NCT06609057

Brief Summary

This clinical trial evaluates a nutritional intervention called Cooking for Your Health in Southern New Mexico for improving diet quality and knowledge related to nutrition and cancer prevention among individuals living in the Southern region of New Mexico. New Mexico border communities have high rates of cancer and obesity, both exacerbated by poor diet quality. Traditional Mexican diets are high in fruit, vegetables, and fiber, but are intensive to prepare and not practical for many families living in New Mexico now. Vegetable oils, such as canola, safflower, and sunflower oils, are commonly used in cooking within the regional New Mexican community because they are inexpensive and readily available; however, they may not be as healthy as other options. Interventions focused on teaching proper cooking techniques and raising awareness about nutritious foods have shown positive behavior changes, including greater preference for healthier foods, increased confidence in food preparation and cooking a balanced meal, and higher vegetable variety and availability in the home. This study may help identify effective and culturally relevant real-world strategies to improve knowledge, skills, behaviors, and access to resources to improve nutrient intake, with the long-term goal of decreasing cancer risk and chronic disease risk in southern New Mexican communities.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
1mo left

Started Oct 2024

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress96%
Oct 2024Aug 2026

First Submitted

Initial submission to the registry

September 20, 2024

Completed
3 days until next milestone

First Posted

Study publicly available on registry

September 23, 2024

Completed
19 days until next milestone

Study Start

First participant enrolled

October 12, 2024

Completed
1.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 30, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 30, 2026

Last Updated

January 22, 2026

Status Verified

January 1, 2026

Enrollment Period

1.9 years

First QC Date

September 20, 2024

Last Update Submit

January 21, 2026

Conditions

Outcome Measures

Primary Outcomes (4)

  • Accrual rate

    The intervention will be considered feasible if accrual goals are met within 6 months of trial activation. Will be summarized using descriptive statistics. Results will be assessed separately for Part I and Part II, as well as for both groups combined.

    Within 6 months of trial activation

  • Engagement

    The intervention will be considered feasible if \>= 70% of participants attend \>= 70% of sessions. Will be summarized using descriptive statistics. Results will be assessed separately for Part I and Part II, as well as for both groups combined.

    Up to 8 weeks

  • Retention

    The intervention will be considered feasible if \>= 70% of participants complete the week 8 food frequency questionnaire. Will be summarized using descriptive statistics. Results will be assessed separately for Part I and Part II, as well as for both groups combined.

    At week 8

  • Acceptability

    The intervention will be considered feasible if \>= 70% or more of participants state that the program and study processes were acceptable, appropriate, and feasible. Acceptability will assess: intervention pre-work and in-class work activities, as well as specific data collection methods. Will be summarized using descriptive statistics. Results will be assessed separately for Part I and Part II, as well as for both groups combined.

    Up to 8 weeks

Study Arms (1)

Prevention (nutrition intervention)

EXPERIMENTAL

Participants attend Cooking for Your Health in Southern New Mexico intervention sessions, consisting of 15-30 minutes of pre-work (watching an educational video and/or practicing a new culinary skill), 60 minutes of hands-on experiential cooking and culinary session in a teaching kitchen, and a 60 minute meal that includes group discussion of educational information, QW for 6 weeks.

Other: Nutritional InterventionOther: Questionnaire AdministrationOther: Survey AdministrationOther: Discussion

Interventions

Receive Cooking for Your Health in Southern New Mexico intervention

Prevention (nutrition intervention)

Ancillary studies

Prevention (nutrition intervention)

Ancillary studies

Prevention (nutrition intervention)

Ancillary studies

Also known as: Discuss
Prevention (nutrition intervention)

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • + years of age
  • Part I: Fluent in English (Otero and Doña Ana Counties); Part II: Fluent in English (Otero County) and fluent in Spanish (Doña Ana County)
  • Able to understand and willing to sign a written informed consent in either English or in Spanish (Part II only: Doña Ana County only)
  • Access to phone for study contacts
  • Be willing and able to attend the 6 in-person classes
  • Access to internet to complete study assessments and access study website
  • Willingness to participate in all study activities
  • Completion of all baseline data collection activities
  • No prior clinical diagnosis of diabetes

You may not qualify if:

  • Under 18 years of age, or over 70 years of age
  • Not fluent in either Spanish or English (Part II only: Doña Ana County only)
  • Unable to understand or unwilling to sign written informed consents in English or in Spanish (Part II only: Doña Ana County only)
  • No access to phone
  • Unwilling or unable to attend the 6 in person classes
  • No access to internet
  • Unwilling to participate in all study activities
  • Unable to complete all run in activities
  • Prior clinical diagnosis of diabetes

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

New Mexico State University

Las Cruces, New Mexico, 88003, United States

RECRUITING

Study Officials

  • Heather Greenlee, ND, PhD

    Fred Hutch/University of Washington Cancer Consortium

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Jenny Whitten-Brannon

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 20, 2024

First Posted

September 23, 2024

Study Start

October 12, 2024

Primary Completion (Estimated)

August 30, 2026

Study Completion (Estimated)

August 30, 2026

Last Updated

January 22, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Locations