Trials / Completed
CompletedNCT05119088
Development of a Test Battery for Measurement of Knee Function in Patients With Patellar Instability
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 120 (actual)
- Sponsor
- Haraldsplass Deaconess Hospital · Academic / Other
- Sex
- All
- Age
- 13 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
About six months after patella stabilizing surgery postoperative restrictions are commonly lifted and patients may consider whether a return to activity/sports is feasible. Currently, there are no evidence-based criteria to determine a patients readiness for sports and/or activity (RTS) following stabilizing surgery. The purpose of this project was therefore to investigate the feasibility of a test battery to evaluate knee function in postoperative follow-up evaluation - and in RTS decisions - for patients with patellar instability. Banff Patellofemoral Instability Instrument 2.0 and Norwich Patellar Instability Score is being translated and validatend in a Norwegian population. Furter is patients experience of living with patellar instability explored.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Return to Sport testbattery | At baseline, approximately 3 weeks before surgery and 6 months after surgery: patients conduct a testbattery consisting of 2 PROMs: the NPI-No and BPII2.0-No together with three physical tests: isokinetic strength tests, hop tests and Y-balance test. For the cross-cultural validation of NPI and BPII2.0 patients also conduct KOOS, IKDC 2000 and Tampa Scale. |
Timeline
- Start date
- 2021-01-04
- Primary completion
- 2023-02-20
- Completion
- 2023-02-20
- First posted
- 2021-11-12
- Last updated
- 2023-03-01
Locations
1 site across 1 country: Norway
Source: ClinicalTrials.gov record NCT05119088. Inclusion in this directory is not an endorsement.