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Enhancing Quality of Life in Cancer Patients Through Tailored Nutrition Support: a Comprehensive Approach

Not Applicable
Recruiting
Conditions
Cancer
Interventions
Other: Nutritional support tool
Registration Number
NCT06628141
Lead Sponsor
UOMi Cancer Center
Brief Summary

The study aims to investigate the impact of a dedicated nutritional assistance tool on patients with cancer and to measure its effects on several proposed indicators.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
120
Inclusion Criteria
  • Patients affected by cancer, who decided to participate to the study, signed the informed consent and whose life expectancy is higher than 1 (one) year.
Exclusion Criteria
  • Patients with an eating disorder of psychiatric or psychological origin, diagnosed before cancer treatment.
  • Any other exclusion criteria as determined by the oncologist based on the patient's ability to successfully complete the program.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Nutritional support toolNutritional support tool-
Primary Outcome Measures
NameTimeMethod
Outcome Measure: Dietary Adherence1 year

Dietary adherence will be measured by comparing the planned recipes provided to participants with the meals they report consuming each week. Participants receive 21 recipe suggestions (7 breakfasts, 7 lunches, 7 dinners) via a mobile app. The following tools and methods will assess adherence:

Mobile Application Tracking: The app tracks participants' views of recipes and ingredient purchases via the integrated shopping list.

Weekly Questionnaire: A self-reported questionnaire asks if participants:

Followed the recipes using ingredients purchased via the app. Prepared recipes with their own ingredients. Ate meals not included in the plan. Adherence Calculation: Adherence is calculated as the ratio of recipes followed (via app or self-preparation) to the total number of recommended recipes (21 per week), expressed as a percentage.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

UOMI Cancer Center Clínica Mi Tres Torres

🇪🇸

Barcelona, Spain

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