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NCT07084025Recruiting

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

Feasibility of Home-based Cognitive Strategy Training for Independence of Activities of Daily Living in Adults With Chronic Stroke

Source: ClinicalTrials.gov · Last updated 8 May 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
18 (estimated)
First submitted
16 Jul 2025
Start date
5 Jan 2026
Primary completion date
31 Dec 2027
Lead sponsor
University Hospital, Toulouse
Diseases
Stroke
NCT number
NCT07084025

What you commit to

  • Study type: Interventional
  • Planned participants: 18
  • From 5 Jan 2026 to the primary completion date, 31 Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Criteria the registry did not label

  • 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

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University Hospital of Toulouse
Coordinator of this site? Confirm its status
ToulouseFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.