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The Effects of Telerehabilitation in Patients With COPD

K

Kırıkkale University

Status

Unknown

Conditions

COPD

Treatments

Other: Treatment

Study type

Interventional

Funder types

Other

Identifiers

NCT04879576
KKUniversity

Details and patient eligibility

About

Chronic Obstructive Pulmonary Disease is a serious public health problem worldwide and it is a leading cause of mortality and morbidity. Nowadays, COPD patients are increasing in all societies and the problems that arise during the life of these patients increase the need for care and rehabilitation. Pulmonary rehabilitation has proven to be the best supportive treatment for individuals with COPD. However, there are difficulties in rehabilitation practices in terms of the fragility of patients, transportation and access problems. Telerehabilitation allows patients who cannot access rehabilitation due to their geographical, economic or physical disabilities to benefit from rehabilitation services. There are different studies demonstrating the effect of telerehabilitation in COPD patients and confirming that it is safe, but it is a developing area and has a limited area of use.

In this randomized controlled study, it is aimed to examine the effect of telerehabilitation training on respiratory functions, exercise capacity, quality of life, fatigue and psychosocial factors in individuals with COPD via video conferencing including respiratory exercises and postural exercises.

Enrollment

30 estimated patients

Sex

All

Ages

40 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Having been diagnosed with chronic obstructive pulmonary disease according to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) criteria
  • Not having an attack in the last 2 months
  • Volunteering to participate in the study
  • Being between the ages of 40-80
  • To have a device that can be used in telerehabilitation application and an active internet connection.

Exclusion criteria

  • Unstable angina, previous myocardial infarction, severe congestive heart failure resistant to medical therapy, uncontrolled hypertension, cancer, neurological or musculoskeletal disorders with functional limitations
  • Currently addicted to alcohol or drugs
  • Having an injury to the lower extremity such as sprains, sprains or fractures in the last 6 months, not being able to perform independent ambulation
  • Having serious vision and hearing problems
  • Having severe cognitive impairment

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 2 patient groups

Treatment Group
Experimental group
Treatment:
Other: Treatment
Control Group
No Intervention group

Trial contacts and locations

1

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Central trial contact

Beyza Karakaş

Data sourced from clinicaltrials.gov

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