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Evaluation of Oral Screen Training With IQoro as Treatment for Dysphagia After Stroke

Stroke Clinical Trial

Official title:
Evaluation of Oral Screen Training With IQoro as Treatment for Dysphagia After Stroke

Clinical Trial Summary

Purpose The purpose of the study is to evaluate if training with oral screen IQoro® improves swallowing in patients with dysphagia after stroke. Method Inpatient from a stroke unit in Sweden who have been assessed with fiberoptic endoscopic evaluation of swallowing(FEES) which proves swallowing difficulties (dysphagia) were recruited. The participants were randomise to control- or intervention group. Both groups received usual care. The intervention group were instructed to oral screen (IQoro®) training for 13 weeks. Follow up with FEES was made 13 weeks post of recruitment. The assess with FEES was recorded and the recordings are going to be analyzed afterwards to compare the swallowing ability between baseline and follow up in group and between group.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04868955
Study type Interventional
Source Ostergotland County Council, Sweden
Contact
Status Active, not recruiting
Phase N/A
Start date April 26, 2019
Completion date May 3, 2021
View Details
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