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Not yet recruiting NCT06948721

Study of the Participation of People With Aphasia Post Stroke and Their Caregivers in Valladolid Region (Spain)

Observational Stroke Aphasia

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Stroke, Aphasia. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The objective of this study is to determine the level of community participation of people with post-stroke aphasia and their caregivers, as well as the factors that facilitate or interfere with this participation in the Valladolid region (Spain). The main questions that this study aims to answer are: 1. What is the retained activities of the people with aphasia post-stroke? 2. What is the retained activities of the caregivers of people with aphasia post-stroke? 3. What factors influence the community participation of people with aphasia post-stroke and their caregivers?

Primary outcome measures

  • Activity Card Sort [Time frame: Baseline]
Secondary outcome measures (6)
  • The Western Aphasia Battery (WAB) [Time frame: Baseline]
  • Barthel Index (BI) [Time frame: Baseline]
  • Zarit Caregiver Burden Interview (ZBI) [Time frame: Baseline]
  • Six-Minute Walk Test (6MWT) [Time frame: Baseline]
  • Ten-Meter Walk Test (10MWT) [Time frame: Baseline.]
  • Hospital Anxiety and Depression Scale [Time frame: Baseline]

Eligibility criteria

Inclusion criteria

  • Chronic Stroke (stroke onset above six months).
  • Aphasia post stroke.
  • Residents in Valladolid Region.
  • Age over 18 years.
  • Ability to walk equal to or greater than 3 according to the Functional Ambulation Category (FAC).
  • Informed consent acceptance.

Exclusion criteria

  • Stroke onset below of Six months
  • Age under 18 years
  • Both in the case of the person with aphasia and their caregiver, presence of other pathologies that affect functional independence

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06948721 · CIRON

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗