Home-based cognitive strategy training to support daily living after chronic stroke

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This pilot interventional study delivers the Perceive, Recall, Plan and Perform-Intervention (PRPP-I) protocol as task-based cognitive strategy training during real-life activities in participants' homes. It targets adults more than six months after ischemic or hemorrhagic stroke with mild to moderate cognitive impairment measured by the MoCA. The study will report feasibility outcomes (acceptability, adherence, and practicality of home delivery) and preliminary effectiveness on functional cognitive strategy use, independence in activities of daily living, quality of life, and caregiver burden. Participants receive individualized training during everyday tasks with outcome measures collected before and after the intervention.

Why it matters

Who can join: the full rules

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

Where it's running

• University Hospital of Toulouse
  Toulouse, France Recruiting

Study contacts

• Study coordinator: Margot MORIN
• Email: morin.mar@chu-toulouse.fr
• Phone: 05 61 77 73 47

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.