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Effect of Rib Cage and Spine Mobility on Maximum Breath-Hold Time

S

Saglik Bilimleri Universitesi

Status

Enrolling

Conditions

Healthy Participant

Treatments

Behavioral: Sit and Reach
Behavioral: chest circumference measurement
Device: Spinal mouse (idiag m360)
Behavioral: Maximum Breath Hold Test

Study type

Observational

Funder types

Other

Identifiers

NCT05520216
21/778 (Other Identifier)
Thesis

Details and patient eligibility

About

In this study, it was aimed to look at the effect of rib cage and spine mobility on maximum breath holding time. To determine the relationship between spine and rib cage mobility level and respiratory capacity.

Full description

The demographic information of the participants (gender, age, height, body weight, body mass index, occupation, dominant extremity, education level, marital status) will be questioned with the Demographic Data Form to be created by the researchers. Except for the demographic data form, the breath-holding capacity of the participants will be evaluated by measuring the breath-holding times, and the thoracic cage mobility will be evaluated by measuring the chest circumference during normal respiration, maximal inspiration and maximal expiration. The curvature of the spine, the presence of kyphosis and lordosis will be measured using the Spinal Mouse (IDIAG m360) device, which is an objective measurement method. The flexibility of the spine and indirectly the mobility of the rib cage will be checked with the sit and lie test. The results of the evaluations will be recorded.

A consent form stating that they are healthy female and male volunteer participants aged between 18-25 years old and who meet the inclusion criteria will be filled in to participate in the study. After the consent form is signed, clinical evaluations will begin.

Study Design: Experimental nonrandomized field study

Enrollment

82 estimated patients

Sex

All

Ages

18 to 25 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Being between the ages of 18-25
  • Being cooperative
  • Those who want to participate in the study voluntarily

Exclusion criteria

  • Having had any lower extremity or spine surgery
  • Having a vestibular system disorder
  • Pregnancy or the possibility of pregnancy
  • Known, diagnosed spinal cord, visceral, or other musculoskeletal disorders
  • Refusal to participate in the study

Trial design

82 participants in 1 patient group

asymptomatic individuals
Description:
The demographic information of the participants (gender, age, height, body weight, body mass index, occupation, dominant extremity, education level, marital status) will be questioned with the Demographic Data Form to be created by the researchers. Except for the demographic data form, the breath-holding capacity of the participants will be evaluated by measuring the breath-holding times, and the thoracic cage mobility will be evaluated by measuring the chest circumference during normal respiration, maximal inspiration and maximal expiration. The curvature of the spine, the presence of kyphosis and lordosis will be measured using the Spinal Mouse (IDIAG m360) device, which is an objective measurement method. The flexibility of the spine and indirectly the mobility of the rib cage will be checked with the sit and lie test. The results of the evaluations will be recorded.
Treatment:
Behavioral: Sit and Reach
Behavioral: Maximum Breath Hold Test
Behavioral: chest circumference measurement
Device: Spinal mouse (idiag m360)

Trial contacts and locations

1

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Central trial contact

Esra PEHLİVAN

Data sourced from clinicaltrials.gov

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