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Effectiveness of Respiratory Muscle Training with a Mobile Application After Lobectomy

Evaluation of the Effectiveness of Respiratory Muscle Training with a Mobile Application in the Early Postoperative Period After Lobectomy

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06813144
Enrollment
45
Registered
2025-02-06
Start date
2025-03-01
Completion date
2026-02-01
Last updated
2025-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer (NSCLC), Respiratory Muscle, Thoracic Surgery, Video Assisted Thoracic Surgery (VATS)

Keywords

lung cancer, vats, inspiratory muscle training

Brief summary

It has been observed that there are negative effects on respiratory muscle strength following lobectomy. This has led to the necessity of respiratory muscle training to mitigate these adverse effects. Most studies conducted so far focus on the late postoperative period, and there are only a few studies evaluating the effectiveness of early postoperative inspiratory muscle training (IMT). It is believed that this method could be useful for facilitating patient follow-up and increasing patient motivation through visual feedback.

Detailed description

It has been observed that there are negative effects on respiratory muscle strength following lobectomy. This has led to the necessity of respiratory muscle training to mitigate these adverse effects. Most studies conducted so far focus on the late postoperative period, and there are only a few studies evaluating the effectiveness of early postoperative inspiratory muscle training (IMT). Additionally, there is currently no study assessing the effectiveness of IMT using a smart adapter in patients who have undergone lobectomy. It is believed that this method could be useful for facilitating patient follow-up and increasing patient motivation through visual feedback. The aim of this study is to examine the changes in respiratory muscle strength and exercise capacity in patients after lobectomy via VATS, comparing classical IMT, mobile application-supported IMT, and a control group that does not receive IMT.

Interventions

Inspiratory muscle training will be given with or without smart adaptor.

Sponsors

Hacettepe University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

double blind (participant and statistician)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Volunteering to participate in the study, * Being clinically stable, * Being a lung cancer patient with a planned lobectomy with VATS, * Being between the ages of 18-65, * Being able to cooperate with the tests to be performed.

Exclusion criteria

* Having any orthopedic or neurological problem that prevents walking, * Having undergone any surgery related to the thoracic wall, * Having diseases that will affect respiratory parameters such as severe heart failure, severe chronic obstructive pulmonary disease (COPD).

Design outcomes

Primary

MeasureTime frameDescription
Inspiratory muscle strengthMeasurements will be performed before surgery (the day before surgery), at discharge and during the follow-up period after surgery (10-15 days after discharge).Respiratory muscle strength will measure by measuring mouth pressure and using maximal inspiratory pressure (MIP) values.
Expiratory muscle strengthMeasurements will be performed before surgery (the day before surgery), at discharge and during the follow-up period after surgery (10-15 days after discharge).Respiratory muscle strength will measure by measuring mouth pressure and using maximal expiratory pressure (MEP) values.

Secondary

MeasureTime frameDescription
Exercise MotivationThe evaluation will be made during the control period (10-15 days after discharge).Exercise Motivation Attitude Scale will be used. This scale consists of 3 sub-dimensions (negative attitude and thought/positive view and health/physical appearance and health).
Dyspnea LevelAn evaluation will be made in the preoperative (the day before surgery) and control period (10-15 days after discharge).Modified Borg Scale will be used to evaluate dyspnea.
Functional exercise capacityEvaluations will be made before surgery (the day before surgery) and during the follow-up period (10-15 days after discharge).6-minute walk test (6MWT) will be used to evaluate functional exercise capacity.
Physical PerformanceEvaluations will be made in the preoperative (the day before surgery) and control (10-15 days after discharge) periods.The Short Physical Performance Battery, a frequently used test in cardiovascular and pulmonary diseases, will be used.
Quality of LifeThe evaluation will be made during the preoerative (the day before surgery) and control (10-15 days after discharge) period.SF-12 Quality of Life Scale will be used to assess quality of life.
Postoperative Pulmonary ComplicationsPostoperative first-fifth days.Postoperative pulmonary complications will be evaulate by Melbourne Group Scale. If more than 4 parameters are positive, it will be considered as having postoperative pulmonary complication.

Countries

Turkey (Türkiye)

Contacts

Primary ContactFunda Alma, MsC
fundasirakaya@outlook.com+905079394348
Backup ContactEbru Calik Kutukcu, Professor
ebru.calik@hacettepe.edu.tr+905442850087

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026