Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID07225881

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

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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

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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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