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Trial Title: Development and Testing of Nutritional Algorithms (NACHO)

NCT ID: NCT05825469

Condition: Nutrition Poor
Nutritional Deficiency
Quality of Life

Conditions: Official terms:
Malnutrition

Conditions: Keywords:
Poor Nutrition
Nutritional Deficiency
Quality of Life

Study type: Interventional

Study phase: N/A

Overall status: Not yet recruiting

Study design:

Allocation: N/A

Intervention model: Single Group Assignment

Primary purpose: Supportive Care

Masking: None (Open Label)

Intervention:

Intervention type: Behavioral
Intervention name: Nutrition Algorithm
Description: A technology-based platform for a person-centered nutrition program, providing suggested foods and recipes from dietitians.
Arm group label: Nutrition Algorithm (NACHO)

Other name: Nutrition Algorithm for Cancer Health Outcomes (NACHO) Program

Summary: The goal of this research study is to develop a nutrition algorithm to optimize nutritional status and improve quality of life during for participants who are completing or have completed cancer treatment. The name of the intervention used in this research study is: Nutrition Algorithm for Cancer Health Outcomes (NACHO) (a technology-based platform that houses the algorithms for the person-centered nutrition program)

Detailed description: This is a longitudinal, mixed-methods, pilot descriptive study to develop a nutrition algorithm for cancer patients based on the Cancer Nutrition Consortium (CNC) study findings and refined through a dietitian panel participants and from feedback from participants and Family Advisory Council (PFAC) members. Research study procedures include screening for eligibility, interviews and/or focus groups, dietitian panel meetings, and surveys. Participation in this study is expected to last about 12 months. It is expected about 130 people will participate in this research study.

Criteria for eligibility:
Criteria:
Inclusion Criteria for Dietitians/Oncology clinicians - Have worked with at least 3 patients at the study site who had nutritional challenges Inclusion Criteria for Patient and Family Advisory Council (PFAC) participants - Current member of adult PFAC - > 18 years old Inclusion Criteria for Patient participants - > 18 years old - Able to speak and read English - Completed primary treatment (aim 2b) or actively undergoing treatment (aim 2b and aim 3, exploratory) - Access to a device (e.g., computer, tablet, smartphone) through which they can receive and engage with a REDCap link Exclusion Criteria for Patient Participants • Provider does not recommend

Gender: All

Minimum age: 18 Years

Maximum age: N/A

Healthy volunteers: No

Locations:

Facility:
Name: Dana Farber Cancer Institute

Address:
City: Boston
Zip: 02115
Country: United States

Start date: December 1, 2024

Completion date: December 31, 2025

Lead sponsor:
Agency: Dana-Farber Cancer Institute
Agency class: Other

Collaborator:
Agency: Cancer Nutrition Consortium Inc.
Agency class: Other

Source: Dana-Farber Cancer Institute

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05825469

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