Multiple Sclerosis (MS) Clinical Trial
— SMARTCAREOfficial title:
Neurostatus-SMARTCARE in Comparison to Standard Neurostatus- EDSS® - a Swiss Multicenter Randomized Cross-over Study
Verified date | March 2024 |
Source | University Hospital, Basel, Switzerland |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The Expanded Disability Status Scale (EDSS) is the gold-standard in assessing disability in Multiple Sclerosis (MS). Its current digital form, the Neurostatus-eEDSS®, often serves as primary endpoint in MS clinical trials. The pandemic revealed the need for telemedical alternatives to the in-clinic assessment. Therefore, Neurostatus-SMARTCARE was developed: A trained and certified non-neurologist Health Care Professional (HCP) examines the patient while the examination is being video-recorded. The stored video allows a neurologist to re-assess the examination at a later point of time. The future application could be in-home visits through HCPs, in decentralized clinical trials as well as in routine care. In this study, the concordance rate of Neurostatus examinations between neurologists and HCPs is investigated. With a concordance rate significantly higher than 80%, Neurostatus-SMARTCARE by HCPs can be considered equal to the standard Neurostatus-EDSS by neurologists.
Status | Completed |
Enrollment | 101 |
Est. completion date | March 1, 2024 |
Est. primary completion date | November 17, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - 18 years old at the time of signing the informed consent - Clinically definite MS, confirmed through the medical chart - At least one documented EDSS assessment within two (2) years prior to inclusion - The participant must be capable of giving signed informed consent Exclusion Criteria: - Insufficient knowledge of the German language, i.e. inability to understand the patient information or to follow the instructions and questions during the EDSS assessment |
Country | Name | City | State |
---|---|---|---|
Switzerland | Neurologic Clinic and Policlinic, University Hospital Basel | Basel | |
Switzerland | Luzerner Kantonsspital | Luzern 16 |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Basel, Switzerland | Novartis Pharma AG, Basel, Switzerland |
Switzerland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Inter-rater reliability, i.e. the concordance rate between Neurostatus-SMARTCARE and Neurostatus-EDSS® at EDSS step level | The pairwise concordance among all EDSS-steps between a neurologist's and a nurse's assessment of the the same participant at one visit will be tested and an overall concordance rate of all EDSS-steps.
The true concordance level needs to be at least 89% to have a reasonable chance of demonstrating that the observed rate is significantly higher than 80%. If this can be shown, it can be concluded that Neurostatus-SMARTCARE is equivalent to the standardized Neurostatus-EDSS in clinical routine or clinical trials. This would allow HCPs to assess the Neurostatus-EDSS with the same quality as neurologists. |
1.5 - 2 hours per study visit for each participant | |
Secondary | Inter-rater reliability at subscore level between Neurostatus-SMARTCARE and standard Neurostatus-EDSS® | The pairwise concordance among all subscores between a neurologist's and a nurse's assessment of the the same participant at one visit will be tested and an overall concordance rate of all subscores. | 1.5 - 2 hours per study visit for each participant | |
Secondary | Inter-rater reliability at Functional System Score (FSS) levels between Neurostatus-SMARTCARE and standard Neurostatus-EDSS® | The pairwise concordance among all FSS between a neurologist's and a nurse's assessment of the the same participant at one visit will be tested and an overall concordance rate of all FSS. | 1.5 - 2 hours per study visit for each participant | |
Secondary | Number of assessments rated correctly by neurologists in comparison to HCPs | When discrepancies occur between neurologists and nurses at EDSS step level, it will be calculated how often the neurologists had assessed the correct result and how often the nurses. | Through study completion, an average of 1.5 years | |
Secondary | Number and type of the same error occurring more than once at the individual rater level | It will be tested if raters make the same error more than once, i.e. if they make typical errors that could be corrected through re-training. Therefore the number of "more-than-once-errors" will be collected and the type of error, e.g. errors through a false examination technique or a calculation error in determining the FSS/ EDSS step. | Through study completion, an average of 1.5 years | |
Secondary | Inter-rater reliability in capturing the number of changes in the Expanded Disability Status Scale (EDSS) through worsening and progression or improvement occurring between the first and second measurement. | I twill be tested if neurologists and nurses detect EDSS changes after 6 months equally, i.e. if they assign the same changed EDSS step.
Note: Changes in the EDSS are defined in steps of 0.5 points. Increasing numbers of the EDSS step mean worsening, decreasing numbers mean improvement. An increase of 1.0 point over 3 months is usually considered MS progression. |
Through study completion, an average of 1.5 years |
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