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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