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NCT05902091
Neurophysiology-based Intervention of Foot Dysfunction in Sportive Children
NA trial testing Neurophysiology-based intervention in Flatfoot, Flexible in 14 participants. Completed in 20 September 2018.
5 September 2017
Quick facts
| Lead sponsor | Charles University, Czech Republic |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 14 |
| Start date | 10 June 2016 |
| Primary completion | 5 September 2017 |
| Estimated completion | 20 September 2018 |
| Sites | 1 location across Czechia |
Drugs / interventions tested
- Neurophysiology-based intervention
Conditions studied
- Flatfoot, Flexible — all drugs for Flatfoot, Flexible →
- Sports Physical Therapy — all drugs for Sports Physical Therapy →
- Child Development — all drugs for Child Development →
Sponsor
Charles University, Czech Republic
Who can join
Adults 9 to 10, male only, with Flatfoot, Flexible or Sports Physical Therapy. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The goal of the clinical trial study is to test the effect of the individual complex physiotherapy intervention program in the children actively playing soccer with flatfoot or valgus foot. The aims are: 1. see if the medial longitudinal arch will by actively more higher after the intervention 2. see if the type of the foot will change toward more neutral type after the intervention 3. see if the transfer of the centre of body mass through the foot during the gait will directed in more neutral line after the intervention The participants will undergo clinical assessment of short kinesiology assessment visually in underwear and barefoot. Then Participant will be tested for balance test in narrow stance with open and closed eyes, and single.leg stance with open eyes on the pressure mat. Finally, participant will walking in self-selected normal speed through the gait pressure mat. Eaxh procedure will be measured twice, before the program start and after the 4 weeks when the program finish. Researchers will compare these two measurement for the changes.
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 NCT05902091
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Charles University, Czech Republic trials
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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 NCT05902091 (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 Charles University, Czech Republic
- Last refreshed: 13 June 2023
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/NCT05902091.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing