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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05021068
Other study ID # IKC1233
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 1, 2018
Est. completion date March 1, 2021

Study information

Verified date August 2021
Source Izmir Katip Celebi University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

In recent studies with musculoskeletal system disorders in chronic respiratory patients, it has been reported that postural control is affected in COPD patients. The aim of this study to investigate relationship between spinal structure and mobility an severity of dyspnea in patients with COPD.


Description:

Chronic Obstructive Pulmonary Disease (COPD) is a preventable and treatable disease characterized by irreversible airway limitation. In recent studies with musculoskeletal system disorders in chronic respiratory patients, it has been reported that postural control is affected in COPD patients.It has been observed that balance systems, functional balance tests, posturography, posture assessment systems, force platform and inclinometer measurements are used in studies on postural control assessment in COPD patients.There are a limited number of studies in which devices that objectively present the degree of deviation in spinal curves are used in patients with COPD, and posture and lung volume and capacities are evaluated. Therefore, the aim of this study is to investigate the changes in spine structure and mobility in COPD patients and to reveal their relationship with static and dynamic lung volumes and capacities.


Recruitment information / eligibility

Status Completed
Enrollment 98
Est. completion date March 1, 2021
Est. primary completion date March 1, 2021
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Volunteer to participate in the study - Be over 18 years old - Being clinically stable - Not having a COPD attack in the last 3 months at least Exclusion Criteria: - Refusing to participate in the research - Having had spinal surgery Presence of back and shoulder pain - Idiopathic scoliosis - Ankylosing spondylitis - Presence of respiratory disease other than COPD - Difficulty understanding verbal commands

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Postural Assessment
Spinal mouse measurement

Locations

Country Name City State
Turkey Dr. Suat Seren Chest Diseases and Surgery Training and Research Hospital Izmir

Sponsors (1)

Lead Sponsor Collaborator
Izmir Katip Celebi University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Spinal Structure and Mobility Spinal mouse measurement 15 minutes (single application)
Secondary Pulmonary Functions Respiratory Function Test 10 minutes (single application)
Secondary Dyspnea Severity Modified Medical Research Dyspnea Scale 5 minutes (single application)
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