Strengthening the Interdisciplinary and Inter Sectoral Collaboration in Stroke Rehabilitation Through Application of FIM
Application of the Functional Independence Measure® (FIM) With the Aim of Strengthening the Interdisciplinary and Inter Sectoral Collaboration in Stroke Rehabilitation - a Mixed Methods Multicenter Study
1 other identifier
observational
20
1 country
2
Brief Summary
This study seeks to explore ways to strengthening the interdisciplinary and inter sectoral collaboration in stroke rehabilitation through the application of Functional Independence Measure® (FIM) and common interdisciplinary patient related tasks. The study will be evaluated through interviews with staff, participant observation and quantitative patient data.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Jan 2021
Shorter than P25 for all trials
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 21, 2020
CompletedFirst Posted
Study publicly available on registry
September 25, 2020
CompletedStudy Start
First participant enrolled
January 25, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
January 15, 2022
CompletedFebruary 8, 2022
January 1, 2022
9 months
September 21, 2020
January 24, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Functional Independence Measure® (FIM)
FIM® measures disability by the amount of assistance needed during daily activities. FIM consists of 18 items, 13 in the motor and 5 in the cognitive domain. The scale ranges from 18-126.
Admittance to hospital to discharge from a facility in the municipality, approx. 4 months.
Eligibility Criteria
Patients with a postal code in the Municipality of Copenhagen, hospitalized with stoke in Bispebjerg Hospital.
You may qualify if:
- Diagnosed with stroke (i61 and i63).
- Hospitalized for stroke rehabilitation in Bispebjerg Hospital.
- Hospitalized in Regional Beds (given to patients with a brain damage of moderate to severe character who receives intensive rehabilitation) within 1 week of arrival at the hospital.
- Living in the Municipality of Copenhagen.
- Consenting to participate.
You may not qualify if:
- Discharged to other facility than Neurorehabilitering Copenhagen.
- Unable to participate in neuro-rehabilitation in more than one week continuously due to e.g. infection.
- Qualitative study participants:
- Interview Study Participants:
- Interdisciplinary staff at Bispebjerg Hospital Neurological Rehabilitation Department and Neurorehabilitering Copenhagen.
- Participant in the project group experimenting with the FIM
- Consenting to participate.
- Participant observation:
- Interdisciplinary staff at Bispebjerg Hospital Neurological Rehabilitation Department and Neurorehabilitering Copenhagen.
- Participant in FIM team meetings.
- Consenting to participate.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Neurorehabilitering Copenhagen
Copenhagen, Hellerup, 2900, Denmark
Bispebjerg Hospital
Copenhagen, København NV, 2400, Denmark
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Irene Conradsen, Master
Neurorehabilitering Copenhagen
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Target Duration
- 4 Months
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Consultant
Study Record Dates
First Submitted
September 21, 2020
First Posted
September 25, 2020
Study Start
January 25, 2021
Primary Completion
November 1, 2021
Study Completion
January 15, 2022
Last Updated
February 8, 2022
Record last verified: 2022-01