Nutrition literacy in head and neck cancer survivors and their caregivers
Official title: Nutrition Literacy and Associated Outcomes in Head and Neck Cancer Survivor-caregiver Dyads
Run by University of Kansas Medical Center · NCT07021885 · Data updated 2026-11-12
We will see if nutrition knowledge in head and neck cancer survivors and their informal caregivers relates to body composition, nutrition biomarkers, physical function, and quality of life.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 150 (estimated) |
| Sponsor | University of Kansas Medical Center Academic / other |
| Locations | 1 site (Kansas City, Kansas) |
| Status | Recruiting |
| Started | December 1, 2023 |
| Main results expected | August 16, 2025 |
| Study ends | May 16, 2026 |
| Registry record updated | June 15, 2025 |
| Trial ID | NCT07021885 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (age 18+) who are 6 months to 4 years post-primary treatment for oral cavity, pharyngeal, or laryngeal cancer, have no evidence of disease, can eat orally (no primary feeding tube), speak English, and have an informal caregiver involved in food procurement or preparation are ideal candidates.
✕Probably not a fit
People with active or recent other cancers, severe mental illness or cognitive impairment, primary feeding-tube dependence, non–English speakers, minors, pregnant women, or prisoners are excluded and unlikely to benefit from participation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This cross-sectional observational project enrolls post-treatment head and neck cancer survivors (6 months–4 years after primary treatment) paired with an informal caregiver who helps with food shopping or preparation. Participants complete questionnaires measuring nutrition literacy and sociodemographic and behavioral characteristics, and undergo measurements including skin carotenoid levels, body composition, and functional status alongside quality-of-life surveys. Data from survivor-caregiver dyads will be analyzed to explore how individual and shared nutrition knowledge correlates with objective nutrition markers and patient-reported outcomes. Results aim to identify patterns that could guide tailored nutrition education or supportive services for survivors and their caregivers.
Why it matters
Potential benefit: If successful, the findings could help tailor nutrition education and support for survivors and caregivers to improve diet-related health, physical function, and quality of life.
How similar studies have gone: Previous research has linked nutrition literacy to dietary behaviors and outcomes in cancer populations, but dyadic studies focused on head and neck cancer survivors and caregivers are limited, making this approach relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Survivors and their caregivers will be eligible to participate if the survivor 1) has a history of oral cavity, pharyngeal, or laryngeal cancer, 2) is between 6 months - 4 years post-primary oncology treatment, 3) has no evidence of disease, 4) has an informal caregiver living in or out of the home who has a shared or primary role in food procurement and/or preparation, 5) no current use of feeding tube as the primary source of nutrition and can consume food orally, 6) age 18+, 7) English-speaking. Survivors and their caregivers will not be eligible to participate if either has 1) dementia or organic brain syndrome; 2) severe emotional distress; 3) active schizophrenia, 4) another diagnosis of cancer in the past five years (not including skin or cervical cancer in situ). Exclusion Criteria: * Adults unable to consent * Individuals who are not yet adults (infants, children, teenagers) * Pregnant women * Prisoners
Where it's running
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University of Kansas Medical Center
Kansas City, Kansas, United States Recruiting
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.