Literature DB >> 33413658

Impact of a multimedia website with patient experiences of multiple sclerosis (PExMS) on immunotherapy decision-making: study protocol for a pilot randomised controlled trial in a mixed-methods design.

Anna Barabasch1, Karin Riemann-Lorenz2, Christopher Kofahl3,4, Jutta Scheiderbauer4, Desiree Eklund4, Ingo Kleiter5, Jürgen Kasper6, Sascha Köpke7, Susanne Lezius8, Antonia Zapf8, Anne Christin Rahn2,9, Christoph Heesen2,10.   

Abstract

BACKGROUND: A variety of management options (e.g. immunotherapies, lifestyle interventions, and rehabilitation) are available for people with relapsing-remitting multiple sclerosis (RRMS). Besides coping with the diagnosis, people with MS (pwMS) have to make complex decisions such as deciding about immunotherapies. In addition to factual information, reports of patient experiences (PEx) may support patients in decision-making. The added value of PEx in decision-making is not clear, and controlled studies are rare. Therefore, systematic methods are necessary to develop and analyse PEx. As there are no evaluated PEx for MS in Germany, we are currently creating a website presenting PEx structured according to topics and illustrated by video, audio, and text files. We aim to determine the feasibility of an intervention using PEx and evaluate whether PEx may help pwMS in their immunotherapy decision-making processes as a supplement to evidence-based information.
METHODS: This project will follow the Medical Research Council framework for development and evaluation of complex interventions. After the development of a website with PEx, a randomised controlled pilot trial (pilot RCT) will be conducted in 2-3 MS centres, clinics, or rehabilitation centres including 55 pwMS and accompanied by a process evaluation. Patients with a RRMS diagnosis considering immunotherapy are eligible. The primary outcome is decision self-efficacy. Secondary outcomes include preparation for decision-making, decisional conflict, risk knowledge, confidence in active participation, affective forecasting, social support, and self-reported impact of eHealth on its users. Participants will be randomly assigned either to (i) an intervention group with 4 weeks access to an evidence-based patient information resource and the PExMS-website as an adjunct or to (ii) the control group with access to evidence-based information alone. A 6-member advisory panel involving representatives of pwMS, researchers, and neurologists, who accompany the whole project, will mentor this pilot RCT. DISCUSSION: The intervention was developed with systematic methods, created with active patient involvement and in critical appraisal by an expert advisory panel. The study is innovative as it contributes to the controversial evidence on the use of PEx in the context of evidence-based patient information. TRIAL REGISTRATION: ClinicalTrials.gov, NCT04236544.

Entities:  

Keywords:  Decision support; Decision-making; Multiple sclerosis; Narrative information; Patient experiences; Web-based experiential information

Year:  2021        PMID: 33413658      PMCID: PMC7788927          DOI: 10.1186/s40814-020-00749-0

Source DB:  PubMed          Journal:  Pilot Feasibility Stud        ISSN: 2055-5784


  43 in total

1.  Validation of a preparation for decision making scale.

Authors:  Carol Bennett; Ian D Graham; Elizabeth Kristjansson; Stephen A Kearing; Kate F Clay; Annette M O'Connor
Journal:  Patient Educ Couns       Date:  2009-06-26

2.  What should a person with relapsing-remitting multiple sclerosis know? - Focus group and survey data of a risk knowledge questionnaire (RIKNO 2.0).

Authors:  C Heesen; J Pöttgen; A C Rahn; K Liethmann; J Kasper; L Vahter; J Drulovic; A Van Nunen; D Wilkie; Y Beckmann; F Paul; S Köpke; A Giordano; A Solari
Journal:  Mult Scler Relat Disord       Date:  2017-09-21       Impact factor: 4.339

3.  Effect of a decision aid with patient narratives in reducing decisional conflict in choice for surgery among early-stage breast cancer patients: A three-arm randomized controlled trial.

Authors:  Wakako Osaka; Kazuhiro Nakayama
Journal:  Patient Educ Couns       Date:  2016-09-20

Review 4.  Affective forecasting: an unrecognized challenge in making serious health decisions.

Authors:  Jodi Halpern; Robert M Arnold
Journal:  J Gen Intern Med       Date:  2008-07-30       Impact factor: 5.128

5.  The effects of process-focused versus experience-focused narratives in a breast cancer treatment decision task.

Authors:  Victoria A Shaffer; Lukas Hulsey; Brian J Zikmund-Fisher
Journal:  Patient Educ Couns       Date:  2013-08-17

6.  Patient education programme on immunotherapy in multiple sclerosis (PEPIMS): a controlled rater-blinded study.

Authors:  S Köpke; J Kasper; P Flachenecker; H Meißner; A Brandt; B Hauptmann; G Bender; I Backhus; A C Rahn; J Pöttgen; E Vettorazzi; C Heesen
Journal:  Clin Rehabil       Date:  2016-07-10       Impact factor: 3.477

7.  How information about other people's personal experiences can help with healthcare decision-making: a qualitative study.

Authors:  Vikki Ann Entwistle; Emma F France; Sally Wyke; Ruth Jepson; Kate Hunt; Sue Ziebland; Andrew Thompson
Journal:  Patient Educ Couns       Date:  2011-06-08

Review 8.  Health and illness in a connected world: how might sharing experiences on the internet affect people's health?

Authors:  Sue Ziebland; Sally Wyke
Journal:  Milbank Q       Date:  2012-06       Impact factor: 4.911

9.  Validity of the Control Preferences Scale in patients with emotional disorders.

Authors:  Carlos De Las Cuevas; Wenceslao Peñate
Journal:  Patient Prefer Adherence       Date:  2016-11-15       Impact factor: 2.711

10.  Measuring the effects of online health information for patients: item generation for an e-health impact questionnaire.

Authors:  Laura Kelly; Crispin Jenkinson; Sue Ziebland
Journal:  Patient Educ Couns       Date:  2013-04-15
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  5 in total

1.  User Involvement in Myasthenia Gravis Research.

Authors:  Nils Erik Gilhus; Sandra Iren Barkås Hovland
Journal:  Front Neurol       Date:  2022-06-02       Impact factor: 4.086

2.  Experiences of persons with Multiple Sclerosis with lifestyle adjustment-A qualitative interview study.

Authors:  Saskia Elkhalii-Wilhelm; Anna Sippel; Karin Riemann-Lorenz; Christopher Kofahl; Jutta Scheiderbauer; Sigrid Arnade; Ingo Kleiter; Stephan Schmidt; Christoph Heesen
Journal:  PLoS One       Date:  2022-05-27       Impact factor: 3.752

3.  Experiences of persons with multiple sclerosis with rehabilitation-a qualitative interview study.

Authors:  Donya Ghaidar; Anna Sippel; Karin Riemann-Lorenz; Christopher Kofahl; Rebecca Morrison; Ingo Kleiter; Stephan Schmidt; Christian Dettmers; Holger Schulz; Christoph Heesen
Journal:  BMC Health Serv Res       Date:  2022-06-11       Impact factor: 2.908

4.  Development and evaluation of a website with patients experiences of multiple sclerosis: a mixed methods study.

Authors:  Anna Sippel; Jutta Scheiderbauer; Désirée Eklund; Sigrid Arnade; Stephan Schmidt; Ingo Kleiter; Rebecca Morrison; Christopher Kofahl; Christoph Heesen
Journal:  BMC Neurol       Date:  2022-04-20       Impact factor: 2.903

5.  Validation of the German eHealth impact questionnaire for online health information users affected by multiple sclerosis.

Authors:  Anna Sippel; Karin Riemann-Lorenz; Jana Pöttgen; Renate Wiedemann; Karin Drixler; Eva Maria Bitzer; Christine Holmberg; Susanne Lezius; Christoph Heesen
Journal:  BMC Med Inform Decis Mak       Date:  2022-08-16       Impact factor: 3.298

  5 in total

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