| |  Online-Ressource |
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| Verfasst von: | Ueter, Sophie [VerfasserIn]  |
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| | Taebi, Niki [VerfasserIn] |
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| | Weiß, Christel [VerfasserIn] |
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| | Hetjens, Michael [VerfasserIn] |
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| | Reißfelder, Christoph [VerfasserIn] |
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| | Blank, Susanne [VerfasserIn] |
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| | Otto, Mirko [VerfasserIn] |
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| | Yang, Cui [VerfasserIn] |
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| Titel: | Study protocol for a non-inferiority, multicenter, randomized study to evaluate a smartphone app-based follow-up program after bariatric surgery (BELLA plus trial) |
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| Verf.angabe: | Sophie Ueter, Niki Taebi, Christel Weiß, Michael Hetjens, Christoph Reissfelder, Susanne Blank, Mirko Otto, Cui Yang |
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| E-Jahr: | 2024 |
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| Jahr: | September 2024 |
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| Umfang: | 7 S. |
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| Illustrationen: | Illustrationen |
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| Fussnoten: | Online verfügbar: 27. Juni 2024, Artikelversion: 5. Juli 2024 ; Gesehen am 22.10.2024 |
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| Titel Quelle: | Enthalten in: Contemporary clinical trials |
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| Ort Quelle: | Amsterdam [u.a.] : Elsevier Science, 2005 |
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| Jahr Quelle: | 2024 |
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| Band/Heft Quelle: | 144(2024), Artikel-ID 107615$m9, Seite 1-7 |
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| ISSN Quelle: | 1559-2030 |
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| Abstract: | Introduction - Adherence to follow-up (FU) care after bariatric surgery is poor despite strong recommendations. In our pilot Bella trial, we demonstrated that a completely remote follow-up program via smartphone is feasible and safe for patients after bariatric surgery. Building on this, we aim to verify our results in a multicenter, randomized controlled setting. - Methods - This trial plans to enroll 410 participants undergoing primary bariatric surgery in seven German bariatric centers. Participants are randomized into two groups: a control group receiving in-person FU according to the standard in the bariatric centers, and an interventional group monitored using a smartphone application (app). The app sends standardized questionnaires and reminders regarding regular vitamin intake and exercises. The built-in messaging function enables patients to communicate remotely with medical care professionals. After one year, all participants are evaluated at their primary bariatric centers. The primary outcome is weight loss 12 months after surgery. The secondary outcomes include obesity-related comorbidities, quality of life, serum values of vitamins and minerals, body impedance analysis, visits to the emergency department or readmission, patient compliance, and medical staff workload. - Discussion - The current study is the first prospective, individually randomized-controlled, multicenter trial where a mobile application completely replaces traditional in-person visits for post-bariatric surgery follow-ups in bariatric centers. |
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| DOI: | doi:10.1016/j.cct.2024.107615 |
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| URL: | Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.
kostenfrei: Volltext: https://doi.org/10.1016/j.cct.2024.107615 |
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| | kostenfrei: Volltext: https://www.sciencedirect.com/science/article/pii/S1551714424001988 |
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| | DOI: https://doi.org/10.1016/j.cct.2024.107615 |
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| Datenträger: | Online-Ressource |
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| Sprache: | eng |
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| Sach-SW: | mHealth |
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| | Obesity |
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| | Patient adherence |
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| | Remote monitoring |
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| | Telemedicine |
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| | Weight loss surgery |
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| K10plus-PPN: | 1906379424 |
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| Verknüpfungen: | → Zeitschrift |
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Study protocol for a non-inferiority, multicenter, randomized study to evaluate a smartphone app-based follow-up program after bariatric surgery (BELLA plus trial) / Ueter, Sophie [VerfasserIn]; September 2024 (Online-Ressource)
