Validation of PROMIS pain interference and physical functioning in patients undergoing total hip and total knee arthroplasty

Psychometric properties of the PROMIS Pain Interference and Physical Functioning in patients undergoing total hip and total knee arthroplasty

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON19972

Enrollment

400

Registered

2021-03-12

Start date

2021-06-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

Total Hip Arthroplasty (THA) or Total Knee Arthroplasty (TKA)

Interventions

None

Eligibility

Inclusion criteria

Inclusion criteria: - Age =18 years - Primary arthroplasty - Total hip arthroplasty: pre-operatively, 3, 6 or 12 months post-operatively - Total knee arthroplasty: pre-operatively, 6 or 12 months post-operatively.

Exclusion criteria

Exclusion criteria: - Unicondylar knee arthroplasty - Hip arthroplasty after femoral neck fracture - Unable to independently fill out questionnaires - Insufficient knowledge of the Dutch language - No internet facilities

Design outcomes

Primary

Measure	Time frame
Smallest detectable change of the PROMIS-CAT, PROMIS–Shortforms and the currently used outcome measurement instruments in patients undergoing THA or TKA	—

Secondary

Measure	Time frame
Psychometric properties of the PROMIS-CAT, PROMIS-Shortforms and the currently used outcome measurement instruments in patients undergoing THA or TKA o Reliability o Internal consistency o Measurement error o Construct validity o Responsiveness - Burden for patients (the number of items needed) - Interpretability of the scores	—

Contacts

Public ContactNienke Wolterbeek

St. Antonius Ziekenhuis

n.wolterbeek@antoniusziekenhuis.nl0883202325

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)