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NCT05203718Completed

The Retrain Your Brain for Healthy Eating Study

A Mixed Methods, Single-group, Single-center Feasibility Study of a Food Response Training to Reduce Unhealthy Dietary Intake and Promote Weight Loss in Racially and Ethnically Diverse Patients With Obesity

Source: ClinicalTrials.gov · Last updated 25 May 2025

Brief summary (registry, in English)

The aim of this mixed methods, single-group, single-center study will be to examine the feasibility of a food response training (FRT). This study will be conducted in patients with obesity recruited from NYU Langone Health. Measurements will occur at screening, baseline, and 3 months, for a subgroup of participants for we will collect saliva samples for genetic analysis at baseline assessment (ancillary study).

Status (registry)
Completed
Study type
Interventional
Enrollment
35 (actual)
First submitted
20 Jan 2022
Start date
9 Nov 2022
Primary completion date
9 Apr 2025
Lead sponsor
NYU Langone Health
Diseases
Obesity
NCT number
NCT05203718

What you commit to

  • Study type: Interventional
  • Participants enrolled: 35
  • From 9 Nov 2022 to the primary completion date, 9 Apr 2025
  • 2 sites 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

  • have had bariatric surgery within the past 2 years
  • unwilling to delay bariatric surgery for the next 6 months
  • who have gained or loss more than 5.5 kg in the previous 3 months

Other illness

  • taking any medication that may impact dietary intake and weight:
    • Immunosuppressants, steroids, medications for weight loss or to manage blood sugars or a psychiatric condition other than anxiety/depression
  • unable to participate meaningfully in an intervention that involves using software available in English. The reason for this is that the food training apps have not been designed or validated in audio form or in other languages. (e.g., due to uncorrected sight impairment, illiterate, non-English-speaking, dementia)

Other

  • pregnant or breastfeeding or plan to become pregnant in the next 6 months, or who become pregnant during the study
  • enrolled in another intervention that could influence dietary intake
  • institutionalized (e.g., in a nursing home or personal care facility, or those who are incarcerated and have limited control over diet), unwilling or inability to provide informed consent.

Who the study is looking for

  • ≥18 to 80 years of age
  • BMI ≥30.0 kg/m2
  • access to a computer or an iPhone/iPad or be willing to use a study loaner smart phone

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

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

SiteCityCountrySite status
NYU Langone Health
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
NYU Clinical & Translational Science Institute Clinical Research Center (CTSI CRC)
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status

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