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Stroke in North of Norway and Denmark. A Prospective Cohort Study.

NCT ID: NCT02311426

Last Updated: 2021-11-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

1000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-03-31

Study Completion Date

2022-09-30

Brief Summary

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The study is a comparative effectiveness study with comparision of two cohorts of patients with stroke in North of Norway and in Denmark. At baseline information is collected from the stroke registries in both countries. Time points for follow up are at 3 and 12 months post-stroke. Data are collected from medical charts and with use of telephone interview in addition to self-report questionnaires. The study will provide information about functional status, health related quality of life and rehabilitation needs. Information about rehabilitation services in both countries are collected and compared, and analysed in relation to patients outcome.

Detailed Description

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Conditions

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Stroke

Keywords

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Rehabilitation; Functional outcome

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Norway

500 consecutive patients with stroke from the stroke units at the University Hospital of North Norway located in the cities Narvik, Harstad and Tromsø.

At baseline 155 patients with first ever stroke were registered. At 3 and 12 months follow-up 135-155 patients were enrolled.

Observational study

Intervention Type OTHER

Function, health related quality of life and rehabilitation needs will be analysed in the two country region groups

Denmark

500 consecutive patients from the stroke unit at Århus Hospital in Denmark. At baseline 402 patients with first ever stroke were included. At 3 and 12 months follow-up 318/ 170 patients were enrolled.

Observational study

Intervention Type OTHER

Function, health related quality of life and rehabilitation needs will be analysed in the two country region groups

Interventions

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Observational study

Function, health related quality of life and rehabilitation needs will be analysed in the two country region groups

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Verified stroke. Admitted to stroke unit.

Exclusion Criteria

* Patients outside the regions excluded.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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St. Olavs Hospital

OTHER

Sponsor Role collaborator

University Hospital of North Norway

OTHER

Sponsor Role lead

Responsible Party

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Audny Anke

MD, PhD, Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Audny Anke, MD PhD

Role: PRINCIPAL_INVESTIGATOR

University Hospital of North Norway

Locations

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University Hospital of North Norway

Tromsø, , Norway

Site Status

Countries

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Norway

Other Identifiers

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SFP1175-14

Identifier Type: -

Identifier Source: org_study_id