NCT04564820

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Jan 2021

Shorter than P25 for all trials

Geographic Reach
1 country

2 active sites

Status
completed

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

Completed
4 days until next milestone

First Posted

Study publicly available on registry

September 25, 2020

Completed
4 months until next milestone

Study Start

First participant enrolled

January 25, 2021

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2021

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 15, 2022

Completed
Last Updated

February 8, 2022

Status Verified

January 1, 2022

Enrollment Period

9 months

First QC Date

September 21, 2020

Last Update Submit

January 24, 2022

Conditions

Keywords

StrokeRehabilitationInterdisciplinaryFunctional Independence MeasureFIM

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

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

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

Location

Bispebjerg Hospital

Copenhagen, København NV, 2400, Denmark

Location

MeSH Terms

Conditions

Stroke

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular Diseases

Study Officials

  • Irene Conradsen, Master

    Neurorehabilitering Copenhagen

    PRINCIPAL INVESTIGATOR

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

Locations