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Study identifier: NCT06931730 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Reprogramming Energy Homeostasis in Overweight Individuals Via Exercise, Cognitive, and Social Training

Condition: Obesity and Overweight · Leptin Resistance · Childhood Obesity  ·  Sponsor: Bambino Gesù Hospital and Research Institute

PhaseNA
Planned participants240
Who can joinAll sexes, 6 Years to 11 Years
Healthy volunteersNo

About this study

The RESILIENT project is a clinical trial investigating leptin sensitivity in both children and adults with overweight or obesity. The study examines the additive effects of Cognitive Training (CT) and Social Training (ST) on leptin sensitivity, compared to stand-alone Intensive Health Behaviour Treatment (IHBT), which includes diet and Physical Activity (PA). The intervention will last for 8 weeks, followed by a 12-week washout period. A multilevel assessment will be conducted, evaluating in vivo leptin sensitivity (through the ratio of leptin levels to caloric intake) as well as ex vivo molecular analysis of leptin signaling in Peripheral Blood Mononuclear Cells (PBMCs). Additionally, clinical, psychological, cognitive, and physiological assessments will be performed to assess the efficacy of each intervention. By investigating leptin resistance as a potential molecular bridge between metabolic dysregulation and cognitive dysfunctions, this study may contribute to the development of more effective, long-term treatments for obesity and overweight. Additionally, in vivo investigation of leptin sensitivity may be particularly important for providing evidence of the metabolic and cognitive effects necessary for developing novel anti-obesity treatments.

This description comes directly from the study's public registry record.

Talk to the study team

Melania Manco  ·  +39 3317775547  ·  melania.manco@opbg.net

Always discuss trial participation with your own doctor first.

Locations (2)

Ospedale Pediatrico Bambino GesùRome, Italy, ItalyRecruiting
Bambino Gesù Hospital and Research Institute,Rome, Rome, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT06931730