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Addressing Problems in Managing Daily Tasks Due to Poststroke Cognitive Impairments

NCT05829421 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 8

Last updated 2025-12-05

No results posted yet for this study

Summary

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.

Conditions

Interventions

OTHER

Impairment-specific occupational therapy (OT) intervention

In parallel with standard practice, patients receive an OT intervention adapted to the specific underlying cognitive impairments that are likely to disturb their performance of ADLs. The intervention is individualised through a 3-step process: a) a list of dysfunctional ADL process skills is forwarded by the OT to the neuropsychologist (NP), b) the NP identifies the cognitive impairments which are most likely to cause the dysfunctional ADL process skills through a cognitive assessment, c) based on the identified cognitive impairments, the NP and the OT select in collaboration the cognitive strategies that are most likely to benefit the individual patient from a pre-prepared intervention manual. Because of the large heterogeneity in how cognitive impairments impact on ADL performance, the exact way of implementing the selected cognitive strategies into the practice of the individual patient is left to the OT´s clinical judgement.

Sponsors & Collaborators

  • Rigshospitalet, Denmark

    collaborator OTHER

  • The Day Rehabilitation Centre, Frederiksberg Municipality, Denmark

    collaborator UNKNOWN

  • The Inpatient Rehabilitation Centre, Frederiksberg Municipality, Denmark

    collaborator UNKNOWN

  • Neurorehabilitation Centre Østervang, Frederiksberg Municipality, Denmark

    collaborator UNKNOWN

  • Emma Ghaziani

    lead OTHER

Principal Investigators

  • Hanne Christensen, Professor · Bispebjerg and Frederiksberg Hospital

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-05-25
Primary Completion
2024-03-29
Completion
2025-10-01

Countries

  • Denmark

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05829421 on ClinicalTrials.gov