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Sponsors and Collaborators: |
Royal Perth Hospital Royal Perth Hospital Medical Research Foundation |
Information provided by: | Royal Perth Hospital |
ClinicalTrials.gov Identifier: | NCT00257764 |
Swallowing dysfunction after stroke is common, but there is no reliable evidence for how it should be managed other than perhaps by nasogastric tube. This study compared the effectiveness of standardised, low and high intensity behavioral intervention for dysphagia with that of “usual care”.
Condition | Intervention | Phase |
Dysphagia |
Behavioral: behavioral swallowing exercises/ strategies |
Phase II Phase III |
MedlinePlus related topics: | Swallowing Disorders |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Single Blind, Dose Comparison, Parallel Assignment, Efficacy Study |
Official Title: | A Randomised Controlled Trial of Dysphagia Therapies for Swallowing Disorders Following Stroke. |
Estimated Enrollment: | 300 |
Study Start Date: | May 1996 |
Estimated Study Completion Date: | May 1999 |
Stroke compromises swallowing function, causing dysphagia, in one quarter to one half of all patients. Dysphagia is associated with an increased risk of aspiration pneumonia, dehydration and malnutrition. Despite the development and implementation of several strategies of managing dysphagia after stroke, Few have been evaluated by means of randomised controlled trials.
Comparisons: This study aims to compare stroke patients with dysphagia assigned to receive usual swallowing care, prescribed by the attending physician; standardised low intensity intervention comprising swallowing compensation strategies and diet prescription; or standardised high intensity intervention and dietary prescription .
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Australia, Western Australia | |||||
Royal Perth Hospital | |||||
Perth, Western Australia, Australia, 6000 |
Royal Perth Hospital |
Royal Perth Hospital Medical Research Foundation |
Study Director: | Graeme Hankey, MBBS, MD, | Royal Perth Hospital |
Principal Investigator: | Giselle D Mann, MPH,PhD | Royal Perth Hospital |
Study ID Numbers: | RPH00096 |
First Received: | November 21, 2005 |
Last Updated: | May 4, 2006 |
ClinicalTrials.gov Identifier: | NCT00257764 |
Health Authority: | Australia: National Health and Medical Research Council |
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