Determination of Body Awareness and the Functional Movement in Patients With COPD

NCT ID: NCT06298994

Last Updated: 2024-03-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

60 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-03-08

Study Completion Date

2026-03-08

Brief Summary

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The aim of this study is to investigate body awareness and functional movement in patients with Chronic Obstructive Pulmonary Disease (COPD) compared to healthy controls.

Detailed Description

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It is aimed at investigating body awareness, and functional movement, and related factors in patients with COPD. The secondary purpose is to determine correlations between body awareness and functional movement, respiratory muscle strength and endurance, daily living activities, posture, and pain threshold in this study. The determination of correlations between functional movement, respiratory pattern, and functional exercise capacity is also purposed. In accordance with these purposes, at least 30 patients with COPD will be included and at least 30 healthy controls will be included. Tests and questionnaires will be used in order to determine the severity of disease. Lung function test and respiratory muscle strength and endurance test will be performed. Six Minute Walk Test will be performed for functional exercise capacity. To evaluate posture, the Corbin Postural Assessment Scale will be used. Pain and pain threshold will be assessed via Visual Analog Scale and an algometer, respectively. Body Awareness Rating Questionnaire will be used for evaluating body awareness. To evaluate daily living activities, Glittre Activities of Daily Living Test will be used. The Functional Movement Screen Test will be used for functional movement analysis. According to the results to be obtained, body awareness and functional movement will be determined in patients with COPD. It will guide professional working in this field.

Conditions

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Pulmonary Disease, Chronic Obstructive Postural; Defect Movement, Abnormal Pain

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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study group

Patients with Chronic Obstructive Pulmonary Disease

No interventions assigned to this group

control group

Aged-matched healthy controls

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Being under 55 years old
* To be literate,
* Having volunteered to participate in the research,
* Stage 1-2-3-4 according to the Classification of Airflow Limitation in COPD (GOLD) system,
* Being clinically stable for the last 2 weeks.


* Not having any cardiopulmonary system disease or chronic systemic disease,
* To be literate,
* Being under 55 years old
* Be willing to participate in the study.
* Not having balance problems, musculoskeletal, neurological and psychiatric disorders that could prevent performing the test procedures.

Exclusion Criteria

* Having history of lung cancer, sarcoidosis, tuberculosis and/or lung surgery,
* Communication problems,
* Having a severe psychiatric disorder.
Minimum Eligible Age

18 Years

Maximum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Hacettepe University

OTHER

Sponsor Role lead

Responsible Party

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Aynur Demirel

Principal investigator; PT, PhD, Assoc. Prof.

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Aynur Demirel

Ankara, , Turkey (Türkiye)

Site Status

Hacettepe University

Ankara, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Central Contacts

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Aynur Demirel, PhD

Role: CONTACT

+905545295057

Hidaye Yamikan, PT,MSc

Role: CONTACT

+905349898724

Facility Contacts

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Aynur Demirel

Role: primary

+905545295057 ext. 178

hidaye yamikan

Role: backup

+905349898724

Other Identifiers

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SBA 23/391

Identifier Type: -

Identifier Source: org_study_id

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