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Benefits of Using a Transparent Visor to Replace the Face Mask in Speech Therapy Rehabilitation of Oral-Linguo-Facial Praxies in the Context of COVID-19: a Series of Cases

Benefits of Using a Transparent Visor to Replace the Face Mask in Speech Therapy Rehabilitation of Oral-Linguo-Facial Praxies in the Context of COVID-19: a Series of Cases

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04639427
Acronym
Co-VIS
Enrollment
4
Registered
2020-11-20
Start date
2021-02-08
Completion date
2021-07-31
Last updated
2021-07-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid19, Oral-Linguo-Facial Praxies

Keywords

Oral-Linguo-Facial praxies, Covid19, speech therapy rehabilitation

Brief summary

The primary objective of the study is to compare the effectiveness of the use of a transparent covering visor with that of the face mask, with or without the use of video sequences, for speech therapy rehabilitation of oral-linguo-facial praxies in the context of the COVID 19 epidemic.

Detailed description

Statistic analysis: single case experimental design (SCED) method.

Interventions

None listed

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Aged \>= 18 years; * Hospitalization for more than 2 weeks prior to enrollment in the adult post intensive care rehabilitation care unit (PICRU) of Raymond Poincaré hospital in Garches; * With oral-linguo-facial praxis disorders whatever the cause; * Has been informed and not in opposition to participation of the study.

Exclusion criteria

* Patient with fever or any suspect symptom of a SARS-CoV2 infection; * Planned discharge of hospital in 2 weeks; * Patient with cognitive, phasic or vigilance disorders preventing to understand the study; * Under guardianship or curator; * Patient Under french AME scheme.

Design outcomes

Primary

MeasureTime frame
Oral-Linguo-Facial Motricity Testthroughtout of the study, an average of 2 weeks

Countries

France

Contacts

Primary ContactJulie PAQUEREAU, MD
julie.paquereau@aphp.fr+ 33 (0)1 47 10 79 00

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026