RecruitingNot Applicable

Home-based Cognitive Strategy Training for Daily Living in Adults With Chronic Stroke

France18 participantsStarted 2026-01-05

Plain-language summary

This pilot experimental study aims to describe the feasibility of a cognitive strategy training protocol : PRPP-I, in activities of daily life across home-based setting for adults with chronic stroke for improvement of independence and quality of life. Aditionnally to examine preliminary effectiveness of PRPP-I protocol within a home-based setting on functional cognitive strategies, independence, quality of life and career burden.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Patient's Main Eligibility criteria: * Adult over 18 years of age; * cognitive deficits (or Acquired Brain Injury) diagnosed due to ischemic or hemorrhagic, hemispheric or brainstem stroke, confirmed by brain imaging longer than 6 months; * Patient with mild (\<26/30 or \<25/30 for patients aged 71-85 yr) or moderate (\[18-25\]/30) cognitive impairment, measured by the Montreal Cognitive Assessment test ; * adults living in a home or community-based setting; * Patient with a non-professional caregiver; Patient's Main Exclusion criteria * Neurological pathology other than stroke or psychiatric disorder; * Significant cognitive impairment, according to MoCA score \<18/30; * Patient with severe aphasia, Boston Diagnostic Aphasia Examination score \>2

What they're measuring

Feasability

Timeframe: From enrollment to the end of intervention at 4 weeks

Trial details

NCT IDNCT07084025

SponsorUniversity Hospital, Toulouse

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2027-12-31

Contact for this trial

Margot MORIN

05 61 77 73 47 morin.mar@chu-toulouse.fr

View on ClinicalTrials.gov More Stroke trials