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NCT05080725 · ClinicalTrials.gov registry record · NA
Measuring Pharyngeal Muscle Improvements Following Behavioral Swallowing Exercises
A NA study of Dysphagia, sponsored by NYU Langone Health.
- Completed
- Registry status
- NA
- Development phase
- 2
- Enrollment target
- 1
- Study location
NCT05080725 is a NA study of Dysphagia that has completed, run by NYU Langone Health. The registered enrollment target is 2 participants, below the 172-participant average among 35 other Dysphagia trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.
The verdict
NCT05080725, a NA study of Dysphagia, has completed, sponsored by NYU Langone Health.
- COMPLETED
- Registry status
- NA
- Development phase
- 2 participants
- Enrollment target
- 1
- Study location
Study 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.
Conditions Studied
Interventions
- OTHER TelePEPP intervention
Study Locations (1)
New York
- NYU Langone Health - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2 participants |
| Start Date | 2022-05-24 |
| Est. Completion | 2022-10-04 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05080725
The ClinicalTrials.gov registry entry for NCT05080725 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 2 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 172-participant average among 35 other Dysphagia trials with a reported enrollment target (99% lower). The listed sponsor is NYU Langone Health, which has 1,164 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Dysphagia appearing as the primary indexed condition, and to 1 intervention - of which TelePEPP intervention is the first listed.
NCT05080725 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.
Frequently Asked Questions
What is clinical trial NCT05080725 about?
NCT05080725 is a clinical study titled "Measuring Pharyngeal Muscle Improvements Following Behavioral Swallowing Exercises". 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 sw...
What is the current status of trial NCT05080725?
This trial is currently completed. It is a NA study. The enrollment target is 2 participants. The study started on 2022-05-24. Estimated completion is 2022-10-04.
What conditions does trial NCT05080725 study?
This clinical trial studies the following conditions: Dysphagia.
What interventions are being tested in trial NCT05080725?
The interventions under investigation include: TelePEPP intervention (OTHER).
Who is sponsoring clinical trial NCT05080725?
This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05080725 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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