Viewing Study NCT06643455



Ignite Creation Date: 2024-10-26 @ 3:42 PM
Last Modification Date: 2024-10-26 @ 3:42 PM
Study NCT ID: NCT06643455
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-09-27

Brief Title: Mindfulness Intervention for Improving Nutrition in the Digital Kitchen Among Stage I-III Breast Cancer Survivors MIND Trial
Sponsor: None
Organization: None

Study Overview

Official Title: Mindfulness Intervention for Nutrition in the Digital Kitchen MIND Study A Pilot and Feasibility Study
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This trial tests how well a remotely-delivered nutrition and culinary intervention works to improve diet quality among stage I-III breast cancer survivors Despite the strong evidence demonstrating the benefits of healthy nutrition on improving cancer outcomes most breast cancer survivors do not meet the nutrition recommendations The use of technology in behavioral interventions is proving to be a cost-effective mode of delivering lifestyle education to promote behavior change The Mindfulness Intervention for Nutrition in the Digital Kitchen MIND program is delivered through a learning management system on the Cook for Your Life platform cookforyourlifeorg The Cook for Your Life platform is a cancer patient-facing interactive program offering free nutrition and healthy cooking information recipes and cooking videos that disseminate evidence-based information on nutrition and cancer survivorship The MIND program may help improve diet quality and increase fruit and vegetable intake among stage I-III breast cancer survivors
Detailed Description: OUTLINE Patients are randomized to 1 of 2 arms

ARM A INTERVENTION Patients participate in the MIND program consisting of self-paced online education on nutrition chef demo skills-building cooking and mindfulness practice over 4 hours weekly for 6 weeks

ARM B WAITLIST CONTROL Patients participate in standard of care SOC for 6 weeks Patients may optionally receive access to the MIND program following the initial 6-week study period

After completion of study intervention patients are followed up at 12 weeks

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None