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NCT05130736
Rehabilitation Robot in Patients With Post-Coronavirus Disease (COVID-19) Fatigue Syndrome
NA trial testing Robot rehabilitation in Post-Viral Fatigue Syndrome in 80 participants. Status unknown.
31 July 2022
Quick facts
| Lead sponsor | Poznan University of Medical Sciences |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | diagnostic |
| Enrollment | 80 |
| Start date | 1 August 2021 |
| Primary completion | 31 July 2022 |
| Estimated completion | 31 December 2022 |
| Sites | 1 location across Poland |
Drugs / interventions tested
- Robot rehabilitation
Conditions studied
- Post-Viral Fatigue Syndrome — all drugs for Post-Viral Fatigue Syndrome →
Sponsor
Poznan University of Medical Sciences
Who can join
Eligibility, any sex, with Post-Viral Fatigue Syndrome. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The aim of the study is to compare the effectiveness of two models of rehabilitation: * traditional neurological rehabilitation, and * neurological rehabilitation combined with a rehabilitation robot (Luna by EGZOTech). An additional goal is to test the qualitative diagnostic reference using the surface electromyogram of the Luna robot (certified as a Medical Device) for functional diagnostics based on standardized clinical tests.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Application of an EMG-Rehabilitation Robot in Patients with Post-Coronavirus Fatigue Syndrome (COVID-19)-A Feasibility Study.
Zasadzka E, Tobis S, Trzmiel T, Marchewka R, et al · · 2022 · cited 11× · PMID 36012033 · DOI 10.3390/ijerph191610398 -
The Effect of Using a Rehabilitation Robot for Patients with Post-Coronavirus Disease (COVID-19) Fatigue Syndrome.
Trzmiel T, Marchewka R, Pieczyńska A, Zasadzka E, et al · · 2023 · cited 8× · PMID 37836950 · DOI 10.3390/s23198120
Verify or expand the search:
- PubMed search for NCT05130736
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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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 NCT05130736 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Poznan University of Medical Sciences
- Last refreshed: 23 November 2021
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/NCT05130736.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing