UMIMS: Understanding Magnetic Resonance Imaging in Multiple Sclerosis

Sponsor
Universitätsklinikum Hamburg-Eppendorf (Other)
Overall Status
Recruiting
CT.gov ID
NCT03872583
Collaborator
Sanofi (Industry)
120
1
2
39.6
3

Study Details

Study Description

Brief Summary

Magnetic resonance imaging (MRI) results play a major role in the lives of people with multiple sclerosis (pwMS). Even though MRI is used for diagnosis, prognosis and therapy control, pwMS' knowledge concerning this complex matter is scarce. Without adequate disease-specific knowledge, pwMS cannot truly make an informed choice when considering their MRI results (e.g. necessity of future MRI scans or therapy change).

The investigators have developed an innovative, evidence-based and interactive online education tool called "Understanding MRI in MS", which incorporates all relevant information about MRI in MS and its implications in disease management.

In this randomized, controlled and double-blind trial the tool's effect on MRI-specific knowledge, self-perceived competence and involvement in medical decision, that are based on MRI results will be assessed.

Condition or Disease Intervention/Treatment Phase
  • Other: Understanding MRI in MS (website)
  • Other: Control website
N/A

Detailed Description

For the randomized controlled trial (RCT), n=120 consecutive patients of 4 centers, for whom a brain (or brain and spine) MRI scan is planned within the next 6 months, will be invited to participate in the trial. Eligible patients will be asked to participate, and, if willing, will receive information about the study by the recruiting physician and written consent will be obtained. Participants will then answer a baseline questionnaire including demographic data, numeracy, attitude and emotions towards MRI (MRI-emotions and attitude questionnaire, MRI-EMA, newly developed) and MRI-specific knowledge (MRI-risk knowledge questionnaire 2.0, MRI-RIKNO 2.0, newly developed).

Patients will then be randomized into two groups: The intervention group of n=60 participants gets access to the web-based educational tool, the control group of n=60 to a sham intervention with standard information on MRI.

Participants will be asked to provide an e-mail address via which the login for the educational tool will be delivered. After two weeks participants will be asked to fill out the following tools:

Primary endpoint

  • MRI-risk knowledge questionnaire 2.0 (MRI-RIKNO 2.0) (newly developed)

  • MRI-emotions and attitude questionnaire (MRI-EMA) (newly developed)

  • Threat by MS

  • Autonomy preferences (Control Preference Scale)

  • Subjective knowledge (VAS scale) (22)

Within the course of 2 weeks to 6 months the scheduled MRI will take place, followed by a patient-physician encounter, in which the MRI results are discussed. Directly after this encounter patients and physicians will be asked to answer MAPPIN'SDM questionnaires to assess perceived shared decision making behaviour and realization of autonomy preferences (Control reference scale). All patients will also be asked questions concerning any decisions taken based on the MRI, either a start/change of treatment or agreement on a new MRI in a defined time-frame. N=5 patients of each arm in the study center in Hamburg will be randomly selected and the communication of results during this consultation will be audiotaped and evaluated using the MAPPIN'SDM observer rating approach.

In a telephone follow-up after 6 months, implementation of the decisions will be checked.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
120 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Randomized, controlled, double-blind trialRandomized, controlled, double-blind trial
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Masking Description:
Participants, physicians, outcome assessors and investigator will be blinded.
Primary Purpose:
Other
Official Title:
Understanding Magnetic Resonance Imaging in Multiple Sclerosis - a Randomized, Controlled, Double Blind Trial
Actual Study Start Date :
Mar 15, 2019
Anticipated Primary Completion Date :
Jul 1, 2021
Anticipated Study Completion Date :
Jul 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Understanding MRI in MS (website)

Participants will receive access to a newly developed, innovative, interactive and evidence-based education tool about magnetic resonance imaging in multiple sclerosis.

Other: Understanding MRI in MS (website)
Access to an innovative, interactive and evidence-based online education tool about MRI in multiple sclerosis.

Active Comparator: Control website

Participants will receive access to a specifically designed control website containing the information about magnetic resonance imaging in multiple sclerosis, that is freely available on the websites of major European multiple sclerosis self help organization (Australia, Belgium, Canada, France, Germany, Great Britain, Netherland, USA).

Other: Control website
Access to a specifically designed control website containing information on MRI in MS freely available on the websites of major European MS self-help organizations.

Outcome Measures

Primary Outcome Measures

  1. Magnetic resonance imaging risk knowledge questionnaire 2.0 (MRI-RIKNO 2.0) [2 weeks]

    15-item magnetic resonance imaging-specific knowledge questionnaire (min. points 0, maximum points 22; higher values indicate greater knowledge)

Secondary Outcome Measures

  1. Emotions and attitude towards magnetic resonance imaging (MRI-EMA) [Baseline, 2 weeks]

    Validated 10-item questionnaire on emotions and attitude towards magnetic resonance imaging, sub-scales (min. value: 1, max. value: 4; higher values indicate greater expression of the feature): 1) Fear of MRI scan, 2) Fear of MRI results, 3) Feeling of control, 4) Feeling of competence

  2. Control preference scale (CPS) [Baseline, 2 weeks, after patient-physician encounter (i.e. 4 weeks to 6 months after baseline)]

    Scale to assess autonomy preferences during medical decisions (5 categories between complete autonomy and paternalistic decision making as the extremes)

  3. Threat by MS [baseline, 2 weeks]

    Visual analogue scale to assess anxiety associated with disease progression (min. 0, max. 100; higher values indicate higher subjective threat)

  4. Hospital Anxiety and Depression Scale (HADS) [Baseline, 2 weeks]

    Questionnaire to assess anxiety and depression (min. 0, max. 42 points (21 points for each subscale, subscales are added); higher values indicate more severe depression/anxiety)

  5. Multifocal Approach to Sharing in Shared Decision Making (MAPPIN'SDM) [after patient-physician-encounter (i.e. 4 weeks to 6 months after baseline)]

    Tool to assess the amount of shared decision making during a patient-physician encounter (min. value 0, max. value 45; higher values indicated higher level of shared decision making)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 18 years 65 years

  • MRI within 6 weeks to 6 months

  • internet access AND

  • diagnosis of relapsing-remitting MS (RRMS) according to the McDonald criteria (Thompson et al., 2018), <10 years disease duration + active disease course (i.e. therapy change or new T2 lesion within the previous year) OR

  • clinically isolated syndrome (CIS) (with at least one MS-typical T2 lesion)

Exclusion Criteria:
  • diagnosis of secondary-progressive MS

  • diagnosis of primary-progressive MS

  • diagnosis or suspected central nervous system disease other than MS

  • severe cognitive deficit

  • major psychiatric illness

  • patients who are related to medical personnel

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Medical Centre Hamburg-Eppendorf Hamburg Germany 20246

Sponsors and Collaborators

  • Universitätsklinikum Hamburg-Eppendorf
  • Sanofi

Investigators

  • Principal Investigator: Christoph Heesen, Prof., University Medical Center Hamburg-Eppendorf; Institute for Neuroimmunology and Multiple Sclerosis

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Universitätsklinikum Hamburg-Eppendorf
ClinicalTrials.gov Identifier:
NCT03872583
Other Study ID Numbers:
  • PV5722
First Posted:
Mar 13, 2019
Last Update Posted:
Feb 2, 2021
Last Verified:
Jan 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Universitätsklinikum Hamburg-Eppendorf
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 2, 2021