NCT05829421Completed

Addressing Problems in Managing Daily Tasks Due to Poststroke Cognitive Impairments

Feasibility of a Neuropsychologically Informed Occupational Therapy Intervention Targeting Decreased Ability to Perform Activities of Daily Living in People With Poststroke Cognitive Impairment

Source: ClinicalTrials.gov · Last updated 5 Dec 2025

Brief summary (registry, in English)

The purpose of this study is to investigate feasibility aspects of an intervention targeting problems in managing daily tasks due to mild-to-moderate poststroke cognitive impairments. We will specifically address uncertainties related to intervention content and delivery, and trial design and conduct.

Status (registry): Completed
Study type: Interventional
Enrollment: 8 (actual)
First submitted: 6 Mar 2023
Start date: 25 May 2023
Primary completion date: 29 Mar 2024
Lead sponsor: Emma Ghaziani
Diseases: Stroke
NCT number: NCT05829421

What you commit to

Study type: Interventional
Participants enrolled: 8
From 25 May 2023 to the primary completion date, 29 Mar 2024
4 sites 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.

Other illness

psychiatric conditions causing difficulties or preventing participation, as evaluated by the recruiting health care professional(s)

Other

communication problems causing difficulties or preventing participation, as evaluated by the recruiting healthcare professional(s)
- CAREGIVERS:
-communication problems or other issues causing difficulties in participation as evaluated by the recruiting healthcare professional(s).
Patients without a close carer will not be excluded.
CLINICAL STAFF:
\- unable to to follow a preliminary English version of the intervention manual.

Who the study is looking for

first-ever symptomatic stroke,
age ≥ 18 years,
residence in Frederiksberg Municipality, Denmark,
independent in pre-stroke everyday life (≤ 2 points on the modified Rankin Scale, mRS),
experiencing problems in performing ADLs due to cognitive impairment; these problems are expected to still be present at hospital discharge,
medical condition allows commencement of rehabilitation focused on ADL and cognition
fully aware or mild-to-moderate unawareness of deficits (≤ 2 points on the Bisiach Anosognosia Scale, BAS),
a global cognitive function corresponding to ≥ 17 points on the Montreal Cognitive Assessment, MoCA,
≤ 10 points on the depression subscale of the Hospital Anxiety and Depression Scale, HADS,
able to provide informed consent, as evaluated by the recruiting healthcare professional(s),
logistically possible to perform baseline assessments and create an individualised intervention plan during hospital stay
provides informed consent
appointed as close carer (by a patient who consented to participate),
age ≥18y,
provides informed consent.
appointed as local project managers, or OTs or NPs who conduct assessments or deliver the intervention in the participating centres,
provides informed consent.

Criteria the registry did not label

PATIENTS:

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

Full criteria on ClinicalTrials.gov

Sites (4)

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

Site	City	Country	Site status
Bispebjerg and Frederiksberg Hospital Coordinator of this site? Confirm its status	Copenhagen	Denmark	Unknown status
the Inpatient Rehabilitation Centre Coordinator of this site? Confirm its status	Frederiksberg	Denmark	Unknown status
Neurorehabilitation Centre Østervang Coordinator of this site? Confirm its status	Frederiksberg	Denmark	Unknown status
the Day Rehabilitation Centre Coordinator of this site? Confirm its status	Frederiksberg	Denmark	Unknown status

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