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Clinical Trials/NCT04402307
NCT04402307CompletedNot Applicable

Effect of Training of Patients With Dysphagia

Vendsyssel Hospital16 sites in 1 country93 target enrollmentStarted: March 25, 2019Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
93
Locations
16
Primary Endpoint
Readmission
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

Effect of training of patients with dysphagia

Detailed Description

A randomised controlled study in the effect of training in patients with dysphagia.

The patients are randomised for training or for usual care.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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

Outcomes

Primary Outcomes

Readmission

Time Frame: 6 months

Number of readmissions within 6 months

Secondary Outcomes

  • Change in Quality of life(3 months)
  • Cost effectiveness(6 months)
  • Swallowing function(3 months)
  • Mortality(6 months)

Investigators

Sponsor
Vendsyssel Hospital
Sponsor Class
Other Gov
Responsible Party
Principal Investigator
Principal Investigator

Dorte Melgaard Kristiansen

Seniorresearcher, research coordinator, ph.d.

Vendsyssel Hospital

Study Sites (16)

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