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NCT Number: NCT06573255

Assessment of Cardiopulmonary Fitness in Healthy Adults

This project was aimed to investigate cardiorespiratory fitness and the factors affecting cardiorespiratory fitness in healthy adults. The data obtained with this project will be normative values for the data obtained with CPET in healthy people.

Recruiting

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Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Hacettepe University

Ankara, Turkey (Türkiye)

Location status: Recruiting

Location contact

Aslıhan Cakmak Onal, PhD

SUB_INVESTIGATOR

Aydan Asli Aksel Uylar, MSc

SUB_INVESTIGATOR

Aynur Demirel, PhD

SUB_INVESTIGATOR

Deniz İnal İnce, PhD

SUB_INVESTIGATOR

Ebru Calik Kutukcu

CONTACT

[email protected]

3123051576 ext. 178

Ebru Calik Kutukcu, PhD

PRINCIPAL_INVESTIGATOR

Melda Saglam, PhD

SUB_INVESTIGATOR

Naciye Vardar Yagli, PhD

SUB_INVESTIGATOR

About this study

Cardiorespiratory fitness is one of the 'health-related physical fitness' components of physical fitness and can be expressed as 'the ability of the heart, lung and vascular system to deliver oxygen and nutrients to working muscles'. Cardiopulmonary exercise testing (CPET) is a common procedure used to assess cardiopulmonary fitness, identify physiological factors limiting exercise, identify potential therapeutic targets for these factors, and evaluate the effects of an intervention. Therefore, in this project, it was aimed to investigate cardiorespiratory fitness and the factors affecting cardiorespiratory fitness in healthy adults. The data obtained with this project will be normative values for the data obtained with CPET in healthy people.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18-65 years of age,
  • Volunteering to participate in the study,
  • Co-operation,
  • Being able to ambulate.

Exclusion criteria

  • Having any known respiratory, cardiac, neurological or other internal disease or malignant disease,
  • Having any problem or musculoskeletal system disorder that prevents walking,
  • To have undergone any surgery within the last six months

Treatment and study plan

Healthy group

Other

Cardiopulmonary exercise test, respiratory function tests, respiratory muscle strength and physical activity assessment will be performed in this group.

Primary outcomes

  1. Cardiorespiratory Fitness

    Time frame: This test takes 15 to 20 minutes.

    In this parameter, which is assessed by cardiopulmonary exercise testing, the oxygen consumption measured during the test and the workload achieved in the test will be taken into consideration.

Secondary outcomes

  1. Respiratory Function Test

    Time frame: This test takes 3 to 5 minutes.

    The pulmonary function test is a test that assesses respiratory function by performing certain manoeuvres.

  2. Respiratory Muscle Strength Test

    Time frame: This test takes 3 to 5 minutes.

    Inspiratory and expiratory muscle strengths will be measured separately by breathing manoeuvres.

  3. Physical Activity

    Time frame: This questionnaire takes 1 minute.

    Physical activity level will be measured with International Physical Activity Questionnaire.

Study contacts

Contact information is provided by the study sponsor or research team.

Ebru Calik Kutukcu, PhD

CONTACT

[email protected]

3123051576

Sponsors and collaborators

Lead sponsor

Hacettepe University

Other

Registry information

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Aug 27, 2024
Registry last updated
Aug 27, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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