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| ID | Type | Description | Link |
|---|---|---|---|
| THD-2025-22286 | Other Grant/Funding Number | Hacettepe University Scientific Research Projects Coordination Unit |
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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.
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Conventional IMT Followed by Visual Feedback-Assisted IMT | Experimental | 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. |
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| Visual Feedback-Assisted IMT Followed by Conventional IMT | Experimental | 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. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Conventional Inspiratory Muscle Training | Other | 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. |
| Measure | Description | Time Frame |
|---|---|---|
| Exercise Motivation | 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. |
| Measure | Description | Time Frame |
|---|---|---|
| Dyspnea Perception | 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. This scale ranges from 0 to 10, where 0 indicates no dyspnea and 10 indicates maximal or very severe dyspnea. Changes in dyspnea perception will be compared between conventional inspiratory muscle training and visual feedback-assisted inspiratory muscle training. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Funda Alma, MsC | Contact | +905079394348 | funda.sirakaya@hacettepe.edu.tr |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hacettepe University | Recruiting | Ankara | Altındağ | 06230 | Turkey (Türkiye) |
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Participants will receive both conventional inspiratory muscle training and visual feedback-assisted inspiratory muscle training in a randomized crossover design. The order of the two interventions will be randomized, with at least two hours of rest between sessions.
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| Visual Feedback-Assisted Inspiratory Muscle Training | Other | 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. |
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| Before and immediately after each intervention on postoperative day 1-2. |
| System Usability | 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. The System Usability Scale is a 10-item questionnaire scored from 0 to 100, where 0 indicates the lowest perceived usability and 100 indicates the highest perceived usability. Higher scores indicate a better outcome, reflecting greater perceived usability of the system. | Immediately after each intervention on postoperative day 1-2. |
| Respiratory Muscle Strength | 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 | 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. |
| The number of successful breaths Recorded by the Mobile Application | For the visual feedback-assisted inspiratory muscle training session, application-derived training data will be recorded, as the number of successful breaths. | During the visual feedback-assisted intervention on postoperative day 1-2. |
| Total training duration Recorded by the Mobile Application | For the visual feedback-assisted inspiratory muscle training session, application-derived training data will be recorded, as the total training duration. | During the visual feedback-assisted intervention on postoperative day 1-2. |
| Total number of breaths Recorded by the Mobile Application | For the visual feedback-assisted inspiratory muscle training session, application-derived training data will be recorded, as total number of breaths. | During the visual feedback-assisted intervention on postoperative day 1-2. |
| ID | Term |
|---|---|
| D008175 | Lung Neoplasms |
| D002289 | Carcinoma, Non-Small-Cell Lung |
| ID | Term |
|---|---|
| D012142 | Respiratory Tract Neoplasms |
| D013899 | Thoracic Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D002283 | Carcinoma, Bronchogenic |
| D001984 | Bronchial Neoplasms |
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