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NCT07627256Not yet recruiting

Weight Loss Composition and Metabolic Adaptation During Hypocaloric Dieting

The Relationship Between Weight Loss Composition, Body Composition Changes, and Metabolic Adaptation During a Hypocaloric Dietary Intervention

Source: ClinicalTrials.gov · Last updated 8 Oct 2026

Brief summary (registry, in English)

Weight loss induced by hypocaloric dietary interventions is commonly accompanied by reductions in resting metabolic rate (RMR), a phenomenon often described as metabolic adaptation. The magnitude of this decline varies substantially between individuals and may depend not only on the amount of weight lost but also on the composition of weight loss, particularly the relative contributions of fat mass and fat-free mass. This prospective interventional study will investigate whether changes in body composition during a hypocaloric dietary intervention are associated with changes in RMR and metabolic adaptation. Approximately 150 adults with overweight or obesity will participate in a structured dietary program designed to induce moderate energy restriction. Body composition and resting metabolic rate will be assessed before and after the intervention to evaluate associations between fat mass loss, fat-free mass loss, and metabolic responses to weight reduction.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
150 (estimated)
First submitted
31 May 2026
Start date
1 Dec 2026
Primary completion date
31 Dec 2027
Lead sponsor
Tel Aviv University
Diseases
Obesity
NCT number
NCT07627256

What you commit to

  • Study type: Interventional
  • Planned participants: 150
  • From 1 Dec 2026 to the primary completion date, 31 Dec 2027
  • No sites listed in no 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

  • Use of medications known to substantially affect metabolism or body composition.

Other illness

  • Diagnosed metabolic or endocrine disorders known to affect energy expenditure.
  • Any medical condition that, in the opinion of the investigators, precludes safe participation.

Other

  • Pregnancy or breastfeeding.

Who the study is looking for

  • Adults aged 18 years and older.
  • Individuals living with overweight or obesity.
  • Willingness and ability to comply with dietary recommendations and study procedures.
  • Provision of written informed consent.

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

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