Trial · NCT07912333
Wearable Device Guided Exercise for Patients on Total Knee Arthroplasty Wait-list
NCT07912333, Not applicable, Not yet recruiting, Chinese University of Hong Kong
3 sourcestrials-2026-11-12-0.4.0
Cite this record
ConductScience Library. Wearable Device Guided Exercise for Patients on Total Knee Arthroplasty Wait-list. Trials, record NCT07912333. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07912333
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Wearable Device Guided Exercise for Patients on Total Knee Arthroplasty Wait-list
- NCT number
- NCT07912333
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 106 participants, estimated
- Lead sponsor
- Chinese University of Hong Kong
- Conditions
- Knee Osteoarthristis
- Interventions
- Wearable Device, Control
- First posted
- 2026-11-03
- Last updated
- 2026-11-03
Source ClinicalTrials.gov
Registered outcomes10
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Knee Injury Osteoarthritis Outcome Score (KOOS) | baseline, 6 weeks and 6 months | 10 minute self completed questionnaire measuring five sub-scales: Pain, other Symptoms, Function in daily living (ADL), Function in Sport and Recreation (Sport/Rec), and knee-related Quality of Life (QOL). Each sub-scale scored from 0 to 100, with 100 being no complaints. |
| Secondary | Knee Flexion during walking | baseline, 6 weeks and 6 months | Patients walk and have their knee flexion measured using optical motion capture, outcome in degrees. |
| Secondary | Hip Flexion during walking | baseline, 6 weeks and 6 months | Patients walk and have their hip flexion measured using optical motion capture, outcome in degrees. |
| Secondary | Knee Flexion during sit-to-stand | baseline, 6 weeks and 6 months | Patients does sit-to-stand and have their knee flexion measured using optical motion capture, outcome in degrees. |
| Secondary | Hip Flexion during sit-to-stand | baseline, 6 weeks and 6 months | Patients does sit-to-stand and have their hip flexion measured using optical motion capture, outcome in degrees. |
| Secondary | 30 seconds chair to stand test | baseline, 6 weeks and 6 months | Participant sat on on a chair then execute repetitive sit-to-stand movement as much as possible within 30 seconds, outcome in number of repetitions completed. |
| Secondary | Functional Reach Test | baseline, 6 weeks and 6 months | Participant stand with their feet together and legs straight, then try to reach forward as far as possible, outcome in reach distance (centimeter). |
| Secondary | Timed Up and Go Test | baseline, 6 weeks and 6 months | Participant started in seated position, on instruction would stand up, walk forward for three meters, return back to the chair and sit down. Outcome in time (seconds) needed to complete. |
| Secondary | Knee Society Score (KSS) | baseline, 6 weeks and 6 months | Physician assessed questionnaire measuring patient pain, range of motion, stability, and joint alignment, scoring between 0 to 100, with 100 being perfect score. |
| Secondary | Knee Society Functional Score | baseline, 6 weeks and 6 months | Patient self-assessment questionnaire measuring their ability to execute physical activities, scoring between 0 to 100, with 100 being perfect score. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Source
- Release
- trials-2026-11-12-0.4.0
- Release manifest SHA-256
- 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
- Registry capture
- 2026-11-12
- Results copy, AACT
- 2026-03-23
- NIH clinical studies file
- 2026-11-13
Source ClinicalTrials.gov
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNone stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07912333
GET https://conductscience.org/api/trials/v1/NCT07912333/registered