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Tests two telecare programs for cognitive problems after minor stroke

Tests telecare psychoeducation and computerized cognitive stimulation in adults with minor stroke.

Plain-language title generated from the registry record
Registry title: Early-phase Telecare Programs for Minor Stroke

Key facts

Where
Bordeaux, Lille, and Saint-Genis-Laval, FranceSee the 3 sites

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 65 years old?

Source: NCT06306144, who can take part

Where in France

  • CHU de BordeauxBordeaux, FranceNo longer taking part
  • CHU LilleLille, FranceNo longer taking part
  • Hôpital Henry GabrielleSaint-Genis-Laval, FranceNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Hospices Civils de Lyon
Trial code
NCT06306144
Record updated
18 April 2025
Original description
Minor strokes (few acute neurological symptoms ; NIHSS score <5), represent almost 65% of cerebrovascular ischemic events. The increasing incidence of stroke in people under 65, together with advances in diagnostic and revascularization techniques, mean that post-stroke life expectancy is now in the order of decades. Most patients with minor stroke are rapidly discharged from hospital, with follow-up focused on secondary prevention and they are offered little or no rehabilitation.Read full original descriptionShow less

Mild Cognitive Impairment After Minor Stroke: Evaluation of Early-phase Telecare Programs (Psychoeducation and Computerized Cognitive Stimulation)

Minor strokes (few acute neurological symptoms ; NIHSS score <5), represent almost 65% of cerebrovascular ischemic events. The increasing incidence of stroke in people under 65, together with advances in diagnostic and revascularization techniques, mean that post-stroke life expectancy is now in the order of decades. Most patients with minor stroke are rapidly discharged from hospital, with follow-up focused on secondary prevention and they are offered little or no rehabilitation.

However, up to 70% of patients with minor stroke experience difficulties resuming their social or professional activities, which can lead to social and economic disruption (delayed/compromised return to work) and an increased risk of depression. While some care recommendations exist for this population, in France there is no consensus nor identified care pathway for follow-up assessment or management of these patients. Furthermore, existing services are unevenly distributed across the country, and research into the effectiveness of rehabilitation is still scarce, leading to uncertainty as to which interventions should be prioritized to decrease difficulties related to cognitive impairment.

Since there are currently no rehabilitation proposals in France for patients with mild cognitive impairment after mild stroke, in this trial the investigaror will investigate the effectiveness of two six-week telerehabilitation programs each consisting of a weekly session supervised by a therapist and a self-rehabilitation session. The aim of this multicenter randomized controlled trial is the evaluate the relevance and feasibility of early identification of patients eligible for a cognition-focused management proposal and the efficacy of two telecare programs, (a) psychoeducation and (b) computerized cognitive rehabilitation.

Inclusion: Man or woman, aged between 18 and 65 years old; Hospitalization for a first stroke; Minor stroke: NIHSS score < 5 on discharge from neurovascular unit; Post-stroke delay < 8 weeks; Living at home (not institutionalized); Affiliated with social security or benefiting from such a scheme; French language; Presence of a cognitive complaint (FACT-Cog "perceived cognitive impairments" subscale score < 55) and absence of major cognitive impairment; Signature of informed consent.

Exclusion: History of stroke; Uncorrected hearing or visual impairment; Neurological pathology other than stroke or disabling psychiatric disorder; Unstabilized epilepsy; Undergoing cognitive rehabilitation in another context or having integrated a post-stroke therapeutic education program; Living in a white zone that does not allow for remote rehabilitation; Unable to connect to the Internet; Pregnant, parturient or breast-feeding women* (interview data); Persons deprived of their liberty by judicial or administrative decision; Persons admitted to a health or social institution for purposes other than research; Adults under legal protection (guardianship, curatorship); Taking part in other interventional research involving a period of exclusion still in progress at pre-inclusion.

ClinicalTrials.gov NCT06306144