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Exercise for Swallowing Problems After Stroke

Primary Purpose

Cerebrovascular Accident, Deglutition Disorders

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
lingual press
effortful swallowing
natural swallowing
non-oral sham (control) exercise
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cerebrovascular Accident focused on measuring tongue, pressure

Eligibility Criteria

45 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 3 months post ischemic or hemorrhagic stroke
  • 45 years of age or older
  • physician approval of medical stability
  • aspiration or penetration of the laryngeal vestibule (score of 3 or higher on Penetration/Aspiration Scale) or post swallow residue in the oropharynx
  • able to manage own secretions with no signs of aspiration
  • the capacity to provide informed consent

Exclusion Criteria:

  • neurologic insult (other than stroke) or neuromuscular disease
  • history of radiation to the head or neck
  • poorly controlled psychosis
  • lack the capacity to complete the exercise program
  • refractory alcoholism (on AWD precautions)
  • class IV congestive heart failure
  • sever chronic obstructive pulmonary disease (home oxygen dependent)
  • end-stage renal failure
  • allergy to barium (used in radiographic swallowing assessment

Subjects with known contraindication will be excluded from the MRI portion of the protocol:

  • Cardiac pacemakers
  • Aneurysm clips
  • Neurostimulators
  • Cochlear implant
  • Ossicular prostheses
  • Intracranial or intraorbital foreign bodies
  • Claustrophobia

Sites / Locations

  • Wlliam S. Middleton Memorial Veterans Hospital, Madison

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Sham Comparator

Arm Label

Arm 1

Arm 2

Arm 3

Arm 4

Arm Description

lingual press (high-intensity, oral, non-swallowing)

effortful swallowing (high-intensity swallowing)

natural swallowing (high frequency, low intensity swallowing)

non-oral sham (control) exercise

Outcomes

Primary Outcome Measures

Isometric Lingual Pressure
Tongue Strength
Maximum Isometric Tongue Pressure
Peak isometric pressure at 4 sensors

Secondary Outcome Measures

Full Information

First Posted
July 23, 2008
Last Updated
March 12, 2018
Sponsor
VA Office of Research and Development
Collaborators
University of Wisconsin, Madison
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1. Study Identification

Unique Protocol Identification Number
NCT00722111
Brief Title
Exercise for Swallowing Problems After Stroke
Official Title
Rehabilitation Exercise for Dysphagia Subsequent to Stroke
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Completed
Study Start Date
February 2011 (undefined)
Primary Completion Date
December 2011 (Actual)
Study Completion Date
June 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development
Collaborators
University of Wisconsin, Madison

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether stroke patients with swallowing problems will show greater swallowing improvement with intense oral exercise than subjects who perform either a low intensity oral exercise or a sham exercise.
Detailed Description
Swallowing problems affect as many as 40% of adults over age 60. Serious consequences are suffered by the numerous patients with neuromuscular deficits secondary to stroke. Patients with dysphagia subsequent to stroke face risk of death from pneumonia, perhaps the most serious sequelae of dysphagia, with malnutrition and dehydration also dire secondary consequences. If stroke patients survive, they require longer hospital stays and nursing home placements with diminished rehabilitation potential. Despite these devastating influences that dysphagia secondary to stroke has on health, evidence supporting the effects of specific interventions on swallowing outcomes in this population is sparse. Neural plasticity is the mechanism by which the damaged brain relearns "lost behavior" in response to rehabilitation. A goal of this proposal is to implement several principles of exercise and neural plasticity (specificity, repetition, and intensity) in a clinically justifiable manner so they may be used to guide clinical research and ultimately practice. To that end, we will determine how neuromuscular changes affect swallowing outcomes in response to 3 unique 8-week exercise interventions compared with a sham hand (control) exercise group. The main hypothesis is that after 8 weeks of intense progressive rehabilitation exercise with feedback - lingual press (high-intensity, oral, non-swallowing) stroke patients with dysphagia will show swallowing improvement (defined as an improved score on the Penetration/Aspiration Scale and/or the Residue Scale in the absence of worsening in the other average score) to a greater extent than subjects who perform natural swallowing (low-intensity swallowing) exercises or the sham (control) exercise group. This hypothesis will be tested by 3 discrete objectives: Objective 1: Compare outcomes of four different 8-week exercise interventions among dysphagic stroke patients; Objective 2: Characterize bolus flow, swallowing biomechanics, lingual anatomy and swallowing function of stroke patients through initial calculation of multi-dimensional swallowing profiles pre-intervention and comparison of these profiles post-intervention; and Objective 3: Determine the most appropriate dose of treatment between 4 and 8 weeks for study subjects. We will randomize 200 men and women post-stroke into four groups (50 subjects per group). Subjects will be randomized into one of four groups, to identify treatment outcomes. The exercise interventions include (a) lingual press (high-intensity, oral, non-swallowing) (b) effortful swallowing (high-intensity swallowing); and (c) natural swallowing (low intensity swallowing), compared with (d) a non-oral sham (control) exercise. All exercises will involve 2 sets of 10 repetitions performed 3 times a day on 3 non-consecutive days per week. For Objectives 1 and 2 at baseline, week 4, and week 8, each subject will complete simultaneous videofluoroscopic and lingual pressure measures to calculate measures of bolus flow and swallowing biomechanics, which comprise 1) direction (average Penetration/Aspiration Scale Score), completeness (average Residue Scale Score), and duration in msec; 2) isometric and swallowing pressures; and 3) duration and extent of hyolaryngeal excursion and opening of the upper esophageal sphincter. At each of the 3 timepoints, each subject also will complete magnetic resonance imaging (MRI) to measure stroke lesion volume, lingual volume, and lingual tissue differentiation as well as complete swallowing-specific quality of life and dietary questionnaires. For Objective 3, subjects will complete all measures at baseline and weeks 4 and 8 to determine when the most benefits are made during the course of exercise. Knowledge of the dose response will allow for more accurate prescription of the clinical programs. The Dept. of Veterans Affairs has designated "aging" and its impact on health as high research priorities. As the aging veteran population grows, dysphagia and its deleterious health consequences including pneumonia and/or malnutrition will be an increasing public health burden. In fact, VHA Directive 2006-32 was recently issued (May 17, 2006) defining standard procedures for assessment and treatment of patients with dysphagia. Appropriate diagnosis and treatment for dysphagia with low-cost, non-invasive efficacious exercise programs may not only reduce health care costs, but also will lead to improvements in patient health and quality of life. For patients post-stroke, the implications are enormous when the life-threatening incidence of aspiration is reduced or prevented.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebrovascular Accident, Deglutition Disorders
Keywords
tongue, pressure

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
83 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm 1
Arm Type
Experimental
Arm Description
lingual press (high-intensity, oral, non-swallowing)
Arm Title
Arm 2
Arm Type
Experimental
Arm Description
effortful swallowing (high-intensity swallowing)
Arm Title
Arm 3
Arm Type
Experimental
Arm Description
natural swallowing (high frequency, low intensity swallowing)
Arm Title
Arm 4
Arm Type
Sham Comparator
Arm Description
non-oral sham (control) exercise
Intervention Type
Device
Intervention Name(s)
lingual press
Intervention Description
lingual press (high-intensity, oral, non-swallowing)
Intervention Type
Behavioral
Intervention Name(s)
effortful swallowing
Intervention Description
effortful swallowing (high-intensity swallowing)
Intervention Type
Behavioral
Intervention Name(s)
natural swallowing
Intervention Description
natural swallowing (high frequency, low intensity swallowing)
Intervention Type
Behavioral
Intervention Name(s)
non-oral sham (control) exercise
Intervention Description
non-oral sham (control) exercise
Primary Outcome Measure Information:
Title
Isometric Lingual Pressure
Description
Tongue Strength
Time Frame
8 weeks
Title
Maximum Isometric Tongue Pressure
Description
Peak isometric pressure at 4 sensors
Time Frame
16 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 3 months post ischemic or hemorrhagic stroke 45 years of age or older physician approval of medical stability aspiration or penetration of the laryngeal vestibule (score of 3 or higher on Penetration/Aspiration Scale) or post swallow residue in the oropharynx able to manage own secretions with no signs of aspiration the capacity to provide informed consent Exclusion Criteria: neurologic insult (other than stroke) or neuromuscular disease history of radiation to the head or neck poorly controlled psychosis lack the capacity to complete the exercise program refractory alcoholism (on AWD precautions) class IV congestive heart failure sever chronic obstructive pulmonary disease (home oxygen dependent) end-stage renal failure allergy to barium (used in radiographic swallowing assessment Subjects with known contraindication will be excluded from the MRI portion of the protocol: Cardiac pacemakers Aneurysm clips Neurostimulators Cochlear implant Ossicular prostheses Intracranial or intraorbital foreign bodies Claustrophobia
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
JoAnne Robbins, PhD
Organizational Affiliation
Wlliam S. Middleton Memorial Veterans Hospital, Madison
Official's Role
Principal Investigator
Facility Information:
Facility Name
Wlliam S. Middleton Memorial Veterans Hospital, Madison
City
Madison
State/Province
Wisconsin
ZIP/Postal Code
53705
Country
United States

12. IPD Sharing Statement

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Exercise for Swallowing Problems After Stroke

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