See if visual biofeedback helps swallowing maneuvers in healthy adults

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study compares swallowing maneuvers performed with and without high-resolution pharyngeal manometry (HRPM) visual biofeedback. The goal is to quantify changes in swallowing biomechanics such as pressure generation and timing. Secondary outcomes include participant attitudes toward biofeedback and the HRPM experience. The study involves adults aged 18-40 without swallowing difficulties and is conducted at NYU Langone Health. Participation requires consent and willingness to undergo HRPM-based procedures.

Why it matters

Who can join: the full rules

Inclusion Criteria:

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

Exclusion Criteria:

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

Where it's running

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

Study contacts

• Principal investigator: Sonja Molfenter — NYU Langone Health
• Study coordinator: Sonja Molfenter
• Email: Smm16@nyu.edu
• Phone: 212-992-7694

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.