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Clinical Trials/NL-OMON28267
NL-OMON28267
Not yet recruiting
Not Applicable

Case management after acquired brain injury

Stichting In-Tussen0 sites152 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Stichting In-Tussen
Enrollment
152
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Stichting In-Tussen

Eligibility Criteria

Inclusion Criteria

  • In order to be eligible to participate in this study, patients (both early and late inclusion) must meet all of the following criteria:
  • Acquired brain injury objectified by medical specialist
  • Aged 18 years or older
  • Living in the community prior to the injury
  • Discharged home after hospital/rehabilitation
  • Sufficient command of the Dutch language
  • Access to a computer and the internet (monitoring tool and questionnaires)
  • Willing and able to give informed consent
  • Primary caregivers (the informal caregiver who takes primary responsibility to care for the person with brain injury) of eligible patients are eligible when they are aged 18 years or older, have sufficient command of the Dutch language, have access to a computer and internet and are willing and able to give informed consent. Primary caregivers can only participate if the person with brain injury is participating.

Exclusion Criteria

  • A potential subject will be excluded from participation in this study when they are unable to consent to participation or when they are discharged to hospice care, nursing home for long term care, or a long\-term care hospital. Participants with degenerative disorders (e.g. Parkinson’s disease, dementia) are excluded because of the progressive course of the disease, patients with a diagnosis related to neuro\-oncology will be excluded as well, since an intensive care trajectory is already in place for these patients.

Outcomes

Primary Outcomes

Not specified

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