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Foundations for Prescribing Song-Based Therapies: A Quantitative Comparison of Laryngeal Exercises

Foundations for Prescribing Song-Based Therapies: A Quantitative Comparison of Laryngeal Exercises

Status
Withdrawn
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07595315
Acronym
SINGS
Enrollment
0
Registered
2026-05-19
Start date
2025-06-01
Completion date
2025-12-15
Last updated
2026-05-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dysphagia

Keywords

Song-based therapy, Music therapy, Surface EMG, EEG

Brief summary

SINGS explores the therapeutic potential of song-based exercises for treating dysphagia in geriatric populations. The project aims to compare the effectiveness of song-based tasks with traditional speech-language pathology (SLP) exercises using advanced tools such as surface electromyography (sEMG) and functional neuroimaging. In addition to quantifying functional activity during therapy, the study will assess patient compliance, satisfaction, and long-term swallowing outcomes, with a focus on improving quality of life through innovative, enjoyable therapies.

Interventions

OTHERDysphagia Treatment Protocol

The SINGS arm will be completed by all members in the cohort.

Sponsors

University of Kansas Medical Center
Lead SponsorOTHER
National Center for Advancing Translational Sciences (NCATS)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Participants are prospectively assigned to perform predefined speech-language pathology exercises and song-based tasks during a single study visit while EEG and surface EMG are recorded for mechanistic comparison. This is a basic science / physiologic study conducted in healthy adults with a cross-sectional, single-visit (\ 90 minutes) design.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Healthy Adults

Exclusion criteria

* History of head and neck cancer, radiation to the neck, and/or other head and neck based surgeries\* * Formal Dysphagia diagnosis\* * Formal GERD diagnosis\* * Adults unable to consent * Individuals who are not yet adults (infants, children, teenagers) * Prisoners

Design outcomes

Primary

MeasureTime frameDescription
Muscle ActivationDay 1 (single 90-minute study visit)Surface EMG readings between SBT and SLP tasks.
EEGDay 1 (single 90-minute study visit)Similar regional neural activity measured by EEG between SBT and SLP tasks.

Secondary

MeasureTime frameDescription
EAT-10 Total ScoreDay 1 (single study visit)Total score on the Eating Assessment Tool (EAT-10) questionnaire
Self-reported tobacco and e-cigarette useDay 1 (single study visit); assesses past 30 days and lifetime history as applicableSelf-reported tobacco and e-cigarette use variables (e.g., days used in past 30 days; cigarettes per day; quit attempts; age of initiation)
Patient Satisfaction SurveyDay 1 (single study visit)Likert-scale responses (1-5) on satisfaction, convenience, enjoyment, ease, and confidence comparing song-based tasks to SLP tasks

Contacts

PRINCIPAL_INVESTIGATORJennifer Villwock, MD

University of Kansas Medical Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 20, 2026