Clinical Trials Directory

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

TypeNameDescription
OTHERReturn to Sport testbatteryAt 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.