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Table 1 Major endpoints

From: Assessing the effect of an evidence-based patient online educational tool for people with multiple sclerosis called UMIMS—understanding magnetic resonance imaging in multiple sclerosis: study protocol for a double-blind, randomized controlled trial

Instrument

Measurement time point

Enrollment

Allocation

Post-allocation

t−1

t0

t1

t2

t3

Eligibility screen

x

   

s

Informed consent

x

    

Allocation

x

    

Sociodemographic data

x

x

   

PDDS

 

x

   

MS-related data and resource use

 

x

   

MRI-RIKNO

 

xa

x

  

Subjective knowledge

 

x

x

  

MRI-EMA

 

x

x

x

 

CPS

 

x

x

x

 

Numeracy

 

x

   

Threat by MS

 

x

x

  

HADS

 

x

x

  

Process evaluation

  

x

x (patient and physician)

x

MAPPIN’SDM

   

x (patient and physician)

 

MAPPIN’SDM audio (n = 5 CG/IG)

   

x (external rater)

 

Treatment/MRI decision

   

x

x

  1. t1 2 weeks after allocation and access to the intervention/control website, t2 immediately after patient-physician encounter, t3 6 months after patient-physician encounter, CG control group, CPS Control Preference Scale, HADS Hospital Anxiety and Depression Scale, IG intervention group, MAPPIN’SDM Multifocal Approach to Sharing in Shared Decision Making, MRI-EMA magnetic resonance imaging-emotions and attitude questionnaire, MRI-RIKNO magnetic resonance imaging-risk knowledge questionnaire, PDDS patient-determined disease steps
  2. aPrimary endpoint