Development, piloting, and evaluation of an evidence-based informed consent form for total knee arthroplasty (EvAb-Pilot): a protocol for a mixed methods study
| Autor: | Anke Steckelberg, Sandro Zacher, Stefanie Bühn, Henning Rosenau, Felicia Steffen, Julia Lauberger, Tim Mathes, Andreas Böhmer, Alina Weise, Julia Lühnen, Deha Murat Ates |
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| Jazyk: | angličtina |
| Rok vydání: | 2021 |
| Předmět: |
Informed consent form
Medicine (General) Mixed methods Evidence-based practice Medicine (miscellaneous) Anxiety Risk communication Total knee arthroplasty (TKA) Study Protocol R5-920 Informed consent Intervention (counseling) Medicine Protocol (science) business.industry Liability Nocebo effect Pilot medicine.disease Clinical trial Nocebo Effect Medical emergency medicine.symptom business Evidence-based health information |
| Zdroj: | Pilot and Feasibility Studies, Vol 7, Iss 1, Pp 1-11 (2021) Pilot and Feasibility Studies |
| ISSN: | 2055-5784 |
| Popis: | Background Practitioners frequently use informed consent forms to support the physician-patient communication and the informed consent process. Informed consent for surgery often focuses on risk centered information due to high liability risks for treatment errors. This may affect patients’ anxiety of adverse events and the nocebo effect. This study focuses on the optimization of pre-surgical information on risks and complications, and at the same time reconciles these information with legal requirements. Methods The development, piloting, and evaluation of evidence-based informed consent forms for total knee arthroplasty (TKA) and related anesthesia procedures will follow the UK MRC Framework for developing and evaluating complex interventions. Conducting different sub-studies, we will (I) qualitatively explore the information acquisition and decision-making processes, (II) develop and pilot test evidence-based informed consent forms on the example of TKA and related anesthesia procedures, (III) conduct a monocentric interrupted time series (ITS) pilot study to evaluate the effects of evidence-based informed consent forms in comparison with standard consent forms, and (IV) perform a process evaluation to identify barriers and facilitators to the implementation of the intervention and to analyze mechanisms of impact. Discussion The evidence-based and understandable presentation of risks in informed consent forms aims at avoiding distorted risk depiction and strengthening the patients’ competencies to correctly assess the risks of undergoing surgery. This might reduce negative expectations and anxiety of adverse events, which in turn might reduce the nocebo effect. At the same time, the practitioners’ acceptance of evidence-based informed consent forms meeting legal requirements could be increased. Trial registration ClinicalTrials.gov, NCT04669483. Registered 15 December 2020. German Clinical Trials Registry, DRKS00022571. Registered 15 December 2020 |
| Databáze: | OpenAIRE |
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