NCT06030011Recruiting
Implementing the NYU Electronic Patient Visit Assessment (ePVA) for Head and Neck Cancer In Rural and Urban Populations
Source: ClinicalTrials.gov · Last updated 6 Jul 2026
Brief summary (registry, in English)
The PI and the research team developed the New York University (NYU) Electronic Patient Visit Assessment (ePVA) for head and neck cancer (HNC) as a patient-reported outcome measure (PRO) for the early detection of uncontrolled symptoms. The ePVA is digital patient-reported symptom monitoring system, providing actionable information at point-of-care that enables clinicians to provide real-time interventions. The study aims to advance the science of cancer care delivery by testing the effectiveness of the ePVA as a digital patient-reported monitoring system for patients with HNC in real-world settings and identify implementation strategies that optimize the effectiveness of the ePVA in diverse rural and urban settings. The study hypothesis is that participants assigned to the ePVA arm will have better swallowing, taste and smell, and social function than participants assigned to usual care arm at 4 weeks after completing radiation therapy.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 270 (estimated)
- First submitted
- 1 Sept 2023
- Start date
- 25 Jun 2024
- Primary completion date
- 31 Aug 2028
- Lead sponsor
- The University of Texas Health Science Center, Houston
- Diseases
- Head and neck cancer
- NCT number
- NCT06030011
What you commit to
- Study type: Interventional
- Planned participants: 270
- From 25 Jun 2024 to the primary completion date, 31 Aug 2028
- 5 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Any medical condition that could limit the participant's ability to provide informed consent and complete the questionnaires.
Who the study is looking for
- Individuals with histologically diagnosed head and neck cancer (HNC) undergoing curative radiation therapy with or without chemotherapy
- English or Spanish speaking
- Clinicians (i.e., physicians, nurses, dentists, physician assistants, social workers, nutritionists, speech swallow therapists) caring for patients with head and neck cancer at the participating institutions
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (5)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| UTHealth Houston Cizik School of Nursing Coordinator of this site? Confirm its status | Houston | United States | Not yet recruiting |
| University of Kansas Cancer Center Coordinator of this site? Confirm its status | Kansas City | United States | Recruiting |
| NYU Meyers College of Nursing Coordinator of this site? Confirm its status | New York | United States | Not yet recruiting |
| NYU Langone Perlmutter Cancer Center Coordinator of this site? Confirm its status | New York | United States | Recruiting |
| Fox Chase Cancer Center Coordinator of this site? Confirm its status | Philadelphia | United States | Not yet recruiting |
Related publications
This page is information, not medical advice. Discuss any trial with your doctor.