QUESST: Innovative Measures of Speech and Swallowing Dysfunction in Neurological Disorders

Sponsor
Beth Israel Deaconess Medical Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT02118805
Collaborator
(none)
200
1
159
1.3

Study Details

Study Description

Brief Summary

This study is evaluating the use of two painless, non-invasive technologies in the assessment of muscle health over time in both healthy volunteers and patients who have diseases that affect the nervous system.

Detailed Description

Speech and swallowing abnormalities are important symptoms associated with disorders of the central nervous system, motor neuron disease (such as amyotrophic lateral sclerosis), myasthenia gravis, and primary muscle conditions. In addition to characterizing the evolution in muscle architecture that could underlie associated orofacial weakness, identifying new ways to measure these abnormalities is critical to the development and testing of novel treatment approaches. As painless, non-invasive, portable technologies, quantitative ultrasonography (QUS) and electrical impedance myography (EIM) could meet the need for objective measures of speech and swallowing dysfunction.

In QUS, acoustic energy is applied to a muscle of interest; the resultant pictorial data are translated into a single value that reflects the health of the imaged muscle. Similarly, in EIM, a high-frequency, low-intensity alternating electrical current is applied to individual muscles, and the resulting voltages measured. Impedance values reflect changes in muscle architecture, including fiber atrophy, inflammation, and the replacement of muscle with fat or connective tissue. Both of these user-friendly methods can provide sensitive indicators of neuromuscular disease status when applied to the limbs. Although they have also been used to evaluate orofacial muscles in healthy volunteers and patients with primary muscle disorders, they have not yet been systematically studied in patients with a range of neurological conditions.

When applied to muscles of the face and tongue, such tools could 1. Improve accuracy of early diagnosis; 2. Allow monitoring of speech and swallowing dysfunction over time; 3. Help individualize care; and 4. Serve as biomarkers in clinical trials. We propose that QUS and EIM will provide convenient, reliable, clinically meaningful surrogate markers of orofacial dysfunction in a variety of neurologic conditions.

Study Design

Study Type:
Observational
Anticipated Enrollment :
200 participants
Observational Model:
Other
Time Perspective:
Cross-Sectional
Official Title:
Quantitative Ultrasonography and Electrical Impedance Myography: Speech and Swallowing Technologies for Use in Neurological Disorders
Study Start Date :
Oct 1, 2013
Anticipated Primary Completion Date :
Dec 31, 2025
Anticipated Study Completion Date :
Dec 31, 2026

Arms and Interventions

Arm Intervention/Treatment
Patients with ALS

No intervention is used in this study. The health of muscle is monitored over time.

Patients with Myasthenia Gravis

No intervention is used in this study. The health of muscle is monitored over time.

Patients with Muscle Disease

No intervention is used in this study. The health of muscle is monitored over time.

Patients with Stroke

No intervention is used in this study. The health of muscle is monitored over time.

Patients with Parkinson's Disease

No intervention is used in this study. The health of muscle is monitored over time.

Healthy Volunteers

No intervention is used in this study. The health of muscle is monitored over time.

Outcome Measures

Primary Outcome Measures

  1. Change in Muscle Health over 18 months by Standard Ultrasound [Baseline, Month 3, Month 6, Month 9, Month 12, Month 15, and Month 18]

    Selected muscles of the face, limbs, trunk, and tongue will be visualized with painless, non-invasive ultrasound; this measure will be performed in healthy volunteers and participants with neurological conditions

Secondary Outcome Measures

  1. Change in Score on the Sydney Swallow Questionnaire (over 18 months) [Baseline, Month 3, Month 6, Month 9, Month 12, Month 15, and Month 18]

    Participants with neurological conditions will answer questions about swallowing

  2. Change in Number of Seconds It takes to Repeat Individual Words Ten Times (over 18 months) [Baseline, Month 3, Month 6, Month 9, Month 12, Month 15, and Month 18]

    Participants with neurological conditions will be asked to repeat "pepper" and "ticker" ten times as quickly as possible

  3. Change in Number of Seconds It Takes to Swallow of 3 ounces of Water (over 18 months) [Baseline, Month 3, Month 6, Month 9, Month 12, Month 15, and Month 18]

    Participants with neurological conditions will be asked to perform this task if safe

  4. Change in Score on the Amyotrophic Lateral Sclerosis Rating Scale - Revised (ALSFRS-R) (over 18 months) [Baseline, Month 3, Month 6, Month 9, Month 12, Month 15, and Month 18]

    Participants who have been diagnosed with ALS will answer questions about function, including speech and swallowing

  5. Change in Score on the Quantitative Myasthenia Gravis Scale (over 18 months) [Baseline, Month 3, Month 6, Month 9, Month 12, Month 15, and Month 18]

    Participants who have been diagnosed with Myasthenia Gravis will be asked to perform certain tasks, such as raising the arm, and the findings will be scored by a research team member

  6. Change in Score on the United Parkinson's Disease Rating Scale (UPDRS) (over 18 months) [Baseline, Month 3, Month 6, Month 9, Month 12, Month 15, and Month 18]

    Participants who have been diagnosed with Parkinson's Disease will be asked questions about function, including speech and swallowing

  7. Change in Muscle Health by Standard Concentric Needle Electromyography (EMG) (over 18 months) [Baseline, Month 3, Month 6, Month 9, Month 12, Month 15, and Month 18]

    Participants who have been diagnosed with ALS will be asked if they are willing to participate in standard needle EMG of selected muscles of the face and tongue

  8. Change in Muscle Health by Specialized Electrical Impedance Arrays [Baseline, Month 3, Month 6, Month 9, Month 12, Month 15, and Month 18]

    Selected muscles of the face, limbs, trunk, and tongue will be measured using painless, specialized electrode arrays; this measure will be performed in healthy volunteers and participants with neurological conditions

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Established, or clinically probable, neurologic diagnosis with at least the potential for associated bulbar dysfunction

  • Age 20-90 years

Exclusion Criteria:
  • History or presence of a medical condition that substantially impacts bulbar function

  • Age under 20 or over 90 years

Contacts and Locations

Locations

Site City State Country Postal Code
1 Beth Israel Deaconess Medical Center Boston Massachusetts United States 02215

Sponsors and Collaborators

  • Beth Israel Deaconess Medical Center

Investigators

  • Principal Investigator: Seward Rutkove, MD, Beth Israel Deaconess Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Seward Rutkove, Professor of Neurology, Beth Israel Deaconess Medical Center
ClinicalTrials.gov Identifier:
NCT02118805
Other Study ID Numbers:
  • 2013P000204
First Posted:
Apr 21, 2014
Last Update Posted:
Mar 11, 2022
Last Verified:
Mar 1, 2022

Study Results

No Results Posted as of Mar 11, 2022