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What Matters to Patients With Severe Hip or Knee Osteoarthritis?

NCT05972525 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 615

Last updated 2026-03-12

No results posted yet for this study

Summary

This clinical trial aims to investigate if shared decision-making, and the use of an in-consultation patient decision aid (PtDA), increases the decisional quality and therefore treatment satisfaction and outcome of patients with severe hip or knee osteoarthritis.

Finally, an evaluation will be conducted on patient-reported outcomes on pain, physical function, quality of life (QoL), and patient satisfaction, up to one year after surgery.

Conditions

Interventions

BEHAVIORAL

Shared decision-making supported by an in-consultation PtDA to patients with severe osteoarthritis in their hip or knee

The intervention group has been involved in the development process of the PtDA. After receiving a training course in SDM and the use of a PtDA, the surgeons will practice SDM supported by an in-consultation PtDA during the consultations with the participant.

Sponsors & Collaborators

  • Odense University Hospital

    collaborator OTHER

  • Vejle Hospital

    lead OTHER

Principal Investigators

  • Trine Ahlmann, PhD stud · Vejle Hospital

  • Claus Varnum, Ass.Prof.MD · Vejle Hospital

  • Martin Lindberg-Larsen, Ass.Prof.MD. · Odense University Hospital

  • Charlotte Myhre Jensen, Ass.Prof.RN · Odense University Hospital

  • Karina Dahl Steffensen, Prof.MD. · Vejle Hospital

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-10-11
Primary Completion
2024-11-29
Completion
2026-07-11

Countries

  • Denmark

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05972525 on ClinicalTrials.gov