Trial · NCT07902505
Comparison of Telerehabilitation and Usual Rehabilitation After Knee or Hip Surgery
NCT07902505, Not applicable, Not yet recruiting, Centre Hospitalier de Valenciennes
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Comparison of Telerehabilitation and Usual Rehabilitation After Knee or Hip Surgery. Trials, record NCT07902505. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07902505
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Comparison of Telerehabilitation and Usual Rehabilitation After Knee or Hip Surgery
- NCT number
- NCT07902505
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 216 participants, estimated
- Lead sponsor
- Centre Hospitalier de Valenciennes
- Conditions
- Orthopedic Surgery, Rehabilitation
- Interventions
- Standard Inpatient Rehabilitation, Telerehabilitation
- First posted
- 2026-10-29
- Last updated
- 2026-10-29
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Total WOMAC Score at 6 Weeks Postoperatively | 6 weeks postoperatively | Comparison of the total Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) score between the telerehabilitation group and the conventional rehabilitation group at 6 weeks after surgery. |
| Secondary | WOMAC Subscale Scores | Baseline (inclusion), 6 weeks, and 3 months postoperatively | Comparison of changes in the WOMAC pain, stiffness, and physical function subscale scores between the telerehabilitation and conventional rehabilitation groups. |
| Secondary | Changes in KOOS or HOOS Scores | Baseline (inclusion), 6 weeks, and 3 months postoperatively | Comparison of changes in the Knee injury and Osteoarthritis Outcome Score (KOOS) in participants undergoing total knee arthroplasty or the Hip disability and Osteoarthritis Outcome Score (HOOS) in participants undergoing total hip arthroplasty, between the telerehabilitation and conventional rehabilitation groups. |
| Secondary | Changes in EMAPS Questionnaire Score | Baseline (inclusion), 6 weeks, and 3 months postoperatively | Comparison of changes in the EMAPS questionnaire score between the telerehabilitation and conventional rehabilitation groups to assess patient motivation toward rehabilitation and physical activity |
| Secondary | Changes in SF-12 Health Survey Scores | Baseline (inclusion), 6 weeks, and 3 months postoperatively | Comparison of changes in the 12-Item Short Form Health Survey (SF-12) physical and mental component scores between the telerehabilitation and conventional rehabilitation groups |
| Other | Change in Average Daily Step Count Over Time | Baseline, 6 weeks, and 3 months postoperatively. | Evolution of mean daily step count measured using a connected digital device in participants receiving telerehabilitation after total knee or total hip arthroplasty. Changes between measurement time points will be analyzed within the telerehabilitation group. |
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.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license 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/NCT07902505
GET https://conductscience.org/api/trials/v1/NCT07902505/registered