COPD Clinical Trial
Official title:
The Effects of Creative Dance Based Exercise Training on Respiratory, Balance and Cognitive Functions, Respiratory and Peripheral Muscle Strength and Functional Capacity in Patients With Chronic Obstructive Pulmonary Disease (COPD)
Verified date | February 2021 |
Source | Bezmialem Vakif University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
COPD is a common, preventable and treatable disease associated with an increased chronic inflammatory response of the airways and lungs to harmful gases and particles and characterized by progressive airflow restriction, which is usually progressive. Exercise intolerance is one of the most important outcomes of COPD. Dyspnea and leg fatigue are the main symptoms that limit exercise and patients restrict their activity to avoid these disturbing conditions. Exercise training is the most appropriate method for improving exercise tolerance and muscle function. It is considered and recommended by ERS and ATS as an essential component of PR. Endurance training is considered to be one of the most important components of the PR program. Walking, running, cycling, stair climbing, dancing are examples of endurance exercises. Dance-based exercise training; It is an entertaining method that increases physical, functional, cognitive, emotional and social integration. This alternative method has frequently been tried in the literature in the treatment of Parkinson's, cancer and psychiatric diseases and its effects on functional capacity, balance, and quality of life have been demonstrated. The importance of our research; This is the first study to apply dance based exercise training in chronic respiratory diseases. The aim of this study was to investigate the effect of creative dance based exercise training on respiratory, balance and cognitive functions, respiratory and peripheral muscle strength and functional capacity in COPD patients.
Status | Completed |
Enrollment | 24 |
Est. completion date | January 31, 2021 |
Est. primary completion date | January 31, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Having FEV1 / FVC <70% from pulmonary function test - Being older than 18 years - To be able to read and understand Turkish Exclusion Criteria: - No exacerbation in 8 weeks. - Attending current or regular exercise training in the last 1 year - Having diagnosed vision, hearing, vestibular or neurological problems that may affect balance - Having orthopedic, musculoskeletal or cardiovascular comorbid conditions that may affect ambulation - Being on long-term oxygen therapy |
Country | Name | City | State |
---|---|---|---|
Turkey | Bezmialem Vakif University, Department of Physiotheraphy and Rehabilitation | Istanbul |
Lead Sponsor | Collaborator |
---|---|
Bezmialem Vakif University |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Respiratory Function Test | Change from baseline forced vital capacity (FVC) at 8 weeks. | Eight weeks | |
Primary | Respiratory Function Test | Change from baseline forced forced expiratory volume in 1 second at 8 weeks. | Eight weeks | |
Primary | Respiratory Function Test | Change from baseline peak expiratory flow (PEF) at 8 weeks. | Eight weeks | |
Primary | COPD Assessment Test (CAT) | Change from baseline CAT score at 8 weeks. | Eight weeks | |
Primary | BODE Index | Change from baseline BODE score at 8 weeks. | Eight weeks | |
Primary | Balance | Change from baseline postural stability test score in BIODEX Balance System at 8 weeks. | Eight weeks | |
Primary | Balance | Change from baseline limits of stability test score in BIODEX Balance System at 8 weeks. | Eight weeks | |
Primary | Respiratory Muscle Strength | Change from baseline maximum inspiratory pressure at 8 weeks. | Eight weeks | |
Primary | Respiratory Function Test | Change from baseline maximum expiratory pressure at 8 weeks. | Eight weeks | |
Primary | Functional Capacity | Change from baseline distance covered in six minute walk test at 8 weeks. | Eight weeks | |
Primary | Change from baseline handgrip strength at 8 weeks. | Change from baseline m. quadriceps strength at 8 weeks. | Eight weeks | |
Primary | Change from baseline handgrip strength at 8 weeks. | Change from baseline m. biceps strength at 8 weeks. | Eight weeks | |
Primary | Change from baseline handgrip strength at 8 weeks. | Change from baseline handgrip strength at 8 weeks. | Eight weeks |
Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
NCT06000696 -
Healthy at Home Pilot
|
||
Active, not recruiting |
NCT03927820 -
A Pharmacist-Led Intervention to Increase Inhaler Access and Reduce Hospital Readmissions (PILLAR)
|
N/A | |
Completed |
NCT04043728 -
Addressing Psychological Risk Factors Underlying Smoking Persistence in COPD Patients: The Fresh Start Study
|
N/A | |
Completed |
NCT04105075 -
COPD in Obese Patients
|
||
Recruiting |
NCT05825261 -
Exploring Novel Biomarkers for Emphysema Detection
|
||
Active, not recruiting |
NCT04075331 -
Mepolizumab for COPD Hospital Eosinophilic Admissions Pragmatic Trial
|
Phase 2/Phase 3 | |
Terminated |
NCT03640260 -
Respiratory Regulation With Biofeedback in COPD
|
N/A | |
Recruiting |
NCT04872309 -
MUlti-nuclear MR Imaging Investigation of Respiratory Disease-associated CHanges in Lung Physiology
|
||
Recruiting |
NCT05145894 -
Differentiation of Asthma/COPD Exacerbation and Stable State Using Automated Lung Sound Analysis With LungPass Device
|
||
Withdrawn |
NCT04210050 -
Sleep Ventilation for Patients With Advanced Hypercapnic COPD
|
N/A | |
Terminated |
NCT03284203 -
Feasibility of At-Home Handheld Spirometry
|
N/A | |
Recruiting |
NCT06110403 -
Impact of Long-acting Bronchodilator- -Corticoid Inhaled Therapy on Ventilation, Lung Function and Breathlessness
|
Phase 1/Phase 2 | |
Active, not recruiting |
NCT06040424 -
Comparison of Ipratropium / Levosalbutamol Fixed Dose Combination and Ipratropium and Levosalbutamol Free Dose Combination in pMDI Form in Stable Chronic Obstructive Pulmonary Disease (COPD) Patients
|
Phase 3 | |
Recruiting |
NCT05865184 -
Evaluation of Home-based Sensor System to Detect Health Decompensation in Elderly Patients With History of CHF or COPD
|
||
Recruiting |
NCT04868357 -
Hypnosis for the Management of Anxiety and Breathlessness During a Pulmonary Rehabilitation Program
|
N/A | |
Completed |
NCT01892566 -
Using Mobile Health to Respond Early to Acute Exacerbations of COPD in HIV
|
N/A | |
Completed |
NCT04119856 -
Outgoing Lung Team - a Cross-sectorial Intervention in Patients With COPD
|
N/A | |
Completed |
NCT04485741 -
Strados System at Center of Excellence
|
||
Completed |
NCT03626519 -
Effects of Menthol on Dyspnoea in COPD Patients
|
N/A | |
Recruiting |
NCT04860375 -
Multidisciplinary Management of Severe COPD
|
N/A |