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NCT06296407Completed

Psychophysical Analysis of Adolescent Patients With Obesity and Efficacy of the Respiratory Approach (PSICOFISADOLOB).

Integrated Psychophysical Analysis of Adolescent Patients With Obesity and Efficacy of the Respiratory Approach in Promoting the Condition of Psychophysical Well-being and the Performance of Physical Activity

Source: ClinicalTrials.gov · Last updated 30 Apr 2025

Brief summary (registry, in English)

Specifically, the project aims to pursue the following objectives: 1. To evaluate in male and female adolescents with obesity the interaction between different psycho-body aspects such as respiration - posture - self-perception and affectivity and tolerance to physical exercise; 2. To evaluate in a subgroup of male and female adolescents the effectiveness of exercises aimed at respiratory muscles and of respiratory consciousness on the parameters above indicated and on their interaction. The final objective of this project is to define and propose "take home" specific respiratory exercises to promote greater body awareness and a condition of psychophysical well-being stable over time, creating a condition that can favor further interventions on obesity. Finally, the project aims to build solid scientific bases to insert respiratory exercise among the intervention guidelines to prevent and reduce obesity, particularly youth obesity.

Status (registry)
Completed
Study type
Interventional
Enrollment
24 (actual)
First submitted
29 Feb 2024
Start date
8 Aug 2023
Primary completion date
31 Jul 2024
Lead sponsor
Istituto Auxologico Italiano
Diseases
Obesity
NCT number
NCT06296407

What you commit to

  • Study type: Interventional
  • Participants enrolled: 24
  • From 8 Aug 2023 to the primary completion date, 31 Jul 2024
  • 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

  • presence of structured programs of physical activity (regular activity for more than 120min/week) for the 6 months before the study;

Other

  • BMI standard deviation score (SDS) \< 2;
  • presence of signs/symptoms related to cardiovascular, respiratory, gastrointestinal, skeletal-muscle pathologies contraindicated for the test execution

Who the study is looking for

  • BMI standard deviation score (SDS) \> 2;
  • absence of structured programs of physical activity (regular activity for more than 120min/week) for the 6 months before the study;
  • absence of signs/symptoms related to cardiovascular, respiratory, gastrointestinal, skeletal-muscle pathologies contraindicated for the test execution

Age in the registry: 12 years to 18 years · Sex: All · Does not accept 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
Istituto Auxologico Italiano, Site Piancavallo
Coordinator of this site? Confirm its status
OggebbioItalyUnknown status

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