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Expiratory Muscle Training for Persons With Neurodegenerative Disease (EMST)

Primary Purpose

Parkinson's Disease, Multiple Sclerosis

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
EMST
Sham
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 Parkinson's Disease focused on measuring Multiple Sclerosis, Parkinson's disease, Dysphagia

Eligibility Criteria

35 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Multiple Sclerosis Participants
  • Diagnosis of primary, secondary, or relapsing-remitting MS by a neurologist
  • Over 85% of the patient populations that come from the study sites demonstrate relapsing-remitting MS with an average relapse frequency of once every 3 years

Parkinson's Disease Participants

  • Hoehn & Yahr, stage II and III as indicated by certified movement disorders neurologist

All Participants

  • Between 35 and 80 years of age
  • Non-smoking or no smoking within the previous five years
  • No history of head and neck cancer, asthma or COPD, untreated hypertension
  • Sufficient facial muscle strength so as to achieve and maintain adequate lip closure around a circular mouthpiece
  • Cognition within normal limits as determined by the: Mini Mental Status Exam (MMSE; 1975No neurological (other than MS or PD) condition which adversely affects respiratory muscle or gas exchange system
  • Reduced MEP's compared to published normative data for age and sex
  • Reduced expiratory peak flow rates (6-8 L/s for young to middle age adults and 3.6 L/s for 65 and older) during voluntary cough production for age and sex (Bolser, personal communication; Smith-Hammond & Goldstein, 2006)
  • Participant report of symptoms related to swallow impairment

Exclusion Criteria:

  • DBS
  • COPD
  • Asthma
  • Smoking or smoking within preceding 5 years

Sites / Locations

  • North Florida/South Georgia Veterans Health System, Gainesville, FL

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

Arm 1: EMST

Arm 2: Sham group

Arm Description

The experimental group receives five weeks of expiratory muscle strength training (EMST) using a positive pressure threshold device

The Sham group undergoes the same 5-week EMST exercise as the experimental group using the same device but without a spring for minimal pressure load

Outcomes

Primary Outcome Measures

Maximum Expiratory Pressure (MEP)
Expiratory pressure generating capacity assessed via handheld manometer.
Penetration-Aspiration Scale Score
The Penetration-Aspiration Scale (PAS) was used to measure swallow safety. PAS is an 8 point ordinal scale for quantification of penetration and aspiration. PAS measures the depth to which material enters the airway and if the material is expelled following penetration or aspiration. Categorical groupings of PAS scores include "normal to mild" (1-2), "moderate" (3-5) and "severe" (6-8, indicating that material has passed into the lower airway). These PAS scores may be useful in denoting clinically significant changes (e.g. moderate to mild) resulting from treatment or disease progression. The following table reports the percentage of participants (out of the respective total group participants in EMST and Sham) with changed PAS score of 1 point or more (improving or worsening) and without PAS score changes from pre- to post treatment. The data represent an exploratory quantification without statistical analysis.
Swallow-related Quality of Life (SWAL-QOL)
The SWAL-QOL is a validated and standardized tool that measures burden; symptom status including pharyngeal, oral, and saliva; fear; and mental health subdomains. Responses are determined according to an ordinal scale where 1 equals a severe problem and 5 equals no problem. The SWAL-QOL provides an overall score as well as subscale scores. Subjects rate quality of life as follows (expressed as percentage of the possible perfect score): little to no impact (81% - 100%), mild impact (61% - 80%), moderate impact (41% - 60%), severe impact (21% - 40%), and profound impact (0% - 20%).

Secondary Outcome Measures

Full Information

First Posted
March 3, 2009
Last Updated
December 19, 2016
Sponsor
VA Office of Research and Development
Collaborators
University of Florida
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1. Study Identification

Unique Protocol Identification Number
NCT00856518
Brief Title
Expiratory Muscle Training for Persons With Neurodegenerative Disease
Acronym
EMST
Official Title
Expiratory Muscle Training for Persons With Neurodegenerative Disease
Study Type
Interventional

2. Study Status

Record Verification Date
December 2016
Overall Recruitment Status
Completed
Study Start Date
March 2009 (undefined)
Primary Completion Date
August 2014 (Actual)
Study Completion Date
August 2014 (Actual)

3. Sponsor/Collaborators

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

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Respiratory difficulty is one of the primary factors leading to death in patients with Parkinson's Disease (PD) and Multiple Sclerosis. Both diseases are progressive degenerating diseases that cause difficulties in breathing, airway protection and swallowing. Patients with PD and MS typically become sedentary and lose endurance, maximal fitness levels and overall pulmonary function. Much of the research focus has been on the motor symptoms of PD and MS yet the pulmonary and swallowing complications are perhaps ultimately the most important disability as the diseases progress. The inability to generate adequate respiratory pressure is responsible for reduced cough magnitudes and cough response times. Cough is critical for the clearance of foreign materials in the airway helping to reduce infiltration of bacteria and subsequent respiratory infection. With reduced cough function an increased risk for pulmonary disease occurs due to a reduced ability to protect the airways. There are a number of promising outcomes from an expiratory strength-training program. By increasing expiratory muscle strength and expiratory pressure generation, effective breathing, clearance of the airway, and improved swallowing can occur. These explicit outcomes are predicted based on our experience with the use of an innovative device-driven, home-based expiratory strength training program focused on the expiratory muscles of respiration. This project focuses on following patients with PD and MS for an initial 5 weeks of strength training and them testing the outcome of a caregiver program for maintaining treatment effects.
Detailed Description
The proposed investigation will: Determine if 5 weeks of Expiratory Muscle Strength Training (EMST) increases maximal expiratory driving pressure (MEP) and improves swallow, cough and breathing function in individuals with PD and MS. Following the post assessment of the 5 week EMST program we will then evaluate three different modules for monitoring the continuation of the treatment while assessing patient quality of life and caregiver burden/satisfaction. This will help us determine if one particular home training method results in different physiological and functional outcomes. Aim 1. Determine the effects of an EMST program on swallow function, voluntary cough production and breathing function in individuals with PD and MS identified as below normal limits for their age and sex (via physiological measures). Hypothesis 1: There will significant and positive treatment effects following 5 weeks of EMST on the measures of swallow, cough production and breathing function in those with PD and MS following 5 weeks of treatment. Aim 2: Determine the outcome of three uniquely structured home treatment monitoring programs in maintaining the EMST post treatment effect for patients with MS and PD. These programs are referred to as: Education Module (A), Question Only (B), and Education Module plus Question (C). The monitoring system will be provided by VitelNet, a leading provider of home health monitoring, clinician-based telemedicine Hypothesis 2: Program C will provide greater maintenance of the EMST treatment effect for both patient groups compared to programs A and B. Aim 3: Determine the effects of the home monitoring programs for improving patient quality of life and caregiver burden/satisfaction. Hypothesis 3: Program C will provide greater improvements in patient quality of life and caregiver burden compared to programs A and B.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson's Disease, Multiple Sclerosis
Keywords
Multiple Sclerosis, Parkinson's disease, Dysphagia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
42 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm 1: EMST
Arm Type
Active Comparator
Arm Description
The experimental group receives five weeks of expiratory muscle strength training (EMST) using a positive pressure threshold device
Arm Title
Arm 2: Sham group
Arm Type
Sham Comparator
Arm Description
The Sham group undergoes the same 5-week EMST exercise as the experimental group using the same device but without a spring for minimal pressure load
Intervention Type
Device
Intervention Name(s)
EMST
Other Intervention Name(s)
EMST 150
Intervention Description
Pressure threshold device (Expiratory Muscle Strength Trainer) targeted at increase muscle force generation of expiratory and submental muscles.
Intervention Type
Device
Intervention Name(s)
Sham
Intervention Description
The same device just like the EMST but does not provide a load on the target muscle group
Primary Outcome Measure Information:
Title
Maximum Expiratory Pressure (MEP)
Description
Expiratory pressure generating capacity assessed via handheld manometer.
Time Frame
at baseline and again after 5-week EMST exercise
Title
Penetration-Aspiration Scale Score
Description
The Penetration-Aspiration Scale (PAS) was used to measure swallow safety. PAS is an 8 point ordinal scale for quantification of penetration and aspiration. PAS measures the depth to which material enters the airway and if the material is expelled following penetration or aspiration. Categorical groupings of PAS scores include "normal to mild" (1-2), "moderate" (3-5) and "severe" (6-8, indicating that material has passed into the lower airway). These PAS scores may be useful in denoting clinically significant changes (e.g. moderate to mild) resulting from treatment or disease progression. The following table reports the percentage of participants (out of the respective total group participants in EMST and Sham) with changed PAS score of 1 point or more (improving or worsening) and without PAS score changes from pre- to post treatment. The data represent an exploratory quantification without statistical analysis.
Time Frame
at baseline and again after 5-week EMST exercise
Title
Swallow-related Quality of Life (SWAL-QOL)
Description
The SWAL-QOL is a validated and standardized tool that measures burden; symptom status including pharyngeal, oral, and saliva; fear; and mental health subdomains. Responses are determined according to an ordinal scale where 1 equals a severe problem and 5 equals no problem. The SWAL-QOL provides an overall score as well as subscale scores. Subjects rate quality of life as follows (expressed as percentage of the possible perfect score): little to no impact (81% - 100%), mild impact (61% - 80%), moderate impact (41% - 60%), severe impact (21% - 40%), and profound impact (0% - 20%).
Time Frame
at baseline and after 5-week of EMST exercise

10. Eligibility

Sex
All
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Multiple Sclerosis Participants Diagnosis of primary, secondary, or relapsing-remitting MS by a neurologist Over 85% of the patient populations that come from the study sites demonstrate relapsing-remitting MS with an average relapse frequency of once every 3 years Parkinson's Disease Participants Hoehn & Yahr, stage II and III as indicated by certified movement disorders neurologist All Participants Between 35 and 80 years of age Non-smoking or no smoking within the previous five years No history of head and neck cancer, asthma or COPD, untreated hypertension Sufficient facial muscle strength so as to achieve and maintain adequate lip closure around a circular mouthpiece Cognition within normal limits as determined by the: Mini Mental Status Exam (MMSE; 1975No neurological (other than MS or PD) condition which adversely affects respiratory muscle or gas exchange system Reduced MEP's compared to published normative data for age and sex Reduced expiratory peak flow rates (6-8 L/s for young to middle age adults and 3.6 L/s for 65 and older) during voluntary cough production for age and sex (Bolser, personal communication; Smith-Hammond & Goldstein, 2006) Participant report of symptoms related to swallow impairment Exclusion Criteria: DBS COPD Asthma Smoking or smoking within preceding 5 years
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Janis J. Daly, PhD MS
Organizational Affiliation
North Florida/South Georgia Veterans Health System, Gainesville, FL
Official's Role
Principal Investigator
Facility Information:
Facility Name
North Florida/South Georgia Veterans Health System, Gainesville, FL
City
Gainesville
State/Province
Florida
ZIP/Postal Code
32608
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Expiratory Muscle Training for Persons With Neurodegenerative Disease

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