nderstanding Knee Osteoarthritis Pain Experiences

Not Applicable

Completed

• Conditions: Knee Osteoarthritis; Musculoskeletal - Osteoarthritis

• Registration Number: ACTRN12621000930886
• Lead Sponsor: Otago Medical Research Foundation

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2021-07-15
• Study Completion: 2022-03-25
• Last Update Posted: 27 June 2022

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 86

Inclusion Criteria

Those with a diagnosis of knee osteoarthritis who experience knee pain on most days for at least three months will be eligible for inclusion.

Exclusion Criteria

Participants will be excluded if they are non-English speaking, are unable to use a smartphone, have an auto-immune condition or other form of inflammatory arthritis, have uncontrolled hypertension, skin conditions, lower limb sensory loss, pregnant or within six months postpartum, have undergone or are scheduled for total knee arthroplasty, have sustained a lower limb injury in the last six months (or still recovery), have a neurological condition, impaired cognition or psychiatric illness.

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain[Cross sectional at baseline and prospective longitudinally at 2-weeks (including Ecological Momentary Assessment (EMA)) and 9-weeks via pain patient-reported measures (Brief Pain Inventory).];Function[Cross sectional at baseline and prospective longitudinally at 2-weeks (including EMA) and 9-weeks via functional patient-reported measures (Knee Injury and Osteoarthritis Outcome Score)];Pain interference[Cross-sectional, two-weeks and nine-weeks post assessment. This will be measured using the EMA pain interference item and the Brief Pain Inventory. ]