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NCT06299254Completed

Placebo Effect About Fatigue in Obesity

The Modulation of Individual Level of Fatigue Through Placebo Effect in Obesity

Source: ClinicalTrials.gov · Last updated 27 Aug 2025

Brief summary (registry, in English)

Fatigue is a central symptom of obesity: it significantly impacts daily functioning, psychological well-being, compliance with physical therapy, and quality of life. However, the full understanding of the origin and treatment of fatigue in obesity is still a matter of debate, requiring further research, especially from new perspectives. From a neuroscientific perspective, fatigue is more than the subjective perception of tiredness resulting from mental or physical exertion or illness. It results in the complex interaction between (bottom-up) sensory input coming from the periphery, and motivational and psychological input, which is related to top-down cognition. In this framework, placebos may affect the output of the top-down cognitive processing by altering the individual evaluation of the ongoing peripheral performance. Indeed, evidence from both healthy conditions and clinical contexts suggests that fatigue can be modulated. The after-effect of such a modulation can be observed not only at a behavioural level, in terms of physical endurance, but also a psychological (i.e., decreased of perceived fatigue) and neurophysiological (changes in brain activity, especially in the fatigue-related components as the RP) levels.

Status (registry)
Completed
Study type
Observational
Enrollment
80 (actual)
First submitted
28 Feb 2024
Start date
1 Mar 2023
Primary completion date
28 Feb 2025
Lead sponsor
Istituto Auxologico Italiano
Diseases
Obesity
NCT number
NCT06299254

What you commit to

  • Study type: Observational
  • Participants enrolled: 80
  • From 1 Mar 2023 to the primary completion date, 28 Feb 2025
  • 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

  • concurrent neurological, neurodevelopmental (e.g., autism), motor, somatosensory and/or psychiatric disorders

Who the study is looking for

  • Right-handed diagnosis of obesity (the level of body mass index - BMI - higher or equal to 30).

Age in the registry: 20 years to 50 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
IRCCS Istituto Auxologico Italiano - Ospedale San Giuseppe
Coordinator of this site? Confirm its status
PiancavalloItalyUnknown status

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