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NCT04402307 Clinical Trial

Effect of Training of Patients With Dysphagia

Dysphagia Clinical Trial

Official title:
Effect of Training of Patients With Dysphagia

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04402307
Other study ID # RHN_DMK_05
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 25, 2019
Est. completion date December 31, 2020

Study information
Verified date October 2021
Source Vendsyssel Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Effect of training of patients with dysphagia

Description:

A randomised controlled study in the effect of training in patients with dysphagia. The patients are randomised for training or for usual care.

Recruitment information / eligibility
Status Completed
Enrollment 93
Est. completion date December 31, 2020
Est. primary completion date December 31, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients diagnosed with dysphaigia - Patients living in the participating locations Exclusion Criteria: - Patients who are linguistically or cognitively unable to participate - Patients who are unable to collaborate about the training - Palliative patients - Patients with a probe

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Chin Tuck Against Resistance
Training in 6 weeks 3 times a day.

Locations
Country Name City State
Denmark Brøndby municipality Brøndby
Denmark Jammerbugt municipality Brovst
Denmark Frederikshavn municipality Frederikshavn
Denmark Hjørring municipality Hjørring
Denmark Kolding municipality Kolding
Denmark Odense municipality Odense
Denmark Slagelse municipality Slagelse
Denmark Tønder municipality Tønder

Sponsors (1)
Lead Sponsor Collaborator
Vendsyssel Hospital

Country where clinical trial is conducted

Denmark, 

Outcome
Type Measure Description Time frame Safety issue
Primary Readmission Number of readmissions within 6 months 6 months
Secondary Change in Quality of life Level of quality of life - measured with Dysphagia Handicap Index questionnaire 3 months
Secondary Cost effectiveness Economic evaluation of training compared to usual care, measured with EQ-5D 6 months
Secondary Mortality Mortality in patients with dysphagia within 6 months 6 months
Secondary Swallowing function Aspiration (yes/no) - measured with Volume Viscosity Swallow Test 3 months
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