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

NCT04868955 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2021-05-03

No results posted yet for this study

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.

Conditions

Interventions

OTHER

Oral screen training

Oral screen training (IQoro®) during 13 weeks.

Sponsors & Collaborators

  • Rebecca Norrman and Elin Rova

    lead OTHER

Principal Investigators

  • Rebecca U Norrman, Master · Ostergotland County Council, Sweden

  • Elin AM Rova, Master · Ostergotland County Council, Sweden

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-04-26
Primary Completion
2021-05-03
Completion
2021-05-03

Countries

  • Sweden

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04868955 on ClinicalTrials.gov