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Measuring Pharyngeal Muscle Improvements Following Behavioral Swallowing Exercises

Measuring Pharyngeal Muscle Improvements Following Behavioral Swallowing Exercises

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05080725
Enrollment
2
Registered
2021-10-18
Start date
2022-05-24
Completion date
2022-10-04
Last updated
2023-02-24

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

Conditions

Dysphagia

Brief summary

The purpose of this study is to learn more about how exercise and protein supply affect swallow muscles. Twenty healthy older adults will be recruited from local community centers, physician offices, and retirement communities via flyers. Participants will complete 16 sessions of standard of care swallowing exercises 2 times per week for 8 weeks. All sessions will be conducted via Zoom. During each session, a series of swallow exercises will be performed following a demonstration from a trained speech-language pathologist. Participants will be referred to NYU Langone Health or White Plains Hospital, for a videofluoroscopic swallowing study, acoustic pharyngometry and measures of hand grip strength before and after the treatment protocol. Patients will be able to select their preferred site for swallow study completion. Results will inform the relationship between swallow exercises and pharyngeal muscles. All devices and exercises are established as safe and effective and are FDA approved.

Detailed description

The natural next step in this program of research is to investigate interventions for reversing pharyngeal sarcopenia with the ultimate goal of developing novel therapeutic strategies to address this pervasive clinical issue. The exercise science literature suggests that sarcopenia in the limb muscles can be reversed through a combination of rigorous exercise and adequate levels of dietary protein. The innovative multi-disciplinary protocol, PEPP (Pharyngeal Exercises Plus Protein), combines pharyngeal swallowing exercises selected for their known activation of the pharyngeal muscles with daily supplemental protein drinks. The research lab had documented successful improvements to swallowing physiology and pharyngeal sarcopenia in a pilot series of 5 older women using PEPP. However the research was abruptly halted due to both ethical and feasibility challenges posed by the COVID-19 pandemic. In response to these challenges, this study is seeking to establish the feasibility and effectiveness when the PEPP intervention is delivered using telehealth (telePEPP).

Interventions

OTHERTelePEPP intervention

TelePEPP sessions will be conducted twice per week by a Speech Language Pathologist and/or graduate student clinician, on the study team. This clinician will deliver the intervention from the NYU Voice Center using the web conferencing software Webex (institutional license) on a Dell desktop computer with a 3.1 GHz intel core processor and high definition camera. Each exercise set will include 40 repetitions (10 reps of effortful swallows, tongue hold swallows, effortful pitch glides and maximal posterior tongue presses). All exercises are widely-adopted by clinicians as standard of care exercises. The number of sets will be gradually increased as tolerance builds \[2 sets in week 1, 3 sets in week 2, 4 sets in weeks 3+\].

Sponsors

NYU Langone Health
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to 120 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 65 and older * SARC-F score of ≥4 * Functional hearing and vision status * Access to reliable internet connection * Availability of caregiver/family support and/or comfort with independent technology usage

Exclusion criteria

* Known structural or neurological causes of dysphagia * Not suitable to consume high levels of protein supplementation (i.e. moderate to severe kidney dysfunction)

Design outcomes

Primary

MeasureTime frameDescription
Measurement of pharyngeal shortening after interventionSession 17 (9 week post-intervention visit)2D lateral videofluoroscopic images will be used to measure pharyngeal shortening pre and post intervention
Measurement of pharyngeal constriction before interventionSession 0 (Day 0 pre-intervention visit)2D lateral videofluoroscopic images will be used to measure pharyngeal constriction pre and post intervention
Measurement of pharyngeal constriction after interventionSession 17 (9 week post-intervention visit)2D lateral videofluoroscopic images will be used to measure pharyngeal constriction pre and post intervention
Measurement of pharyngeal shortening before interventionSession 0 (Day 0 pre-intervention visit)2D lateral videofluoroscopic images will be used to measure pharyngeal shortening pre and post intervention

Secondary

MeasureTime frameDescription
Measurement of pharyngeal wall thickness before interventionSession 0 (Day 0 pre-intervention visit)2D lateral videofluoroscopic images will be used to measure wall thickness pre and post intervention
Measurement of pharyngeal wall thickness after interventionSession 17 (9 week post-intervention visit)2D lateral videofluoroscopic images will be used to measure wall thickness pre and post intervention
Measurement of pharyngeal volume before interventionSession 0 (Day 0 pre-intervention visit)Acoustic Pharyngometry will be used to measure pharyngeal volume pre and post intervention.
Measurement of pharyngeal volume after interventionSession 17 (9 week post-intervention visit)Acoustic Pharyngometry will be used to measure pharyngeal volume pre and post intervention.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026