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Knee Pain Nurse Led Package of CareTrial

NCT03670706 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1806

Last updated 2021-09-21

No results posted yet for this study

Summary

1. To develop a training package for nurse-led management of knee osteoarthritis (OA), incorporating information about OA and core non-pharmacologic and pharmacologic principles of management of OA as recommended in the National Institute for Clinical Excellence and Health (NICE) guidelines for management of OA
2. To evaluate fidelity of delivery of individual components of this complex package of care for knee pain
3. To assess the acceptability of the intervention by exploring participant satisfaction with nurse-led complex package of care of knee pain.
4. To explore and resolve possible challenges to delivery of individual components within a complex package
5. To examine the feasibility of a definitive cohort randomised controlled trial of nurse-led care versus usual care of knee pain in terms of recruitment rate, drop-out rate, reasons for dropping out and completeness of outcome data
6. To explore whether such a trial should provide analgesia before non-pharmacologic interventions or vice versa

Conditions

  • Osteoarthritis, Knee
  • Pain, Joint

Interventions

BEHAVIORAL

Exercise

Package of care

OTHER

analgesic optimisation

optimisation

Sponsors & Collaborators

  • University of Nottingham

    lead OTHER

Principal Investigators

  • Abhishek Abhishek · University of Nottingham/ Nottingham University NHS Trust

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-11-26
Primary Completion
2021-07-05
Completion
2021-07-05

Countries

  • United Kingdom

Study Locations

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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 NCT03670706 on ClinicalTrials.gov