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Developing an Ecological and Tailored Nutritional Intervention to Improve Quality of Life

This study aims to apply and assess the clinical feasibility of a health behavior theory-based ecological nutrition intervention program, providing nutrition care tailored to the unmet needs of esophageal cancer survivors after surgery. Esophageal cancer survivors will receive a 4-week nutrition intervention program ta

Condition(s)Esophageal Cancer
StatusRecruiting
PhaseNA
Study typeInterventional
SummaryThis study aims to apply and assess the clinical feasibility of a health behavior theory-based ecological nutrition intervention program, providing nutrition care tailored to the unmet needs of esophageal cancer survivors after surgery. Esophageal cancer survivors will receive a 4-week nutrition intervention program tailored to their individual nutritional needs. The program includes providing nutritional guidelines, customized care food, encouraging walking through a wearable device, and weekly telephone counseling. The evaluation of the program will assess food intake, adherence to dietary guidelines, activity level, nutritional indicators (such as PNI and NRI), weight change, fatigue, symptoms, quality of life, and satisfaction with meals and services. Additionally, interviews will be c
Who can participateInclusion Criteria: * Patients with clinical stage 1-3 primary esophageal cancer at diagnosis who have planned or received treatment, including esophageal resection and reconstruction, with curative intent, and their families\*. * You are at least 18 years of age * Have a native-level understanding of Korean * Who consented to this study Exclusion Criteria: * Concurrent multiple cancers at the time of diagnosis or a history of diagnosed and treated other organ cancers within the past year at the time of diagnosis * Have had esophageal resection and reconstruction surgery for other reasons before being diagnosed with esophageal cancer * Persons with limited cognitive and communication abilities * The patient has had problems progressing to oral feeding after surgery, requiring a concurrent
Ages18 Years
SexAll
Lead sponsorSamsung Medical Center
LocationsSeoul, Seoul, South Korea
Start date2025-04-03
NCT IDNCT07024849
Official listinghttps://clinicaltrials.gov/study/NCT07024849

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