Actively Recruiting
Efficacy of a Multi-level Intervention to Promote Adherence to WCRF/AICR Dietary Guidelines for Cancer Prevention
Led by Drexel University · Updated on 2026-03-16
472
Participants Needed
1
Research Sites
25 weeks
Total Duration
On this page
Sponsors
D
Drexel University
Lead Sponsor
N
National Institutes of Health (NIH)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating a multi-level intervention designed to help adults improve their diet according to the World Cancer Research Fund/American Institute for Cancer Research (WCRF/AICR) guidelines to reduce cancer risk. This study will enroll 472 adults from the community, including index participants and their household members, who currently have low adherence to dietary guidelines focused on increasing fruits, vegetables, and whole grains while reducing processed foods, red and processed meat, and sugary drinks. The study aims to test whether the "Eatwell" intervention leads to better dietary adherence and improved inflammation markers compared to traditional nutrition education. Participants will be randomly assigned to one of two groups. The Eatwell group will receive an 18-month program including 12 workshop sessions focused on healthy grocery shopping, eating at home to benefit from healthier defaults, and handling temptations when eating out. Household members will join four of these sessions to support the index participant. The comparison group will receive traditional nutrition education with the same number and schedule of sessions but without the additional motivation and self-regulation content, and household members in this group will not participate in the intervention. During the study, participants will attend scheduled workshops and complete assessments at baseline, 6 months, and 18 months, including dietary adherence scoring and biomarker measurements related to inflammation through blood draws at partnered commercial laboratories. Researchers will measure changes in dietary patterns and inflammation markers, track adherence using standardized scoring, and evaluate how household support influences outcomes. The study includes ongoing monitoring and the total participation is expected to last 18 months.
CONDITIONS
Brief Title
Eatwell Clinical Trial (R01)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 or older
- Access to technology to receive emails and join videoconferencing meetings
- Ability to read and speak English
- Willingness to be randomized to either study condition and attend intervention sessions
- Willingness to serve in a support role if assigned to Eatwell condition
- Ability to have blood drawn at partnered commercial laboratory during study visits
- Low adherence to WCRF/AICR dietary guidelines (score of 2 or less on dietary adherence)
- Share a household with an adult who consents, meets eligibility, and plans to stay in household for 18 months
- Agree not to join another intervention study by this team in next 18 months
- Completion of enrollment and baseline data tasks by self and household member
- Have and regularly check an email for study communication
- Baseline weight 396 lbs or less due to scale limitations
You will not qualify if you...
- Medical or psychiatric condition that limits ability to follow dietary recommendations
- History of anorexia nervosa or bulimia nervosa
- Psychiatric condition that limits household member's support role
- Taking medication that significantly changes appetite or eating, including GLP-1 medications
- Planning to join another lifestyle modification program in next 18 months
- History of bariatric surgery
- Currently pregnant or planning pregnancy in next 18 months
- Diagnosis of Type 1 Diabetes
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 18 months
Participants receive either the Eatwell intervention or traditional nutrition education through a series of 12 workshop sessions focused on improving dietary habits for cancer prevention.
12 workshop sessions over 18 months; initial 4 sessions weekly in Month 1, then less frequent
Trial Site Locations
Total: 1 location
1
Drexel University
Philadelphia, Pennsylvania, United States, 19104
Actively Recruiting
Research Team
R
Research Coordinator, BA
M
Meghan L Butryn, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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