High Resolution Pharyngeal Manometry (HRPM) Biofeedback

Starting soon · Not applicable

Conditions studied: Healthy

In brief

The purpose of this study is to quantify the added benefit of visual biofeedback from High Resolution Pharyngeal Manometry (HRPM) for swallowing rehabilitation. Primary aims including assessing changes in swallowing biomechanics (pressure generation, timing) during swallow maneuvers with and without HRPM visual biofeedback. Secondary aim includes participant attitudes related to visual biofeedback and the experience of HRPM.

Key facts

Study ID

NCT07508059

Run by

NYU Langone Health

People needed

50

Starts

2026-05-01

Expected to finish

2027-05-01

Last updated by the study team

2026-04-02

Who can join

Age: 18 and older, up to 40. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Participants must be independent community dwelling adults.
• Participants must be between the ages of 18-40 years old.
• Willingness to consent and participate in the study procedures.
• No reported dysphagia or difficulty swallowing evidenced by an EAT-10 Score <3.

You may not qualify if…

• Known structural or neurological causes of dysphagia (e.g., stroke, brain injury, or head/neck cancer).
• Recent or remote history of swallowing therapy; familiarity with swallowing maneuvers from relevant coursework as applicable (i.e., speech language pathology students).

Where it is running

• NYU Langone Health — New York, New York, United States

Full record on ClinicalTrials.gov

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