Cognitive impairment is highly prevalent in people with progressive multiple sclerosis. Computerized cognitive training techniques have demonstrated some success at targeting core cognitive processes but are criticized for lack of transfer to real-world tasks. Research in physical rehabilitation has demonstrated the efficacy of high volume, moderate intensity task-specific training (TST) that is monitored, progressed and ideally practiced in real-world environments to enhance learning, transferability and support neurorecovery of motor functions. Findings demonstrate that TST influences activity and participation outcomes, leads to improved cortical reorganization, and focuses on activities that align with a persons daily life and specific goals. Our MSCanRehab group adapted the same principles to develop a novel comprehensive interdisciplinary approach to cognitive rehabilitation that combines core cognitive process training (CCPT), TST and a modified Cognitive Orientation to Daily Occupational Performance (CO-OP) approach. The cognitive TST was individualized to participant goals identified using the Canadian Occupational Performance Measure and further tailored based on their areas of cognitive weakness. A modified CO-OP process was utilized that incorporated CCPT and cognitive TST personalized to meet meaningful participant goals and improve occupational performance. Cognitive TST utilized goal-directed practice and repetition focused on cognitive skills (vs. impairments) using real-world tasks. Task complexity and challenge was gradually increased and progressively adapted with emphasis on active participation and problem solving. A case example demonstrates how the intervention was implemented. Components of the intervention are described using the TIDieR-Rehab checklist to ensure a comprehensive description, with emphasis on essential elements and dosage parameters.
Competing Interest StatementThe authors have declared no competing interest.
Clinical TrialThis was a feasibility study and was not registered in a trial registry.
Funding StatementThis study was funded by the International Progressive MS Alliance.
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
Ethics approval was received from the University of Ottawa Research Ethics Board.
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
Yes
I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
Data AvailabilityAll data produced in the present study are available upon reasonable request to the authors.
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