Understanding dysfunctional breathing in people with Thoracic Outlet Syndrome
Investigation of the Properties of Dysfunctional Breathing in Individuals With Thoracic Outlet Syndrome
Hacettepe University · NCT06992752
This study looks at how breathing problems affect people with Thoracic Outlet Syndrome to see if there's a link between the two.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 54 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Hacettepe University (other) |
| Locations | 1 site (Ankara, Altındağ) |
| Trial ID | NCT06992752 on ClinicalTrials.gov |
What this trial studies
This observational study aims to investigate the characteristics of dysfunctional breathing patterns in individuals diagnosed with Thoracic Outlet Syndrome (TOS). Participants will be compared to a healthy control group to evaluate the association between TOS and dysfunctional breathing. The study will involve individuals aged 18-65 who have experienced pain for more than six months and have been diagnosed with TOS by a thoracic surgeon. The findings could provide insights into the respiratory challenges faced by these patients.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 18-65 diagnosed with Thoracic Outlet Syndrome and experiencing pain for over six months.
Not a fit: Patients with a history of spinal or thoracic surgery, severe obesity, or significant comorbidities may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to better understanding and management of breathing issues in patients with Thoracic Outlet Syndrome.
How similar studies have performed: While there is limited information on similar studies, the investigation of dysfunctional breathing in relation to TOS is a relatively novel approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * To agree to participate in the study, * To have been diagnosed with TOS by a thoracic surgeon, * To be between 18-65 years old, * Having pain for more than 6 months Exclusion Criteria: * Patients with a history of spinal or thoracic surgery for TOS or any other reason, * People with traumatic cervical injury, * Severely obese people (BMI \>40 kg/m2), * People with clinical abnormalities in the thoracic cage or vertebral column, * Persons with occupational industrial exposures, * Patients with severe comorbidities (neurological, neuromuscular, -cardiorespiratory, psychiatric and musculoskeletal) diabetes mellitus and/or malignancies
Where this trial is running
Ankara, Altındağ
- Hacettepe University — Ankara, Altındağ, Turkey (Türkiye) (RECRUITING)
Study contacts
- Principal investigator: Melda Sağlam, Professor — Hacettepe University
- Study coordinator: Melda Sağlam, Professor
- Email: msaglam@hacettepe.edu.tr
- Phone: +903123052525
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Thoracic Outlet Syndrome, Dysfunctional Breathing