Inspiratory Muscle Training Efficiency Before Bronchoscopic Procedure

Saglik Bilimleri Universitesi

Status: Completed

Conditions: IMT; Copd

Treatments: Other: Standard pulmonary rehabilitation programme; Other: Inspiratory muscle training

Study type: Interventional

Funder types: Other

Identifiers

NCT05540054

BLVR_IMT

Details and patient eligibility

About

The aim of this study is to examine the effectiveness of inspiratory muscle training (IMT) before bronchoscopic procedure in Chronic Obstructive Pulmonary Patients (COPD). Patients with a diagnosis of COPD, who are listed for a bronchoscopic procedure and referred to the pulmonary rehabilitation (PR) clinic, will be randomly divided into two groups. Standard PR exercise program will be applied to both groups. In addition to the standard program, IMT will be applied to one of the groups. The effect of IMT on exercise program gains will be examined.

Full description

• Cases diagnosed with COPD by a chest diseases specialist at Yedikule Chest Diseases and Thoracic Surgery Training and Research Hospital will be included in the study.
• The cases meeting the inclusion criteria will be randomized and divided into two groups, called the standard rehabilitation group (PRGr) and the inspiratory muscle training group (IMTGr).
• Initial exercise sessions and all evaluations of all cases will be performed in the hospital. The 2nd and 3rd training repetitions will be held at their homes via online synchronized videoconferencing. The exercise video will be sent to the smart phones of the cases who have completed 3 training sessions. Participants will be called once a week by phone and exercise follow-up will be carried out.
• All subjects will continue to exercise 5 days a week for 2 months. The standard PR consists of breathing exercises, peripheral muscle strength and self walking training. In addition, IMT was applied to IMTGr.

Enrollment: 64 patients

Sex: All

Ages: 18 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Being between the ages of 18-75
• Having a diagnosis of COPD diagnosed according to clinical diagnostic criteria according to -American Thoracic and European Respiratory Societies (ATS-ERS) and being a candidate patient for bronchoscopic lung volume reduction procedure
• Presence of dyspnea on exertion
• Stable clinical state at the time of inclusion without infection or exacerbation in the previous 4 weeks
• Ability to use a smart phone

Exclusion criteria

• Patients with severe comorbid diseases, unstable coronary artery disease, collagen vascular diseases and needing high flow oxygen therapy (˃ 3-4 L \min).
• A history of effort-related syncope or any comorbidity (such as severe orthopedic or neurological deficits or unstable heart disease) that precludes exercise training.
• Participation in a pulmonary rehabilitation program within the past 12 months.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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64 participants in 2 patient groups

Standard pulmonary rehabilitation group (PR)

Experimental group

Description:

Patients diagnosed with COPD and listed for bronchoscopic procedure.

Treatment:

Other: Standard pulmonary rehabilitation programme

Inspiratory muscle training group (PR+IMT)

Experimental group

Description:

Patients diagnosed with COPD and listed for bronchoscopic procedure.

Treatment:

Other: Inspiratory muscle training

Other: Standard pulmonary rehabilitation programme