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Acute Effects of Visual Feedback-Assisted Inspiratory Muscle Training After Lobectomy

9 de junio de 2026 actualizado por: Funda Sirakaya, Hacettepe University

Evaluation of the Acute Effects of Respiratory Muscle Strength Training With Visual Feedback in Lung Cancer Patients Undergoing Lobectomy

This study aims to evaluate the acute effects of inspiratory muscle training performed with and without a mobile application providing visual feedback on exercise motivation, patient adherence, dyspnea perception, usability, and patient satisfaction in lung cancer patients undergoing lobectomy via video-assisted thoracic surgery. Participants will perform conventional inspiratory muscle training without visual feedback in the morning on postoperative day 1 after transfer to the ward. After at least two hours of rest, the same exercise protocol will be repeated with a smart adaptor connected to a mobile application to provide visual feedback. Inspiratory muscle training will be performed using a threshold-loading device at 40% of maximal inspiratory pressure, with three sets of ten breaths. Outcomes will be assessed before and/or after each session as appropriate.

Descripción general del estudio

Descripción detallada

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.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

40

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

    • Altındağ
      • Ankara, Altındağ, Turquía (Türkiye), 06230
        • Reclutamiento
        • Hacettepe University

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

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).

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación cruzada
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
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.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Exercise Motivation
Periodo de tiempo: 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.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Dyspnea Perception
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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.

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

1 de diciembre de 2025

Finalización primaria (Estimado)

1 de diciembre de 2026

Finalización del estudio (Estimado)

1 de marzo de 2027

Fechas de registro del estudio

Enviado por primera vez

9 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

9 de junio de 2026

Publicado por primera vez (Actual)

12 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

12 de junio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

9 de junio de 2026

Última verificación

1 de junio de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • E-81471704-050-00004500476
  • THD-2025-22286 (Otro número de subvención/financiamiento: Hacettepe University Scientific Research Projects Coordination Unit)

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

INDECISO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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