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NCT04364490: Copernicus
Rehabilitative Efficacy of a Visual Feedback Device for Locomotion of Post-stroke Patients
NA trial testing Copernicus noVF in Stroke in 162 participants. Completed in 1 December 2019.
31 December 2018
Quick facts
| Lead sponsor | S.Anna Rehabilitation Institute |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 162 |
| Start date | 1 June 2018 |
| Primary completion | 31 December 2018 |
| Estimated completion | 1 December 2019 |
| Sites | 1 location across Italy |
Drugs / interventions tested
- Copernicus noVF
- Copernicis VF-Plus
- Control group — full drug profile →
Conditions studied
- Stroke — all drugs for Stroke →
Sponsor
S.Anna Rehabilitation Institute
Who can join
Adults 35 to 80, any sex, with Stroke. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
We tested the feasibility and efficacy of a novel body-weight support (BWS) gait training system with visual feedback, called Copernicus®. This computerized device provides highly comfortable, regular and repeatable locomotion in hemiplegic patients, training the ability to transfer weight loading alternately on both feet through visual real-time monitoring of gait parameters.
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 NCT04364490
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Other S.Anna Rehabilitation Institute trials
Trials by the same sponsor.
- NCT05288270 — ROBOtic Care of Post-stroke Pain. · NA · unknown
- NCT04321889 — Efficacy of Defurocumarinized Bergamot in the Treatment of Agitation in Severe Dementia Patients. · NA · unknown
- NCT04909658 — The Effect of Acceptance and Commitment Therapy · 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 NCT04364490 (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 S.Anna Rehabilitation Institute
- Last refreshed: 28 April 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/NCT04364490.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing