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StrokeFinPostStrokeNCT06575907

Health, Functioning, Work, and Experiences of Social and Health Services of Persons With Stroke

An observational study of Stroke and Health, Subjective, run by The Finnish Association of People with Physical Disabilities at 1 site in Finland.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

The purpose of the Health, functioning, work, and experiences of social and health services of persons with stroke study (FinPostStroke) is to identify factors related to self-reported health, functioning, work, inclusion, and accessibility of social and health services, and how such factors are interconnected in… Read more about this study

Who is it for?
Ages 18 years and older
How many people
2,000 participants
Where
1 siteFinland
Study dates
22 May 2026to Sep 2026
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Adults with acute ischemic stroke, subarachnoid hemorrhage, or intracerebral hemorrhage that have been treated either in North Savo or Uusimaa hospitals in 2018-2022.

Who may be able to join

  • treated for acute stroke (ICD-10 codes I60-61, I63-64) in North Savo or Uusimaa region of Finland between January 2020 and December 2022
  • lives currently in North Savo or Uusimaa region of Finland
  • 18 years or older at the time of stroke

Who cannot join

  • missing address
  • deceased

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Finland1 site
  • The Finnish Association of People with Physical Disabilities

    Helsinki, Uusimaa, 00280

Other trials in Finland

About this study

The purpose of the Health, functioning, work, and experiences of social and health services of persons with stroke study (FinPostStroke) is to identify factors related to self-reported health, functioning, work, inclusion, and accessibility of social and health services, and how such factors are interconnected in Finnish adults several years after stroke. Participants will be targeted from hospital registries and recruited by postal mail.

This cross-sectional explorative observational study is based on register data and postal survey. The survey questionnaire includes several valid patient-reported outcome measures. The study will provide useful information for developing social and health services for people several years after stroke.

Read the detailed description

The purpose of the Health, functioning, work, and experiences of social and health services of persons with stroke (FinPostStroke) study is to identify factors related to self-reported health, functioning, work, inclusion, and accessibility of social and health services, and how such factors are interconnected in Finnish adults several years after stroke. The International Classification of Functioning, Disability and Health (ICF) is used as a structured framework.

Adults with ischemic stroke, subarachnoid hemorrhage, or intracerebral hemorrhage will be targeted from Kuopio and Helsinki University Hospitals' patient registries. The survey data is planned to be collected with postal questionnaire by May 2026. The questionnaire includes several valid patient-reported outcome measures to assess health and functioning, work and income, inclusion, and social and health services. Participants will be recruited by postal mail with an invitation letter and study information attached to the questionnaire. All participants are expected to give written informed consent prior to the study.

The study will provide useful information for developing social and health services for people several years after stroke. We plan to publish at least four peer-reviewed articles along with common articles and texts concerning self-reported health, functioning, work, inclusion, and accessibility of social and health services among Finnish adults with stroke.

Being tested
no intervention
Keywords
ICF, Survey, Stroke, Health, Functioning, Work, Inclusion, Health and social services
Medical subject headings
Stroke, Cardiovascular Diseases, Central Nervous System Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • no interventionOther

    no intervention

Study groups in NCT06575907
Study groupRoleWhat they receive
Stroke survivors living in North Savo region of FinlandIndividuals who suffered a stroke in 2020-2022
Receives: Other: no intervention
Stroke survivors living in Uusimaa region of FinlandIndividuals who suffered a stroke in 2020-2022
Receives: Other: no intervention

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. PROMIS® Global Health

    The Patient-Reported Outcomes Measurement Information System (PROMIS®) Global Health consists of 10 items with 5-point rating scale. It is used to assess overall health, physical health, mental health, social health, fatigue, and pain.

    Measured: 7 days

  2. 12-item WHODAS 2.0

    The 12-item World Health Organization Disability Schedule 2.0 (WHODAS) measures functioning. It consists of 12 items with 5-point rating scale (0-4), sum score ranging from 0 to 48. Higher score means more disability. It is used to assess cognition, mobility, self-care, getting along, life activities, and participation.

    Measured: 30 days

  3. EQ-5D-5L

    The EQ-5D-5L is a self-reported instrument measuring health status. It consists five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression, that are evaluated through five statements/levels. The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state (5-digit health state profile) that represents the level of reported problems on each of the five dimensions of health. In addition, EQ-5D uses Visual analogue Scale (VAS) for "We would like to know how good or bad your health is TODAY".

    Measured: Baseline

  4. Experiences of Social Inclusion Scale, ESIS

    Experiences of Social Inclusion Scale (ESIS) consists of 10 claims with 5-point Likert scale (1-5). The sum score of 10-50 is converted to a scale of 0 to 100. Higher score means stronger experience of inclusion. It is used to assess the experience of meaningfulness, belief in action possibilities and the perceived quality of social interaction.

    Measured: Baseline

  5. Health and social services

    "Health and social services" consists of 24 semistructured questions about health and social services chosen from the National Health Finland Survey.

    Measured: 1 year

  6. Work and income

    "Work and income" consists of 14 semistructured questions about work and income chosen from the International Spinal Cord Injury Survey.

    Measured: 30 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Aug 2024
  2. Study start22 May 2026
  3. Primary completion31 Aug 2026
  4. Study completionSep 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
2,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06575907
Sponsor's protocol ID
pr42115
Acronym
FinPostStroke
Status last verified
Sep 2026
First submitted
21 Aug 2024
Last updated
10 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Stroke and Health, Subjective, run by The Finnish Association of People with Physical Disabilities at 1 site in Finland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 10 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Finland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

PROMIS® Global Health (time frame: 7 days). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Sep 2026.

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