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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06296407
Other study ID # 01C319
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 8, 2023
Est. completion date December 31, 2024

Study information

Verified date February 2024
Source Istituto Auxologico Italiano
Contact Alessandro Sartorio, MD
Phone +390261911
Email sartorio@auxologico.it
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

Objectives: 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. Material and Methods: Participants: 24 males and females with obesity, aged between 12 and 18 years enrolled at the Division of Auxologia, Hospital San Giuseppe, Istituto Auxologico Italiano, IRCCS, Piancavallo (VB), Italy. The participants are subdivided randomly into two subgroups: i. one control group (12 male and female adolescents) follows the standard metabolic integrated rehabilitation protocol and ii. an experimental group (12 male and female adolescents) who, in addition to the standard protocol, performs 12 sessions (5 sessions/week for 3 weeks) of 30 minutes each of respiratory exercises. The exercise definition are based on recent studies performed on obese patients (Batrakoulis 2022 a-b; Calcaterra et al., 2013-2014) and on different patient populations where the respiratory dysfunction is a primary or secondary pathology component (Bernardi et al., 2002). All the exercises are adapted to the examined population and guided and monitored by expert staff.


Recruitment information / eligibility

Status Recruiting
Enrollment 24
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 12 Years to 18 Years
Eligibility Inclusion Criteria: - 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 Exclusion Criteria: - BMI standard deviation score (SDS) < 2; - presence of structured programs of physical activity (regular activity for more than 120min/week) for the 6 months before the study; - presence of signs/symptoms related to cardiovascular, respiratory, gastrointestinal, skeletal-muscle pathologies contraindicated for the test execution

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Standard metabolic integrated rehabilitation protocol - duration 3 weeks
Standard metabolic integrated rehabilitation protocol
Standard metabolic integrated rehabilitation protocol + respiratory exercises - duration 3 weeks
Standard metabolic integrated rehabilitation protocol + respiratory exercises (12 sessions [5 sessions/week for 3 weeks])

Locations

Country Name City State
Italy Istituto Auxologico Italiano, Site Piancavallo Oggebbio Verbania

Sponsors (1)

Lead Sponsor Collaborator
Istituto Auxologico Italiano

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fat mass Assessed by tetrapolar impedance At baseline and after 3 weeks of intervention
Primary Fat-free mass Assessed by tetrapolar impedance At baseline and after 3 weeks of intervention
Primary Maximal Inspiratory Pressure Assessed by metabolimeter At baseline and after 3 weeks of intervention
Primary Maximal Expiratory Pressure Assessed by metabolimeter At baseline and after 3 weeks of intervention
Primary Interoceptive awareness Assessed by Multidimensional Assessment of Interoceptive Awareness Scale, with a self-report survey composed of 32 items with a Likert scale composed of 5 points scale At baseline and after 3 weeks of intervention
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