Study Results
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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UNKNOWN
NA
75 participants
INTERVENTIONAL
2022-08-02
2023-08-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Control
Post-test satisfaction
Telephone Follow-up
Telephone Follow-up within 72 hours to discuss psycho education, discharge planning and clarify any questions they may have.
Experimental
Treatment and satisfaction
Telephone Follow-up
Telephone Follow-up within 72 hours to discuss psycho education, discharge planning and clarify any questions they may have.
Interventions
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Telephone Follow-up
Telephone Follow-up within 72 hours to discuss psycho education, discharge planning and clarify any questions they may have.
Eligibility Criteria
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Inclusion Criteria
* Age of majority
* Competent.
Exclusion Criteria
* Under 18
* Admitted to the hospital
18 Years
ALL
Yes
Sponsors
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Brandon University
OTHER
Responsible Party
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Alana Prejet
Principal Investigator
Principal Investigators
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Alana E Prejet, BScPN, BA
Role: PRINCIPAL_INVESTIGATOR
Brandon University
Locations
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St. Boniface Hospital
Winnipeg, Manitoba, Canada
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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BrandonU
Identifier Type: -
Identifier Source: org_study_id
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