The Relationship Between Hyperventilation Symptoms and Physical Performance in Obese Individuals: An Observational Study

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

Obesity has become a major public health concern worldwide due to its rapidly increasing prevalence. It is defined as an abnormal or excessive accumulation of body fat that may impair health. Obesity is associated not only with chronic conditions such as cardiovascular diseases, type 2 diabetes, osteoarthritis, and certain types of cancer, but also with impaired respiratory function. Excess body mass can reduce the range of motion of the respiratory muscles, limit the mechanical function of the chest wall and diaphragm, and decrease the efficiency of ventilation. As a result, individuals with obesity often experience exertional shortness of breath, rapid breathing, and inadequate ventilation. These symptoms may be considered part of hyperventilation syndrome, which is characterized by altered respiratory control and influenced by both physiological and psychological factors. Although some studies have reported the presence of hyperventilation symptoms in individuals with obesity, their impact on physical performance has not been adequately investigated. Hyperventilation can limit the ability to perform daily activities and may lead to fatigue, imbalance, and other problems that directly affect physical performance. The aim of this study is to examine the relationship between hyperventilation symptoms and physical performance parameters in individuals with obesity. The findings are expected to contribute to a more comprehensive assessment of physical fitness in this population and to support the development of individualized physiotherapy interventions.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
View:

• Being between 18 and 65 years of age

• Having a Body Mass Index of 30 kilograms per square meter or higher (diagnosis of obesity)

• Providing written informed consent by signing the informed volunteer consent form after receiving information about the study

• Having sufficient physical and cognitive ability to individually perform the test procedures

• Being able to read and understand the Turkish language

Locations
Other Locations
Turkey
Istinye University
RECRUITING
Istanbul
Contact Information
Primary
Kubra Kardeş, Asst. Prof.
kubra.koce@istinye.edu.tr
05387115631
Time Frame
Start Date: 2025-08-15
Estimated Completion Date: 2025-10-30
Participants
Target number of participants: 30
Treatments
Group 1
Individuals aged between 18 and 65 years, with a Body Mass Index (BMI) ≥ 30 kg/m², who have the ability to understand and respond to the questionnaires and tests used in the study.
Sponsors
Leads: Istinye University

This content was sourced from clinicaltrials.gov