Actively Recruiting
NLit and Outcomes in HNC Survivor-Caregiver Dyads
Led by University of Kansas Medical Center · Updated on 2025-06-15
150
Participants Needed
1
Research Sites
128 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this observational (cross-sectional) study is to better understand nutrition literacy in survivor-caregiver dyads and its impact on nutrition related outcomes and quality of life. We're interested in finding out how much they know about nutrition and how this might relate to their overall health, body composition, functional status, and overall well-being. We will target post-treatment head and neck cancer survivors and a paired informal caregiver. The main questions we aim to answer are: * How does the nutrition literacy of both the survivor and caregiver relate to their sociodemographic, behavioral, and clinical characteristics? * How dyadic nutrition literacy influence individual nutrition outcomes like skin carotenoid levels, body composition, and functional status? * Does the shared nutrition knowledge (nutrition literacy) of both the survivor and caregiver impact their quality of life together? Participants will: Answer questions about their knowledge of nutrition. Have their nutritional health status checked. Use a non-invasive device to measure skin carotenoid content to validate self-reports of fruit and vegetable intake. Have a simple and painless test to measure their body composition - like how much muscle and fat they have. Do some physical tests like grip strength and walking to measure their physical ability. Answer questions about their general well-being and lifestyle, like exercise and diet. (For the survivor) Share details about their cancer, its treatment, and their overall well-being. (For the caregiver) Answer questions about their role in taking care of the survivor, and their involvement in care routine such as food shopping and cooking.
CONDITIONS
Official Title
NLit and Outcomes in HNC Survivor-Caregiver Dyads
Who Can Participate
Eligibility Criteria
You may qualify if you...
- History of oral cavity, pharyngeal, or laryngeal cancer in survivor
- Survivor is between 6 months and 4 years post-primary oncology treatment
- Survivor has no evidence of disease
- Survivor has an informal caregiver who shares or primarily handles food shopping and/or preparation
- Survivor does not use a feeding tube as primary nutrition source and can eat orally
- Participants are 18 years or older
- Participants are English-speaking
You will not qualify if you...
- Dementia or organic brain syndrome in survivor or caregiver
- Severe emotional distress in survivor or caregiver
- Active schizophrenia in survivor or caregiver
- Diagnosis of another cancer in past five years (excluding skin or cervical cancer in situ) in survivor or caregiver
- Adults unable to consent
- Individuals under 18 years old
- Pregnant women
- Prisoners
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University of Kansas Medical Center
Kansas City, Kansas, United States, 66160
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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