AI-Based Speech Intelligibility Assessment: Efficacy & Reliability

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorPusan National University Yangsan Hospital

About this trial

compare the auditory-perceptual assessment conducted by speech-language pathologists using the U-TAP with the assessment performed via the AI solution (Blings) program in patients with speech disorders, and to evaluate the efficacy and reliability of these two methods for speech intelligibility assessment.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adults aged 18 years or older.

Patients with neurologic disorders, including amyotrophic lateral sclerosis, poliomyelitis, cerebellar disorders, cerebellar lesions, and stroke.

Patients presenting with concomitant speech disorders, such as dysarthria, motor speech disorders, and voice disorders.

Disqualifiers

Subjects with a score of less than 16 points on the Korean Mini-Mental State Examination (K-MMSE).

Subjects with visual, perceptual, or auditory impairments that prevent them from following the examiner's instructions.

Subjects judged by the researcher as unsuitable for participation in this clinical study due to other reasons.

Trial population

The study population consists of adult patients aged 18 years or older with neurologic disorders-including amyotrophic lateral sclerosis (ALS), poliomyelitis, cerebellar-related disorders (such as cerebellar atrophy or degeneration and cerebellar lesions), and stroke-who present with concomitant speech disorders, such as dysarthria, motor speech disorders, and voice disorders. Participants must have sufficient cognitive function, defined as a Korean Mini-Mental State Examination (K-MMSE) score of 16 or higher, and must be capable of understanding and following the examiner's instructions. Individuals with visual, perceptual, or auditory impairments that interfere with participation in speech assessment, as well as those deemed unsuitable for study participation by the investigator for other clinical or practical reasons, are excluded.

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

40 Participants
are grouped into 1 trial group
Group A: Observational study(Patients with speech disorders)

Trial outcomes

Primary outcomes

1

Word-level consonant accuracy (%) derived from speech samples obtained during the U-TAP assessment

The agreement between consonant accuracy analyzed by the AI-based speech disorder analysis program (Blings) and the evaluations conducted independently by two certified speech-language pathologists (Rater 1 and Rater 2). Consonant accuracy is calculated at the word level and expressed as a percentage score ranging from 0% to 100%. The mean value of consonant accuracy scores from Rater 1 and Rater 2 is used as the reference human evaluation.

Time frame
Visit 1 (Baseline)

Secondary outcomes

1

Test-retest reliability of word-level consonant accuracy (%) calculated by Blings

The consistency of consonant accuracy scores generated by Blings from the same participant across two visits. Comparison of Blings-derived consonant accuracy scores (%) between Visit 1 and Visit 2. Scores range from 0% to 100%.

Time frame
Visit 1 and Visit 2 (7 ± 5 days interval)
2

Inter-rater agreement of word-level consonant accuracy (%) among Blings, Rater 1, and Rater 2

Agreement in consonant accuracy evaluations between the AI-based analysis and human raters. Pairwise comparisons: Rater 1 vs. Rater 2, Blings vs. Rater 1, Blings vs. Rater 2. Scores expressed as percentages (0-100%)

Time frame
Visit 1 and Visit 2 (7 ± 5 days interval)
3

Time required to complete speech analysis (seconds)

Comparison of analysis time between the AI-based system (Blings) and human raters. Total analysis time measured in seconds for: Rater 1, Rater 2, Blings

Time frame
Visit 1 and Visit 2 (7 ± 5 days interval)

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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