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NCT03648060
Efficacy of a Digital Biofeedback System for Home-based Rehabilitation After Total Joint Replacement
NA trial testing Digital kinematic biofeedback system in Hip Osteoarthritis in 88 participants. Completed in 15 May 2020.
15 May 2020
Quick facts
| Lead sponsor | Sword Health, SA |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 88 |
| Start date | 8 October 2018 |
| Primary completion | 15 May 2020 |
| Estimated completion | 15 May 2020 |
| Sites | 1 location across Portugal |
Drugs / interventions tested
- Digital kinematic biofeedback system
Conditions studied
- Hip Osteoarthritis — all drugs for Hip Osteoarthritis →
- Knee Osteoarthritis — all drugs for Knee Osteoarthritis →
Sponsor
Sword Health, SA
Who can join
18 and older, any sex, with Hip Osteoarthritis or Knee Osteoarthritis. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The study was designed to assess the efficacy of a home-based rehabilitation program using a digital kinematic biofeedback system after total hip or knee replacement. This is a single-arm prospective study. Patients will be enrolled pre-operatively and will perform an 8-week rehabilitation program starting between day 7 and 10 after surgery. This program will consist of rehabilitation sessions performed independently by the patient at under remote monitoring from a physical therapist. Outcomes will be measured at baseline, 4 weeks into the rehabilitation program and at the end of the program. The primary outcome is the change in patient performance measure through the Timed-up-and-Go (TUG) test in comparison with the pre-operative score. Secondary outcomes will be measured in terms of: a) patient reported outcomes (Hip or Knee Osteoarthritis Outcome Score) and b) range of motion of the relevant joint (hip or knee).
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT03648060
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Currently open trials in the same condition.
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- NCT07327372 — PENG Block With Dexmedetomidine in Older Adults · NA · recruiting
- NCT07347041 — Clinical Study of Myofascial Trigger Points(MTrPs) Injection in the Treatment of Hip Osteoarthritis(OA) · NA · recruiting
Other Sword Health, SA trials
Trials by the same sponsor.
- NCT05417685 — Digital Care Programs for Musculoskeletal Health · enrolling by invitation
- NCT04636528 — Digital Versus Conventional Physical Therapy for Chronic Shoulder Tendinopathy · NA · completed
- NCT04808141 — Digital Care Program for Chronic Low Back Pain · NA · completed
- NCT04401683 — Home-based Exercise Rehabilitation With a Novel Digital Biofeedback System for Chronic Low Back Pain · NA · withdrawn
- NCT04092946 — Digital Home-based Rehabilitation for Musculoskeletal Disorders · NA · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03648060 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Sword Health, SA
- Last refreshed: 22 October 2020
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03648060.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing