Life sciences · Interventional Study
ClinicalTrials.gov · October 1, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Interventional Study.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
This record has not been graded across any dimension yet. Treat the label above as provisional and read the source.
What is missing. This record has no bottom line, key findings, reported figures, evidence dimensions. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT05177705). This is a study registration, not published results. Lead sponsor: State University of New York at Buffalo. Recruitment status: COMPLETED. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 126 participants (ACTUAL). Conditions: Pediatric Obesity, Nutrition Disorders, Binge Eating, Body Weight. Interventions: BEHAVIORAL: Restricted access task; BEHAVIORAL: Structured Intake. Primary outcome measures: Overall kcal and STUDY Food kcal Consumed After the Intervention Conditions (Behavioral Restriction and Structured Intake) , Visit 3 (day 21) and visit 4 (day 42); Overall Macronutrients Consumed After the Intervention Conditions (Behavioral Restriction and Structured Intake) , Visit 3 (day 21) and visit 4 (day 42). Brief summary: This study aims to determine the relationships among loss of control eating, restriction, relative reinforcing value of high energy-dense food, and obesity risk. In order to achieve this aim, the investigators will follow children over the course of a year, obtaining behavioral and observational measurements, in addition to a two-week restricted access and two week non-restricted access period.