Perceptions of De-implementing Routine Follow-ups After Hip and Knee Arthroplasty
NCT ID: NCT07041528
Last Updated: 2025-06-27
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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NOT_YET_RECRUITING
90 participants
OBSERVATIONAL
2026-09-01
2028-06-01
Brief Summary
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The HAKA trial consists of three different work packages (WPs).The quantitative work packages 1 (WP1) and 2 (WP2) will investigate the 1-year and 10-year follow-up. The qualitative third work package (WP3) will explore and compare the patients' and health care professionals' (HCPs) experiences with, and perceptions about, RFU and COD after total hip and knee arthroplasty. The aim of the overarching HAKA-trial is to safely reduce routine follow-up appointments after total hip or knee arthroplasty and to revise current clinical guidelines accordingly.
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Detailed Description
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Conditions
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Study Design
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OTHER
CROSS_SECTIONAL
Study Groups
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Routine Follow-up (RFU)
Patients planned for total hip or knee surgery who will receive routinely scheduled follow-ups.
No interventions assigned to this group
Check-ups on-demand (COD)
Patients planned for total hip or knee surgery who will receive check-ups on-demand.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
50 Years
ALL
No
Sponsors
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Reinier Haga Orthopedisch Centrum
OTHER
JointResearch
OTHER
Tergooi Medical Center
OTHER
Responsible Party
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Locations
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Tergooi MC
Hilversum, , Netherlands
Countries
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Central Contacts
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Facility Contacts
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References
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National Joint Registry (NJR) Editorial Committee and contributors. 21st Annual Report, Knee Section. 2024
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Related Links
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Published information about HAKA-trial work package 1
Published information about HAKA-trial work package 2
Other Identifiers
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10330042310003
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
N25.014
Identifier Type: -
Identifier Source: org_study_id
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