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Inspiratory Muscle Training for Lung Transplant Recovery

N/A
Recruiting
Led By Cristiane Meirelles, PT, PhD
Research Sponsored by Ohio State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Able to ambulate pre-transplant (not bed/wheelchair bound) with or without assistive device
Be older than 18 years old
Must not have
Impaired cognition with inability to follow commands
Timeline
Screening 3 weeks
Treatment Varies
Follow Up the groups will be assessed: before lung transplantation, 8 weeks, 6 and 12 months after ltx
Awards & highlights

Summary

This trial is testing a special breathing exercise device for people who have had a lung transplant. The device helps strengthen the muscles used for breathing. The goal is to help these patients breathe better, feel less tired, and improve their ability to do everyday activities.

Who is the study for?
This trial is for people waiting for a lung transplant who can walk (even with help) and understand the study. They shouldn't have cognitive issues that make it hard to follow instructions or already be doing inspiratory muscle training.
What is being tested?
The study tests if using an inspiratory muscle trainer right after a lung transplant helps patients breathe better, feel less tired, and improve their daily activities compared to those who only get standard physical therapy.
What are the potential side effects?
Since this trial involves non-invasive breathing exercises, side effects are minimal but may include temporary increased fatigue or discomfort from the use of the training device.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I can walk by myself or with help from a device.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
Select...
I struggle to understand or follow instructions due to cognitive issues.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~the groups will be assessed: before lung transplantation, at baseline (immediate post-transplant), 8 weeks, 6 and 12 months after ltx
This trial's timeline: 3 weeks for screening, Varies for treatment, and the groups will be assessed: before lung transplantation, at baseline (immediate post-transplant), 8 weeks, 6 and 12 months after ltx for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change in fatigue: Fatigue Severity Scale
Change in functional capacity
Change in inspiratory muscle strength: Maximal inspiratory pressure (MIP) measured in cmH2O
+1 more
Secondary study objectives
Change in grip strength
Change in lower extremity muscle strength
Change in lung function: Pulmonary Function Test
+2 more

Trial Design

3Treatment groups
Experimental Treatment
Active Control
Placebo Group
Group I: Inspiratory Muscle training- Intervention groupExperimental Treatment1 Intervention
Along with standard post-transplant physical therapy, the intervention group will begin daily respiratory exercise training utilizing the IMT trainer device (POWERbreathe Medic Plus®) with weekly incremental increases in respiratory load. Patients will be asked to use the IMT device twice per day, 7 days per week, for 8 weeks.
Group II: Usual care groupActive Control1 Intervention
Patients will only participate in standard post-transplant physical therapy.
Group III: Inspiratory Muscle training - Placebo groupPlacebo Group1 Intervention
Along with standard post-transplant physical therapy, the placebo group will begin daily respiratory exercise training utilizing the IMT trainer device (POWERbreathe Medic Plus®) with no increase of respiratory load. Patients will be asked to use the IMT device twice per day, 7 days per week, for 8 weeks.

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for lung disease include bronchodilators, anti-inflammatory medications, and respiratory muscle training. Bronchodilators, such as beta agonists and muscarinic antagonists, work by relaxing the muscles around the airways, making breathing easier. Anti-inflammatory medications, like inhaled corticosteroids, reduce inflammation and swelling in the airways, improving airflow. Inspiratory muscle training (IMT) specifically targets the strengthening of respiratory muscles, enhancing their endurance and efficiency. This is particularly important for lung disease patients as it can improve exercise capacity, reduce dyspnea, and enhance overall quality of life by making daily activities less exhausting.
Inspiratory muscle training in patients with heart failure: a systematic review.Tutorial on maximum inspiratory and expiratory mouth pressures in individuals with idiopathic Parkinson disease (IPD) and the preliminary results of an expiratory muscle strength training program.

Find a Location

Who is running the clinical trial?

Ohio State UniversityLead Sponsor
859 Previous Clinical Trials
642,675 Total Patients Enrolled
Cristiane Meirelles, PT, PhDPrincipal InvestigatorSchool of Health and Rehabilitation Sciences- Physical Therapy Division

Media Library

Inspiratory Muscle training- Intervention group Clinical Trial Eligibility Overview. Trial Name: NCT05309551 — N/A
Lung Disease Research Study Groups: Inspiratory Muscle training- Intervention group, Inspiratory Muscle training - Placebo group, Usual care group
Lung Disease Clinical Trial 2023: Inspiratory Muscle training- Intervention group Highlights & Side Effects. Trial Name: NCT05309551 — N/A
Inspiratory Muscle training- Intervention group 2023 Treatment Timeline for Medical Study. Trial Name: NCT05309551 — N/A
~27 spots leftby Sep 2025