M. Gugatschka, N. Egger, R. Rehb, C. Reiter, M. Rudes, R. Mischak, K. Haspl
{"title":"Development of an e-Health Software for Speech and Swallowing Rehabilitation Following Laryngectomy","authors":"M. Gugatschka, N. Egger, R. Rehb, C. Reiter, M. Rudes, R. Mischak, K. Haspl","doi":"10.1002/lio2.70136","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Objectives</h3>\n \n <p>We present data from a feasibility study where patients following laryngectomy and/or hemi-laryngectomy received speech and swallowing rehabilitation via a newly designed e-health software.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Patients were recruited during their stay at the hospital and were equipped with a tablet upon discharge. Alternatively, patients who already underwent training but did not improve significantly were included to receive a more intense training. The training protocol comprised asynchronous (e.g., self-assessment and pre-defining training protocols) and synchronous (e.g., video communication) therapies; participation lasted for 8 weeks. General demographic parameters, as well as specific parameters (quality of life, speech comprehensibility) were assessed pre- and post-interventional.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Our cohort consisted of eight patients (mean age: 69 years.) Essential outcome parameters improved significantly (weight, comprehensibility for syllables).</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>Our feasibility study showed that our software is safe and easy-to-use and can be easily integrated into patients' everyday lives. Key parameters such as weight and comprehensibility improved after just 8 weeks of training.</p>\n </section>\n \n <section>\n \n <h3> Level of Evidence</h3>\n \n <p>NA</p>\n </section>\n </div>","PeriodicalId":48529,"journal":{"name":"Laryngoscope Investigative Otolaryngology","volume":"10 2","pages":""},"PeriodicalIF":1.6000,"publicationDate":"2025-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/lio2.70136","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Laryngoscope Investigative Otolaryngology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/lio2.70136","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OTORHINOLARYNGOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives
We present data from a feasibility study where patients following laryngectomy and/or hemi-laryngectomy received speech and swallowing rehabilitation via a newly designed e-health software.
Methods
Patients were recruited during their stay at the hospital and were equipped with a tablet upon discharge. Alternatively, patients who already underwent training but did not improve significantly were included to receive a more intense training. The training protocol comprised asynchronous (e.g., self-assessment and pre-defining training protocols) and synchronous (e.g., video communication) therapies; participation lasted for 8 weeks. General demographic parameters, as well as specific parameters (quality of life, speech comprehensibility) were assessed pre- and post-interventional.
Results
Our cohort consisted of eight patients (mean age: 69 years.) Essential outcome parameters improved significantly (weight, comprehensibility for syllables).
Conclusion
Our feasibility study showed that our software is safe and easy-to-use and can be easily integrated into patients' everyday lives. Key parameters such as weight and comprehensibility improved after just 8 weeks of training.