Deglutition Disorders
Conditions
Interventions
This is a feasibility study designed as a case series and linked to the parent project registered under Brazilian Registry of Clinical Trials (ReBEC - RBR-5s76ksq). This derivative study will be condu
Sponsors
Centro de Ciências da Saúde
Universidade Federal do Espírito Santo
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Eligibility criteria include adults (=18 years) with a confirmed neurological diagnosis and clinical signs or symptoms of swallowing disorders
Exclusion criteria
Exclusion criteria: Patients receiving alternative feeding methods (e.g., enteral tube feeding or gastrostomy) and those with intracranial metallic implants or cardiac pacemakers will be excluded
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| An improvement in swallowing function is expected, as assessed by a decrease in the degree of impairment | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected that there will be less impact on the patient's quality of life related to swallowing | — |
Countries
Brazil
Contacts
Public ContactCarolina Comarela
Universidade Federal do Espírito Santo
Outcome results
None listed