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Digital Assessment of Speech and Fine Motor Control in ALS

Recruiting
Conditions
Progressive Muscular Atrophy
Primary Lateral Sclerosis
Amyotrophic Lateral Sclerosis
Interventions
Behavioral: Digital Speech and Handwriting Assessment
Registration Number
NCT06315673
Lead Sponsor
Milton S. Hershey Medical Center
Brief Summary

This is a single-session, case-control study that incorporates digital tools for assessing speech and motor function in motor neuron disease. Patients with motor neuron disease (including amyotrophic lateral sclerosis (ALS), primary lateral sclerosis (PLS), and progressive muscular atrophy (PMA)) and age-matched healthy controls will be enrolled. Subjects will complete a speech and handwriting assessment during the study visit on a tablet computer (BioSensics LLC, Newton, MA). We will explore whether these digital biomarkers are sensitive to functional disease severity as reported by the ALS Functional Rating Scale - Revised (ALFRS-R) \[1\]. We will also compare assessment data between the patient and control groups.

Detailed Description

ALS is a progressive neuromuscular disease that causes weakness and inevitably affecting multiple motor processes within the body. To assess changes in functional mobility, clinicians and clinical investigators often rely on the ALS Functional Rating Scale - Revised (ALSFRS-R), a standardized 12-item questionnaire that has been in use for decades. Although thoroughly validated, this scale has received criticism for providing a coarse reflection of a patient's disease, scaling non-linearly within and across functional domains, and without the sensitivity to reflect day-to-day variability or small but meaningful changes.

This study includes collection of digital speech and fine motor control assessment data at a single study visit. Features extracted from this data will be compared with standard clinical disease outcome measures and also the features derived from control participant data. We will use these comparisons to explore the use of these digital assessments in capturing the range of functional changes that occur in ALS and the related motor neuron diseases of PLS and PMA that are regularly treated in the ALS clinic.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
50
Inclusion Criteria
  1. [Patient Group Only] Diagnosis of definite, probable, probable laboratory-supported, or possible ALS by revised El Escorial research criteria [Brooks2000], primary lateral sclerosis (PLS), or progressive muscular atrophy (PMA).

  2. [Patient Group Only] at least minimal speech or handwriting ability

    1. ALSFRS-R speech score of 2 ("intelligible speech with repeating") or greater, OR
    2. ALSFRS-R handwriting score of 2 ("not all words are legible") or greater.
  3. [Control Group Only] Possess no neurological or orthopedic problems that affects their speech or handwriting AND age-matched to the existing patient cohort.

  4. 18 years of age or older;

  5. Fluent in written and spoken English.

Exclusion Criteria
  1. Currently or previously enrolled in STUDY00013892 (NCT05271435)
  2. Neurological or orthopedic problems (independent of their inclusionary diagnosis for the patient group) that affects their speech or handwriting
  3. Pregnant or nursing woman
  4. Prisoner or institutionalized individuals
  5. Have any clinically relevant medical history of other disease or diseases that, in the opinion of the research team, exclude the subject from participation (including severe cognitive dysfunction).

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
ControlDigital Speech and Handwriting AssessmentIndividuals with no neurological or orthopedic problems that affects their speech or handwriting AND age-matched to the existing patient cohort.
PatientDigital Speech and Handwriting AssessmentIndividuals with diagnosis of definite, probable, probable laboratory-supported, or possible ALS by revised El Escorial research criteria \[2\], primary lateral sclerosis (PLS), or progressive muscular atrophy (PMA).
Primary Outcome Measures
NameTimeMethod
Speaking rate during a standardized passagebaseline

Speaking rate, in words per minute, will be determined from an audio recording of a standardized reading passage.

Residual on spiral tracing taskbaseline

Handwriting tasks include tracing of a spiral. The average residual, or deviation from the target spiral (in pixels), will be determined from the handwriting file associated with the tracing task.

Secondary Outcome Measures
NameTimeMethod
ALS Functional Rating Scale- Revised (ALSFRS-R)baseline

The ALSFRS-R measures 12 aspects of physical function, ranging from one's ability to swallow and use utensils to climbing stairs and breathing. Each function is scored from 4 (normal) to 0 (no ability), with a maximum total score of 48 and a minimum total score of 0.

Strength testingbaseline

Strength testing is performed by the attending neurologist at clinical appointments. Bilateral deltoids, biceps, triceps, wrist extension, and interossei strength will be documented according to Medical Research Council (MRC) grade 0 (no power) to 5 (normal power). Total score for bilateral muscle groups ranges from 0 to 50.

Forced vital capacity (FVC)baseline

FVC is collected at clinical appointments by a respiratory therapist. FVC is the volume of air that is forcefully expelled into a spirometer. FVC is expressed as a percentage (%) of predicted volume against an age, height, and ethnicity matched standard. The best result of three trials is used.

Upper motor neuron functionbaseline

Reflex testing is performed by the attending neurologist at clinical appointments. Bilateral biceps, triceps, and brachioradialis reflexes will be documented according to Modified Ashworth Scale grade 0 (no tone increase) to 4 (limb rigid). Total score for bilateral muscle groups ranges from 0 to 24.

Trial Locations

Locations (1)

Milton S. Hershey Medical Center

🇺🇸

Hershey, Pennsylvania, United States

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