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Cooking for Health Optimization With Patients (CHOP)

Tulane University logo

Tulane University

Status and phase

Completed
Phase 2
Phase 1

Conditions

Hypertension
Nutrition Disorders
Physical Activity
Diabetes
Obesity
Cardiovascular Diseases
Depression
Cancer
Cardiovascular Risk Factor

Treatments

Behavioral: Treatment

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Cooking for Health Optimization with Patients (CHOP) is the first known multi-site prospective cohort study with a nested Bayesian adaptive randomized trial in the preventive cardiology field of culinary medicine. It is also the first known longitudinal study to assess the impact of hands-on cooking and nutrition education on patient outcomes, with those classes taught by medical students and other future and current medical professionals who have first been trained in those classes on how to integrate diet and lifestyle counseling of patients with their respective scopes of clinical practice. CHOP is the primary research study of the world's first known medical school based teaching kitchen, The Goldring Center for Culinary Medicine at Tulane University School of Medicine. Medical trainees and professionals are followed in this study long-term to understand how the classes impact their competencies in patient counseling, attitudes about the counseling, and their own diets. Patients who consent to being randomized to these classes compared to standard of care are studied within the nested Bayesian adaptive randomized trial to understand how the classes impact their health outcomes, clinical and food costs, and the costs of health systems caring for these patient populations. CHOP is designed as a pragmatic population health trial to hopefully improve healthcare effectiveness, equity, and cost by establishing an evidence-based, scalable, sustainable model of healthcare intervention targeting the social determinants of health, while complementing the pharmacological and/or surgical management of patients.

Enrollment

7,192 patients

Sex

All

Ages

7 to 115 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 7 to 115 years of age (patients), and currently a medical trainee or professional (including for physicians, nurses, physician assistants, and dieticians)

Exclusion criteria

  • Inability to complete at least 2 intervention classes

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

7,192 participants in 2 patient groups

Treatment
Experimental group
Description:
Subjects receiving hands-on cooking and nutrition education classes
Treatment:
Behavioral: Treatment
Control
No Intervention group
Description:
Subjects not receiving any additional nutrition education aside from that contained in their curricula (for trainees) or medical care (for patients)

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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