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OpenTrials
Completed

NCT Number: NCT04889898

Remote Speech and Swallowing Assessment in ALS

The investigators propose a longitudinal home study of ALS patients to measure the severity of speech and swallowing (bulbar) impairment via a smartphone-based, remote speech and swallow assessment (rSSA). The study is designed to assess the feasibility and validity of such a monitoring intervention. Furthermore, it is proposed that regular monitoring of these two bulbar processes may shed light on their co-evolution over the course of ALS.

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Key information

About this study

Most individuals with ALS experience bulbar function deterioration over the course of the disease which impacts their quality of life significantly. Furthermore, in some patients, bulbar symptoms are an initial presenting symptom of ALS. Identifying these changes, which may be rapid in some individuals, is complicated by the recent acceleration of virtual care delivery.

The investigators propose a longitudinal home study of ALS patients to assess bulbar progression via a smartphone-based, self-administered remote speech and swallow assessment (rSSA). The overall hypothesis is that this monitoring protocol can be used in a way that, 1) is satisfactory to the patient, 2) performs at least as well as standard clinical measures of dysarthria and dysphagia, and 3) resolves the development of emergence of speech and swallowing pathologies in ALS.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Patients

  • At least 18 years of age
  • Possess a diagnosis of ALS (definite, probable, probable laboratory-supported, or possible by El Escorial criteria [35])
  • Have symptom onset within the last 3 years
  • Demonstrate a score of 2 or 3 in either the speech (item #1) or swallowing (item #3) components of the ALSFRS-R at time of enrollment
  • Demonstrate decline in bulbar function prior to enrollment, measured by a reduction of at least 1 point on either the speech or swallowing components of the ALSFRS-R in the 6 months prior to enrollment. If 6 months of data is not available, an estimate of the change in ALSFRS-R will be calculated from the time of symptom onset.
  • Have a life expectancy ≥ 6 months as determined by the attending neurologist
  • Be fluent in written and spoken English
  • Possess a smartphone capable of running the study application
  • Follow up in the Penn State Hershey multidisciplinary ALS clinic over next 6 months
  • Be able to visit the study site for in-person procedures at weeks 0 and 24

Listeners

  • Between 18 and 40 years of age
  • Native speakers of American English 2.3. Currently residing within the United States. 3.4. Hearing within normal limits, as defined by self report.

Exclusion criteria

Patients

  • Possess a co-existing neurological or psychiatric illness that, in the opinion of the study team, exclude the subject from participation
  • Demonstrate clinically significant dementia, as determined by the ALS study neurologist
  • Possess abnormal speech or swallowing processes due to a condition independent of their ALS diagnosis

Listeners

  • Have an identified speech, language, learning, or neurological disorders per self-report
  • Experience communicating with people with motor speech disorders

Treatment and study plan

Digital recording of speech and swallow sounds using the Beiwe Digital Health App on a personal smartphone

Device

[Patients only] Weekly completion of audio recordings of speech and swallowing performed at home by the subject using the study smartphone application on their personal device.

Modified Barium Swallow Study (MBSS)

Radiation

[Patients only] MBSS is an instrumented evaluation of oropharyngeal swallowing function that is performed using videofluoroscopy.

Other names: Videofluoroscopic Swallowing Study (VFSS)

Speech Intelligibility Test (SIT)

Behavioral

[Patients only] The SIT is a standardized test for measuring speech intelligibility.

SIT Scoring

Behavioral

[Listeners only] Listeners will judge the intelligibility of speech recordings made by patients in the study.

Primary outcomes

  1. Digital recording of speech and swallow

    Time frame: weekly for 24 weeks

    Audio recordings of speech tasks and spontaneous swallowing task

Secondary outcomes

  1. MBS Impairment Profile (MBSImp)

    Time frame: Weeks 0 and 24

    Standardized scoring for the MBSS in 17 domains. Domains are aggregated in to scores for Oral Impairment (0-22), Pharyngeal Impairment (0-29), and Esophageal Impairment (0-4), with higher scores indicating impaired function.

  2. Speech Intelligibility Task (SIT) Intelligibility listener scoring

    Time frame: Weeks 0, 12, and 24

    Listeners will score the intelligibility of patient SIT recordings

  3. ALS Functional Rating Scale - Revised (ALSFRS-R)

    Time frame: Weeks 0, 12, and 24

    ALS Specific Assessment of physical function ranging from 0-48, with 48 being normal function.

  4. Center for Neurological Study - Bulbar Function Scale (CNS-BFS)

    Time frame: Weeks 0, 4, 8, 12, 16, 20, and 24

    Self-administered rating scale for speech (7-49) and salivation (7-35) functions, with high scores indicating impaired function.

  5. Mann Assessment of Swallowing Ability (MASA)

    Time frame: Weeks 0, 12, and 24

    A standard clinical swallowing assessment performed by the speech-language pathologist. Scores range from 38-200, with lower scores indicating higher impairment.

  6. EAT-10 Questionnaire

    Time frame: Weeks 0, 12, and 24

    A self-reported assessment of eating and swallowing function. Scores range from 0-40, with higher scores indicating higher impairment.

  7. Forced Vital Capacity (FVC)

    Time frame: Weeks 0, 12, and 24

    A standard clinical respiratory assessment of vital capacity

  8. Maximal Inspiratory Pressure (MIP)

    Time frame: Weeks 0, 12, and 24

    A standard clinical respiratory assessment of inspiratory strength

Sponsors and collaborators

Lead sponsor

Milton S. Hershey Medical Center

Other

Collaborators

  • Congressionally Directed Medical Research Programs
  • Penn State University

Registry information

Official study title

Home Telemonitoring of Bulbar Function by Acoustic Measurement of Swallowing and Speech Sounds in ALS

Important dates

Study start
2022
Primary completion
2024
Study completion
2026
First posted
May 17, 2021
Registry last updated
Jun 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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