Rapid Instructed Task Learning is impaired after stroke and associated with impairments in prepotent inhibition and processing speed.

Abstract

Background: Motor rehabilitation is a central contributor to motor recovery after stroke. This process could be hampered by stroke-associated cognitive impairments, such as the capability to rapidly follow instructions (Rapid instructed task learning, RITL). RITL was never directly studied in old adults and subjects with stroke. The aim of this study was to assess RITL following stroke and its underlying cognitive determinants. Methods: 31 subjects with chronic stroke and 36 age-matched controls completed a computerized cognitive examination that included an anti-saccade task for measuring prepotent inhibition and processing speed and stimulus-response association task (NEXT) for measuring RITL and proactive inhibition. Results: RITL abilities were impaired after stroke, together with prepotent inhibition and processing speed. A correlation analysis revealed that RITL is associated with prepotent inhibition abilities and with processing speed. Conclusions: Subjects with stroke show impairments in the ability to follow instructions, that may be related to their impaired prepotent inhibition and processing speed. The causal effect of RITL impairments on the responsivity to rehabilitation and on motor recovery should be examined.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This work was supported by the Israeli Science Foundation grant 1244/22 to LS

Author Declarations

I 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:

The study was approved by the Ben-Gurion institutional Helsinki committee (for control subjects) and by the Regional Ethical Review Board at Sheba Medical Center, Israel (Approval Number 6218-19-SMC) (for stroke subjects)

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the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 Availability

All data produced in the present study are available upon reasonable request to the authors

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