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NCT07226336CompletedPhase 2

Dietary Interventions to Reduce Ultra-Processed Food Intake

Testing a Dissonance-Based Intervention to Reduce Ultra-Processed Food Consumption Via Activism Against the Food Industry

Source: ClinicalTrials.gov · Last updated 15 Oct 2026

Brief summary (registry, in English)

The DISRUPT clinical trial will test two different 2-month programs to help adults with overweight/obesity (N=60) reduce their intake of ultra-processed foods (UPFs). Participants will be randomly assigned to receive standard dietary change strategies, cognitive dissonance strategies that engage them in activism against the UPF industry, or both. All participants will attend an introductory educational workshop about UPFs. If they are assigned to receive one or more of these strategies, they will attend weekly group sessions with the relevant intervention content for 7 more weeks. Groups will be held virtually.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
59 (actual)
First submitted
31 Oct 2025
Start date
10 Feb 2026
Primary completion date
31 Jul 2026
Lead sponsor
Oregon Research Institute
Diseases
Obesity
NCT number
NCT07226336

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 59
  • From 10 Feb 2026 to the primary completion date, 31 Jul 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Are using medications known to influence eating behavior and/or weight (e.g., semaglutide)
  • Currently using insulin

Other illness

  • History of bariatric surgery

Other

  • Have ever been diagnosed with anorexia nervosa or bulimia nervosa
  • Current pregnancy or planning to become pregnant during the study period

Who the study is looking for

  • Ages 18-70 years old
  • BMI \>25 and \<50 kg/m2
  • Wish to reduce their UPF intake
  • Consume at least 2 UPF items per day and at least 4 distinct UPF items per week

Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Oregon Research Institute
Coordinator of this site? Confirm its status
SpringfieldUnited StatesUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.