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The Outcome of Three Weeks Rehabilitation in Patients With a Total Hip or Knee Replacement Experiencing Persistent Physical Impairments

The Outcome of Three Weeks Rehabilitation in Patients With a Total Hip or Knee Replacement Experiencing Persistent Physical Impairments

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07105657
Acronym
Rehab-hip-knee
Enrollment
84
Registered
2025-08-06
Start date
2025-08-25
Completion date
2027-12-31
Last updated
2025-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hip Osteoarthritis, Knee Osteoarthristis

Keywords

total hip replacement, rehabilitation, hip osteoartritis, knee osteoarthritis, total knee replacement

Brief summary

Patients with total hip or knee replacement experiencing persistant problems are offered 3 weeks of intensive rehabilitation.

Detailed description

Outcomes before, at the end of treatment and at 6 months follow up will be investigated. Data will be handled separately for the two groups of patients: 42 with a total hip replacement and 42 with a total knee replacement. Specific and generic outcomes will be collected.

Interventions

OTHERRehabilitation

Three weeks intensive rehabilitation where patients undergo group-based and individualised rehabilitation focusing at improving pain, function and quality of life for the patient

Sponsors

VIA University College
CollaboratorOTHER
Horsens Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

\- Patients with a total hip or knee replacement admitted for intensive rehabilitation

Exclusion criteria

* Patients unable to understand Danish * Unable to participate in physical tests * Unable to understand questionaires * Unable to participate i 6 months follow up

Design outcomes

Primary

MeasureTime frameDescription
HOOS/KOOS quality of life (0-100 score)Change from baseline (0) to 3 weeksHip or knee related quality of life
Sit-to-stand testChange from baseline (0) to 3 weeksNumber of completed sit to stands in 30 seconds
HOOS/KOOS pain (0-100 score)Change from baseline (0) to 3 weeksHip or knee related pain
HOOS/KOOS ADL (0-100 score)Change from baseline (0) to 3 weeksHip or knee related activities of daily living

Secondary

MeasureTime frameDescription
The 5-level EQ-5D version (EQ-5D-5L) (0-5 scale)Change from baseline (0) to 3 weeksEQ5D5L scores
EQ5D VAS (0-100 scale)Change from baseline (0) to 3 weeksEQ5D Vas overall health
HOOS/KOOS symptoms (0-100 score)Change from baseline (0) to 3 weeksHip or knee related symptoms
6 minute walk testChange from baseline (0) to 3 weeksThe distance a patient can walk in 6 minutes
40 meter fast paced walk testChange from baseline (0) to 3 weeksThe time a patient uses walking 40 meters fast
Stair testChange from baseline (0) to 3 weeksThe time a patient uses to ascend and decend a staircase
HOOS/KOOS sport/rec (0-100 score)Change from baseline (0) to 3 weeksHip or knee related sport/rec
Patient acceptable symptom state (yes/no)3 weeks follow upPatients are asked with a single question if their current symptom state is acceptable
Pain catastrophising scale (0-52 score)BaselineCurrent level of pain catastrophising with 0 being the best
Global rating of change (0-11 score)Change from baseline to 3 weeksLikert scale where patients indicate their overall rating of change since the beginning of the intervention

Other

MeasureTime frameDescription
Patient acceptable symptom state (yes/no)BaselinePatients are asked with a single question if their current symptom state is acceptable
Employment status (yes/no/part time)Baseline

Countries

Denmark

Contacts

Primary ContactSigne Kierkegaard-Brøchner, PhD
signkier@rm.dk004578427882

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026