Those patients who wish to take part will be asked to give informed consent and asked to fill in three questionnaires (Oxford knee score, EQ-5D-5L and the visual analogue scale). Patients will also be asked for some information (name, address, gender, ethnic group, e-mail, and year of birth) to help the investigators compare the two groups. A computer programme will inform the investigators if the patient should have Kemtai access or a sheet of exercises. No more physiotherapy is given until after the patients have their new joint. The investigators offer help to access the Kemtai programme and will note what help is needed.

After surgery, the number of physio contacts and the number of hours in hospital will be counted. The number of times that the patients exercised before surgery will be collected either from the exercise diary that contains the paper exercise list, or from the Kemtai programme. At six weeks after surgery patients will be contacted by phone and asked to give their scores for the three questionnaires again. A patient's time in the study stops at this point.

A team, which includes patients who have had new knee joints, will look at the results and decide how a larger study should be run.

02

Conditions studied

  • Knee Arthroplasty, Total

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Keywords

  • Arthroplasty
  • Exercise
  • Prehabilitation
  • Motion-tracking
  • Digital App
  • Artificial intelligence
03

In context

Motor Activity

2,426 studies on the registry are indexed under Motor Activity; 1,161 are open to participants now.

This study's planned enrollment of 40 is below the median of 60 across 2,118 interventional studies indexed under Motor Activity.

Browse Motor Activity studies →

Lead sponsor

Hull University Teaching Hospitals NHS Trust is the lead sponsor of 93 studies on the registry; 15 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Adults aged ≥18 years.
  2. Referred to Hull University Teaching Hospitals NHS Trust t for Knee Arthroplasty at either Castle Hill Hospital or Goole District Hospital and has access to pre operative resources offered by the joint school physiotherapists.
  3. Has access to a device which is compatible with the operational requirements of the Kemtai programme.
  4. Able to give informed consent.

Exclusion criteria

Exclusion Criteria:

  • Significant comorbid physical or mental illness considered by the investigator to either: prevent engagement in modified exercise; impair the participants ability to follow instructions place the participant at undue risk during exercise training adversely affect the recovery or rehabilitation trajectory
  • Patients already involved in an exercise or rehabilitation study will be excluded from this study.
  • Unwilling or unable to consent or complete study measures.
  • Has insufficient understanding of English or the languages that are supported by the Kemtai programme and does not have someone who can translate.
  • Is a prisoner
  • Has had a total hip replacement within the previous 6 months.
  • Is attending for revision of a previous knee replacement
  • Is having a knee replacement due to a tumour
  • Lacks visual acuity sufficient to follow stimuli on monitor or has someone who can give necessary verbal prompts
  • Severe genu varum or genu valgum deformity which precludes the ability to exercise using the Kemtai programme.
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    Kemtai Digital App

    A randomised group of twenty patients will be granted access to the Kemtai digital App (the experimental arm) which provides an identical exercise prescription to the comparator (NHS standard of care intervention) but supports the patient through the exercise with tracking and real time (via AI) advice on corrective exercise techniques.

    Device: Kemtai Digital App

  • Active comparator
    NHS Standard of Care

    A randomised group of twenty patients will be provided the NHS standard of care which is a paper based handout illustrating the exercises and the prescription to be done before and after surgery.

    Behavioral: NHS standard care

Interventions

  • DeviceKemtai Digital App

    This group will be granted access to the Kemtai digital App (the experimental device intervention) which provides an identical exercise prescription to the comparator intervention but supports the patient through the exercise with tracking and real time (mediated via AI) advice on corrective exercise techniques.

  • BehavioralNHS standard care

    This group will be provided the NHS standard of care which is a paper based handout illustrating the exercises and the prescription to be done before and after surgery.

06

What researchers measure

Primary outcomes

  1. Length of stay in hospital

    Number of hours between time of surgery and time of discharge

    Time frame: From time of surgery to the time of discharge from hospital, up to 52 weeks.

  2. Number of post operative physiotherapy contacts

    This measure is a count of the number of times that the participant has a documented contact with a physiotherapist after surgery. This may be in person or via telephone or video call, and may take place in hospital or after discharge from hospital after surgery.

    Time frame: From operation to 6 weeks post operation, up to 52 weeks.

Secondary outcomes

  1. Oxford knee scale

    The Oxford Knee Score (OKS) is a validated 12-question patient survey used to assess pain and functional limitations in patients with knee arthritis. Scores range from 0-48, with lower score indicating more pain and functional limitations.

    Time frame: From enrolment to six weeks post surgery

  2. EQ5DL- a health-related quality of life tool.

    The EQ5DL is a well validated quality of life measure. The scoring is 1-5 across each domain (mobility, self-care, usual activities, pain/discomfort and anxiety/depression) with a higher number indicating worse quality of life in each domain. Scoring: Results in a 5-digit code (e.g., 11111 for excellent quality of life and 5,5,5,5,5 for the worst quality of life

    Time frame: From enrolment to six weeks post surgery, up to 52 weeks.

  3. Visual analogue scale

    Includes a visual analogue scale (0-100) for patients to rate their health "today". A higher score is indicates better health.

    Time frame: From enrolment to six weeks post surgery

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Yes — We will share anonymised data with other researchers. Any request for data should be made to Dr Angela Green at Angela.Green28@nhs.net or Dr James P Hobkirk at James.Hobkirk3@nhs.net

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 30, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07502040
Lead sponsor
Hull University Teaching Hospitals NHS Trust
Responsible party
Sponsor
First posted
Mar 30, 2026
Start date
Mar 31, 2026 (estimated)
Primary completion
Sep 30, 2026 (estimated)
Completion
Nov 28, 2026 (estimated)
Last update
Mar 30, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2025. You cannot join it, but the record below documents what was studied.

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