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NCT06520579 · ClinicalTrials.gov registry record · NA
Anterior Cervical Discectomy and Fusion (ACDF) - Behavioral Intervention
A NA study of Dysphagia, sponsored by NYU Langone Health.
- Recruiting
- Registry status
- NA
- Development phase
- 50
- Enrollment target
- 1
- Study location
NCT06520579 is a NA study of Dysphagia that is actively recruiting participants, run by NYU Langone Health. The registered enrollment target is 50 participants, below the 171-participant average among 35 other Dysphagia trials with a reported enrollment target (71% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06520579, a NA study of Dysphagia, is actively recruiting participants, sponsored by NYU Langone Health.
- RECRUITING
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
This study will prospectively recruit and enroll patients undergoing primary Anterior Cervical Discectomy and Fusion (ACDF) surgeries at NYU Langone. Participants will undergo pre-operative and six-week post-operative swallowing assessment using videofluoroscopy (VFSS). Acoustic voice samples and Patient Reported Outcome Measures (PROMs) for swallowing and voice will also be collected. Beginning one-week before surgery participants will begin a behavioral health program that will be continued for six-weeks after surgery. The primary goal of this study will be to determine whether a preventative behavioral health program improves instrumental measures of swallowing and voice six-weeks after ACDF surgery. .
Conditions Studied
Interventions
- BEHAVIORAL Proactive pharyngeal-laryngeal Exercise Program
- DIETARY_SUPPLEMENT Premier Protein Clear ® High Protein
- BEHAVIORAL Hydration Counseling
Study Locations (1)
New York
- NYU Langone Health - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2024-10-15 |
| Est. Completion | 2026-09-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06520579
The ClinicalTrials.gov registry entry for NCT06520579 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 171-participant average among 35 other Dysphagia trials with a reported enrollment target (71% 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 3 interventions - of which Proactive pharyngeal-laryngeal Exercise Program is the first listed.
NCT06520579 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.
Frequently Asked Questions
What is clinical trial NCT06520579 about?
NCT06520579 is a clinical study titled "Anterior Cervical Discectomy and Fusion (ACDF) - Behavioral Intervention". This study will prospectively recruit and enroll patients undergoing primary Anterior Cervical Discectomy and Fusion (ACDF) surgeries at NYU Langone. Participants will undergo pre-operative and six-week post-operative swallowing assessment using videofluoroscopy (VFSS). Acoustic voice samples and Pa...
What is the current status of trial NCT06520579?
This trial is currently recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2024-10-15. Estimated completion is 2026-09-01.
What conditions does trial NCT06520579 study?
This clinical trial studies the following conditions: Dysphagia.
What interventions are being tested in trial NCT06520579?
The interventions under investigation include: Proactive pharyngeal-laryngeal Exercise Program (BEHAVIORAL), Premier Protein Clear ® High Protein (DIETARY_SUPPLEMENT), Hydration Counseling (BEHAVIORAL).
Who is sponsoring clinical trial NCT06520579?
This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06520579 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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