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Clinical Trials/NCT01418105
NCT01418105
Completed
Phase 1

Dysphagia and Cervical Spine Disorders in Patients With Neurologic Deficits Due to Brain Lesions

University of Ioannina1 site in 1 country70 target enrollmentJanuary 2011

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Prevention
Sponsor
University of Ioannina
Enrollment
70
Locations
1
Primary Endpoint
change of swallowing ability by Okuma's questionnaire
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The research is about a prospective study conducted in patients suffering from dysphagia and cervical spine disorders and how they are interrelated. Three questionnaires have been given to patients with neurologic deficits, the first of these investigates the occurence of dysphagia in the three stages of swallowing, the second looks into the quality of life following a stroke or other neurologic damage and the third analyses how cervical spine disorders can affect every day life. After the bedside examination, VFSS or FEES, the patients are submitted to swallowing and cervical resistance exercises in fixed time periods after their hospitalisation. The results will be collected and evaluated using the statistical programme SPSS.

Registry
clinicaltrials.gov
Start Date
January 2011
End Date
October 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Avraam Ploumis

Assistant Professor of PMR, Orthopaedic Spine Surgeon

University of Ioannina

Eligibility Criteria

Inclusion Criteria

  • brain lesions and cervical spine disorders

Exclusion Criteria

  • peripheral damages

Outcomes

Primary Outcomes

change of swallowing ability by Okuma's questionnaire

Time Frame: at the time of admittance to the rehabilitation department (baseline), at six weeks, at one year

change of cervical scoliosis measured by Cobb method in x-rays

Time Frame: at the time of admittance to the rehabilitation department (baseline), at six weeks, at one year

change in swallowing ability and quality of life by swal-quol questionnaire

Time Frame: at the time of admittance to the rehabilitation department (baseline), at six weeks, at one year

Secondary Outcomes

  • change of cervical oswestry disability index(at the time of admittance to the rehabilitation department (baseline), at six weeks, at one year)

Study Sites (1)

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