Skip to content

Benefit and risk information for medications in multiple sclerosis

Improving understanding and recall of risk information relating to multiple sclerosis medication - developing an evidence-based clinical tool for assisting communication and understanding of multiple sclerosis medication risk information between patients and health professionals

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN17318966
Enrollment
24
Registered
2016-10-26
Start date
2016-10-28
Completion date
Unknown
Last updated
2021-02-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple sclerosis Nervous System Diseases Multiple sclerosis

Interventions

The intervention in the study is the evidence-based protocol. This protocol will be used to provide information about medication risks and benefits from findings in the literature, and the observation

Sponsors

Royal Holloway, University of London
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Diagnosis of relapsing-remitting multiple sclerosis (RRMS) by a consultant neurologist to best current criteria (i.e. not clinically isolated syndrome (CIS), likely Polman et al., 2011) 2. Able and willing to give informed consent 3. Able to meet tasks demands of study in terms of sensorimotor abilities 4. Ages 18 to 60

Exclusion criteria

Exclusion criteria: 1. Significant change in medication in last 4 weeks 2. Relapse recovery within last 4 weeks 3. Significant psychiatric history/condition 4. Significant medical condition (other than MS), personal or social circumstances likely to influence study participation

Design outcomes

Primary

MeasureTime frame
Patients' decisional conflict, assessed using the Decisional Conflict Scale directly after each condition (i.e. four times in total)

Secondary

MeasureTime frame
Patients' understanding of the information provided during the study, assessed using an author-designed questionnaire directly after each condition (i.e. four times in total)

Countries

United Kingdom

Contacts

Public ContactGurpreet Reen
Gurpreet.reen.2014@live.rhul.ac.uk+44 (0)787 845 1844

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 24, 2026