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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT06432062
Other study ID # 2022-13596
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date September 20, 2023
Est. completion date May 28, 2024

Study information

Verified date May 2024
Source Istanbul Saglik Bilimleri University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The rectus abdominis, which enables the trunk to flex with its activation, and the erector spinae muscles, which provide trunk extension with its activation, are among the structures located in the core region and involved in the stabilization of the spine. While the muscles in the core area actively provide the stabilization of the medulla spinalis, this stabilization is also supported by passive subsystems. Passive subsystem fascia etc. creates structures. Thoracolumbar fascia is one of the important fascias due to its connections with the muscles in the core area. Fatigue etc. of the structures in the core area. As a result of physiological processes, their functionality may decrease, which may affect the stabilization of the core area. Fatigue occurs as a result of lactic acid accumulation in the structures in the body and this process is called the recovery period. The types of exercises performed also affect the recovery period. For this reason, different exercise types such as dynamic and static can be used when creating exercise programs. Due to the functions of the rectus abdominis and erector spinae muscles and thoracolumbar fascia in the body, their effects on the spine and their connections with each other; It is aimed to examine the effect of muscle fatigue in these muscles on the viscoelastic properties of the thoracolumbar fascia and their recovery rates.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 45
Est. completion date May 28, 2024
Est. primary completion date April 15, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - Being a healthy individual between the ages of 18-35 - Not having any chronic disease - Body mass index (BMI) is 24.9 kg/m2 or lower - Volunteering to participate in the study Exclusion Criteria: - Having a chronic illness (Diabetes, blood pressure, etc.) - Having a diagnosed spine problem - Being diagnosed with scoliosis - Pilates, yoga, etc. in the last 6 months. to have done sports - Beighton score of 4 or above - Being diagnosed with cardiopulmonary system disease

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Turkey Istanbul Health Science University Istanbul Uskudar

Sponsors (1)

Lead Sponsor Collaborator
Istanbul Saglik Bilimleri University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Thoracolumbal Fascia Viscoelastic Properties Viscoelastic properties of the thoracolumbal fascia (TFL) was performed with the MyotonPRO™ (Myoton AS, Estonia) device. Before and after imeddiately after application of the fatigue protocol. The measurement point determined for TFL of individuals rest were marked with a medical marker pen. During the measurement, the probe of the device was adjusted to pulse once into the skin with a force of 0.4 N and for 15 ms. During the test, the tip of the MyotonPro™ device was placed perpendicular to the marked area and gently pressed against the skin at a depth of 3 mm until the green light came on. 2 weeks
Secondary Fatigue Assessment with Borg Scale Fatigue assessment will be made using the Modified Borg Scale. The Modified Borg Scale is a subjective evaluation method that evaluates fatigue and shortness of breath during activity or at rest between 0 and 10. 0 points "not at all" means the lowest, and 10 points "very severe" means the highest fatigue and shortness of breath. 2 weeks
Secondary Investigations of Recovery Times Moxy®, (Moxy®, Fortiori Design LLC, Minnesota, USA) Monitor will be used to detect the change in intramuscular oxygen saturation of the muscles and the time it takes to return to resting levels during and after fatigue protocols. The most swollen areas of the rectus abdominis and erector spinae muscles will be marked with a cosmetic pen and the device will be placed. 2 weeks
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