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NCT05004883Completed

Solutions for Hunger And Regulating Eating

Targeting Food Cue Responsiveness for Weight Loss

Source: ClinicalTrials.gov · Last updated 2 Nov 2026

Brief summary (registry, in English)

The objective of this proposed study is to collect efficacy data on ROC+ compared to an active comparator (AC) and to Behavioral Weight Loss (BWL) for participants who are high in Food Responsiveness.

Status (registry)
Completed
Study type
Interventional
Enrollment
293 (actual)
First submitted
6 Aug 2021
Start date
1 Sept 2021
Primary completion date
10 Jun 2026
Lead sponsor
University of California, San Diego
Diseases
Obesity
NCT number
NCT05004883

What you commit to

  • Study type: Interventional
  • Participants enrolled: 293
  • From 1 Sept 2021 to the primary completion date, 10 Jun 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

  • participating in other weight control programs and/or taking medication for weight loss
  • previous bariatric surgery

Other illness

  • major medical conditions such as diabetes or recent history of coronary heart disease; symptoms of angina, stroke, osteoarthritis, osteoporosis, orthopedic problems that would limit activity during the following 18 months; or any other serious medical condition that would make physical activity unsafe
  • bulimia or anorexia, significant cognitive impairment, a known psychotic disorder, acute suicidal ideation, moderate or severe alcohol or substance use disorder, or unstable psychiatric illness (e.g., recent psychiatric hospitalization in the past year)

Other

  • medical or psychological problems that could make adherence with the study protocol difficult or dangerous
  • pregnant, lactating, or planning to become pregnant in the next 18 months
  • moving out of the San Diego area for the duration of their study enrollment (18 months)

Who the study is looking for

  • high Food Responsiveness
  • BMI between 25kg/m\^2 and 45kg/m\^2
  • able to read English at a 5th grade reading level
  • willing and able to participate in assessment visits and treatment sessions, whether held in-person or via password protected Zoom meetings
  • able to provide data through questionnaires
  • has a smart phone through which they can complete Ecological Momentary Assessments

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
UCSD Center for Healthy Eating and Activity Research (CHEAR
Coordinator of this site? Confirm its status
La JollaUnited StatesUnknown status

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