NCT07105657

Brief Summary

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

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
84

participants targeted

Target at P50-P75 for all trials

Timeline
20mo left

Started Aug 2025

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress30%
Aug 2025Dec 2027

First Submitted

Initial submission to the registry

July 30, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

August 6, 2025

Completed
19 days until next milestone

Study Start

First participant enrolled

August 25, 2025

Completed
2.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2027

Last Updated

August 26, 2025

Status Verified

August 1, 2025

Enrollment Period

2.4 years

First QC Date

July 30, 2025

Last Update Submit

August 25, 2025

Conditions

Hip OsteoarthritisKnee Osteoarthristis

Keywords

total hip replacementrehabilitationhip osteoartritisknee osteoarthritistotal knee replacement

Outcome Measures

Primary Outcomes (8)

  • HOOS/KOOS pain (0-100 score)

    Hip or knee related pain

    Change from baseline (0) to 3 weeks

  • HOOS/KOOS ADL (0-100 score)

    Hip or knee related activities of daily living

    Change from baseline (0) to 3 weeks

  • HOOS/KOOS quality of life (0-100 score)

    Hip or knee related quality of life

    Change from baseline (0) to 3 weeks

  • HOOS/KOOS pain (0-100 score)

    Hip or knee related pain

    Change from 3 weeks to 7 months

  • HOOS/KOOS ADL (0-100 score)

    Hip or knee related activities of daily living

    Change from 3 weeks to 7 months

  • HOOS/KOOS quality of life (0-100 score)

    Hip or knee related quality of life

    Change from 3 weeks to 7 months

  • Sit-to-stand test

    Number of completed sit to stands in 30 seconds

    Change from baseline (0) to 3 weeks

  • Sit-to-stand test

    Number of completed sit to stands in 30 seconds

    Change from 3 weeks to 7 months

Secondary Outcomes (21)

  • Patient acceptable symptom state (yes/no)

    3 weeks follow up

  • Patient acceptable symptom state (yes/no)

    7 months follow up

  • Pain catastrophising scale (0-52 score)

    Baseline

  • Pain catastrophising scale (0-52 score)

    3 weeks

  • Pain catastrophising scale (0-52 score)

    7 months

  • +16 more secondary outcomes

Other Outcomes (3)

  • Patient acceptable symptom state (yes/no)

    Baseline

  • Employment status (yes/no/part time)

    Baseline

  • Employment status (yes/no/part time)

    7 months

Study Arms (2)

Intervention group hip

Patients with a total hip replacement undergoing rehabilitation

Other: Rehabilitation

Intervention group knee

Patients with a total hip replacement undergoing rehabilitation

Other: Rehabilitation

Interventions

RehabilitationOTHER

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 hipIntervention group knee

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients who have a total hip or knee replacement experiencing persistant problems, hence are admitted to a 3 week intensive rehabilitation period.

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Horsens Regional Hospital

Brædstrup, Denmark

RECRUITING

MeSH Terms

Conditions

Osteoarthritis, HipOsteoarthritis, Knee

Interventions

Rehabilitation

Condition Hierarchy (Ancestors)

OsteoarthritisArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic Diseases

Intervention Hierarchy (Ancestors)

AftercareContinuity of Patient CarePatient CareTherapeuticsHealth ServicesHealth Care Facilities Workforce and Services

Central Study Contacts

Signe Kierkegaard-Brøchner, PhD

CONTACT

004578427882signkier@rm.dk

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Ass. prof.

Study Record Dates

First Submitted

July 30, 2025

First Posted

August 6, 2025

Study Start

August 25, 2025

Primary Completion (Estimated)

December 31, 2027

Study Completion (Estimated)

December 31, 2027

Last Updated

August 26, 2025

Record last verified: 2025-08

Locations

DK(1)