The Outcome of Three Weeks Rehabilitation in Patients With a Total Hip or Knee Replacement Experiencing Persistent Physical Impairments
NCT ID: NCT07105657
Last Updated: 2025-08-26
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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RECRUITING
84 participants
OBSERVATIONAL
2025-08-25
2027-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Intervention group hip
Patients with a total hip replacement undergoing rehabilitation
Rehabilitation
Three weeks intensive rehabilitation where patients undergo group-based and individualised rehabilitation focusing at improving pain, function and quality of life for the patient
Intervention group knee
Patients with a total hip replacement undergoing rehabilitation
Rehabilitation
Three weeks intensive rehabilitation where patients undergo group-based and individualised rehabilitation focusing at improving pain, function and quality of life for the patient
Interventions
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Rehabilitation
Three weeks intensive rehabilitation where patients undergo group-based and individualised rehabilitation focusing at improving pain, function and quality of life for the patient
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Unable to participate in physical tests
* Unable to understand questionaires
* Unable to participate i 6 months follow up
18 Years
ALL
No
Sponsors
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VIA University College
OTHER
Horsens Hospital
OTHER
Responsible Party
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Jeppe Lange
Ass. prof.
Locations
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Horsens Regional Hospital
Brædstrup, , Denmark
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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1-16-02-329-25
Identifier Type: -
Identifier Source: org_study_id
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