- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07646288
Acute Effects of Visual Feedback-Assisted Inspiratory Muscle Training After Lobectomy
Evaluation of the Acute Effects of Respiratory Muscle Strength Training With Visual Feedback in Lung Cancer Patients Undergoing Lobectomy
Studienübersicht
Status
Bedingungen
Detaillierte Beschreibung
Lung cancer is one of the leading causes of cancer-related mortality worldwide. In patients with early-stage non-small cell lung cancer, surgical resection remains the main curative treatment option. Lobectomy, particularly through video-assisted thoracic surgery, is commonly performed as an anatomical resection method. However, despite the advantages of minimally invasive thoracic surgery, patients may experience postoperative pulmonary complications, impaired respiratory muscle function, pain-related breathing limitations, and reduced exercise capacity after lobectomy.
Inspiratory muscle training is commonly used as part of postoperative physiotherapy and pulmonary rehabilitation after thoracic surgery. Because inspiratory muscle training requires active patient participation and effort, exercise motivation and adherence are important determinants of effective implementation. Recent technological developments have enabled the use of mobile application-supported systems and smart adaptors that provide visual feedback during inspiratory muscle training. Visual feedback may improve patient motivation, participation, and usability of the training. However, the acute effects of mobile application-supported inspiratory muscle training with visual feedback have not been adequately investigated in patients undergoing lobectomy after lung cancer surgery.
This study is designed to evaluate the acute effects of conventional inspiratory muscle training and visual feedback-assisted inspiratory muscle training on exercise motivation, dyspnea perception, usability, and patient satisfaction in lung cancer patients undergoing lobectomy via video-assisted thoracic surgery. The study will include clinically stable volunteers aged 18-75 years who are scheduled for lobectomy due to lung cancer and who are able to cooperate with the planned assessments. A total of 40 participants is planned.
Preoperative assessments will be performed on the day before surgery. Demographic and clinical characteristics, including age, height, body weight, smoking history, previous surgeries, and pulmonary function test results, will be recorded. Respiratory muscle strength will be assessed by measuring maximal inspiratory pressure and maximal expiratory pressure using a mouth pressure device.
The intervention will be performed on postoperative day 1 after the patient has been transferred to the ward. First, participants will perform conventional inspiratory muscle training without mobile application support or visual feedback in the morning. After at least two hours of rest, the same inspiratory muscle training protocol will be repeated with a smart adaptor connected to a mobile application, providing visual feedback during the exercise. Inspiratory muscle training will be performed using a threshold-loading device at 40% of maximal inspiratory pressure, with three sets of ten breaths during each session.
After each training session, exercise motivation, dyspnea perception, and patient satisfaction will be evaluated. Exercise motivation will be assessed using the Exercise Motivation Attitude Scale. Dyspnea perception will be assessed using the Modified Borg Scale before and after each intervention. Patient satisfaction, perceived difficulty of training, willingness to continue training, and perceived benefit will be evaluated using 0-10 rating scales. For the mobile application-assisted session, usability will also be assessed using the System Usability Scale. In addition, mobile application-derived data, including the number of successful breaths, total training duration, and total number of breaths, will be recorded.
The primary aim of the study is to determine whether visual feedback-assisted inspiratory muscle training provides more favorable acute effects on exercise motivation and patient adherence compared with conventional inspiratory muscle training. Secondary aims include evaluating dyspnea perception, usability of the mobile application-supported system, patient satisfaction, and objective training data obtained from the smart adaptor. The findings may contribute to the development of technology-supported pulmonary rehabilitation strategies after lobectomy and may guide the integration of visual feedback systems into routine postoperative respiratory physiotherapy.
Studientyp
Einschreibung (Geschätzt)
Phase
- Unzutreffend
Kontakte und Standorte
Studienkontakt
- Name: Funda Alma, MsC
- Telefonnummer: +905079394348
- E-Mail: funda.sirakaya@hacettepe.edu.tr
Studienorte
-
-
Altındağ
-
Ankara, Altındağ, Türkei (türkiye), 06230
- Rekrutierung
- Hacettepe University
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria:
- Volunteering to participate in the study,
- Being clinically stable,
- Being a lung cancer patient scheduled for lobectomy,
- Being between 18 and 75 years of age,
- Being able to cooperate with the tests to be performed.
Exclusion Criteria:
- Presence of any orthopedic or neurological problem that prevents walking,
- History of any surgery involving the thoracic wall,
- Having diseases that may affect respiratory parameters, such as severe heart failure or severe chronic obstructive pulmonary disease (COPD).
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Crossover-Aufgabe
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: Conventional IMT Followed by Visual Feedback-Assisted IMT
Participants randomized to this arm will first receive conventional inspiratory muscle training without visual feedback.
After a rest period of at least two hours, they will receive visual feedback-assisted inspiratory muscle training using a smart adaptor connected to a mobile application.
Both training sessions will be performed using a threshold-loading inspiratory muscle training device at 40% of maximal inspiratory pressure, with three sets of ten breaths.
|
Conventional inspiratory muscle training will be performed without visual feedback or mobile application support.
Training will be delivered using a threshold-loading inspiratory muscle training device at 40% of maximal inspiratory pressure, with three sets of ten breaths.
Visual feedback-assisted inspiratory muscle training will be performed using a threshold-loading inspiratory muscle training device connected to a smart adaptor and mobile application.
The mobile application will provide visual feedback during training.
Training will be performed at 40% of maximal inspiratory pressure, with three sets of ten breaths.
Application-derived data, including the number of successful breaths, total training duration, and total number of breaths, will be recorded.
|
|
Experimental: Visual Feedback-Assisted IMT Followed by Conventional IMT
Participants randomized to this arm will first receive visual feedback-assisted inspiratory muscle training using a smart adaptor connected to a mobile application.
After a rest period of at least two hours, they will receive conventional inspiratory muscle training without visual feedback.
Both training sessions will be performed using a threshold-loading inspiratory muscle training device at 40% of maximal inspiratory pressure, with three sets of ten breaths.
|
Conventional inspiratory muscle training will be performed without visual feedback or mobile application support.
Training will be delivered using a threshold-loading inspiratory muscle training device at 40% of maximal inspiratory pressure, with three sets of ten breaths.
Visual feedback-assisted inspiratory muscle training will be performed using a threshold-loading inspiratory muscle training device connected to a smart adaptor and mobile application.
The mobile application will provide visual feedback during training.
Training will be performed at 40% of maximal inspiratory pressure, with three sets of ten breaths.
Application-derived data, including the number of successful breaths, total training duration, and total number of breaths, will be recorded.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Exercise Motivation
Zeitfenster: Immediately after each intervention on postoperative day 1-2.
|
Exercise motivation will be assessed using the Exercise Motivation Scale after each inspiratory muscle training condition.
The scale includes subdomains related to negative attitudes and thoughts, positive perspective and health, and physical appearance and health.
Higher scores indicate higher exercise motivation.
Scores obtained after conventional inspiratory muscle training and visual feedback-assisted inspiratory muscle training will be compared.
|
Immediately after each intervention on postoperative day 1-2.
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Dyspnea Perception
Zeitfenster: Before and immediately after each intervention on postoperative day 1-2.
|
Dyspnea perception will be assessed using the Modified Borg Scale before and after each inspiratory muscle training condition.
The scale is used to evaluate perceived breathlessness, with higher scores indicating greater dyspnea severity.
Changes in dyspnea perception will be compared between conventional inspiratory muscle training and visual feedback-assisted inspiratory muscle training.
|
Before and immediately after each intervention on postoperative day 1-2.
|
|
System Usability
Zeitfenster: Immediately after each intervention on postoperative day 1-2.
|
The usability of the conventional inspiratory muscle training and visual feedback-assisted inspiratory muscle training system will be assessed using the System Usability Scale after the inspiratory muscle training session.
Higher scores indicate better perceived usability.
|
Immediately after each intervention on postoperative day 1-2.
|
|
Respiratory Muscle Strength
Zeitfenster: Preoperative day, one day before surgery.
|
Respiratory muscle strength will be assessed preoperatively by measuring maximal inspiratory pressure and maximal expiratory pressure using a mouth pressure device.
These measurements will be used to determine the training intensity and to characterize baseline respiratory muscle function.
|
Preoperative day, one day before surgery.
|
|
Patient Satisfaction
Zeitfenster: Immediately after each intervention on postoperative day 1-2.
|
Patient satisfaction with each inspiratory muscle training condition will be evaluated using 0-10 rating scales.
Participants will be asked to rate perceived training difficulty, willingness to continue training, and perceived benefit from the training.
Scores will be compared between conventional inspiratory muscle training and visual feedback-assisted inspiratory muscle training.
|
Immediately after each intervention on postoperative day 1-2.
|
|
Training Performance Data Recorded by the Mobile Application
Zeitfenster: During the visual feedback-assisted intervention on postoperative day 1-2.
|
For the visual feedback-assisted inspiratory muscle training session, application-derived training data will be recorded, including the number of successful breaths, total training duration, and total number of breaths.
|
During the visual feedback-assisted intervention on postoperative day 1-2.
|
Mitarbeiter und Ermittler
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- E-81471704-050-00004500476
- THD-2025-22286 (Andere Zuschuss-/Finanzierungsnummer: Hacettepe University Scientific Research Projects Coordination Unit)
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
Klinische Studien zur Bewegungstraining
-
Klinik für Allgemein- und Viszeralchirurgie, Department...ZurückgezogenLaparoskopie-Training | Roboterchirurgie-TrainingSchweiz
-
Emine Ilkin AydinNoch keine RekrutierungWochenbettpflege | Chatbot-basiertes Training | Webbasiertes Training
-
Ebru TekinAbgeschlossenNeuroathletisches Training | American-Football-Spieler | Reaktives TrainingTürkei (türkiye)
-
Ching-yi WuNational Cheng Kung University Governance Framework for Human Research EthicsAbgeschlossenIntegriertes Dual-Task-Training | Zusätzliches Dual-Task-TrainingTaiwan
-
Acibadem UniversityNoch keine RekrutierungSimulationsbasiertes Training
-
Fenerbahce UniversityAbgeschlossenSimulationsbasiertes TrainingTruthahn
-
University of OxfordAbgeschlossenArthroskopie-TrainingVereinigtes Königreich
-
Taipei Medical UniversityAbgeschlossenChemotherapie-TrainingTaiwan
-
The University of The West IndiesAbgeschlossen
-
ASST Fatebenefratelli SaccoMonash UniversityRekrutierungTraining für KokainkonsumstörungenItalien
Klinische Studien zur Conventional Inspiratory Muscle Training
-
Elif KabasakalRekrutierungBronchiektasen | Funktionelles InspirationsmuskeltrainingTürkei (türkiye)
-
Ondokuz Mayıs UniversityNoch keine RekrutierungPhysiologische Leistung bei gesunden SportlerninnenTürkei (türkiye)
-
Burak KaracaUniversity of GaziantepAbgeschlossen
-
Sahmyook UniversityAbgeschlossenSubakuter Schlaganfall | BilanzdefiziteSüdkorea
-
Hacettepe UniversityRekrutierungPost-COVID-19-Syndrom | Kernstabilisierung | Funktionelles InspirationsmuskeltrainingTürkei (türkiye)
-
Al-Zaytoonah University of JordanAbgeschlossenIntervention bei akutem Schlaganfall | BeatmungspatientenÄgypten
-
Wroclaw University of Health and Sport SciencesRekrutierung
-
National Taiwan Normal UniversityNoch keine RekrutierungIntermittierendes Inspiratory Muscle Training | Eupnea
-
Izmir University of EconomicsAbgeschlossenBelastungsharninkontinenz (SUI)Truthahn
-
FATMA DİLARA AKAR ÇAMYARAbgeschlossen