Knee Osteoarthritis Clinical Trial
Official title:
A Feasibility Randomised Controlled Trial of the Implementation in Malaysian Healthcare Context of the ESCAPE-pain Programme for Patients With Knee Osteoarthritis
The overall aim of this study is to develop an evidence based exercise programme for the management of knee osteoarthritis which is feasible and acceptable to patients and healthcare professionals in Malaysia. The chosen programme was identified through a systematic literature search and is the programme developed by Hurley et al. in 2007. This programme will be evaluated through mixed-methods sequential exploratory design research study guided by the United Kingdom (UK) Medical Research Council guidance and framework. It involves two phases of data collection. The first phase (already completed) comprised a qualitative study aimed at exploring the beliefs and attitudes of Malaysian people that would need to be taken into account when adapting the evidence based ESCAPE-pain (acronym for 'Enabling Self-management and Coping with Arthritic pain using Exercise) programme for implementation in the context of Malaysian healthcare system. The second phase will be conducted to evaluate the feasibility of trialling ESCAPE-pain programme in Malaysia.
In Malaysia, functional limitations and impaired daily living activities affect patients with
knee osteoarthritis (OA) in such a way that they tend to refrain from hospital visits. This
may may lead to depression and reduced quality of life, which may then impact on increases in
health care costs. The service provided by hospitals to these patients, is under-utilised by
the multi-ethnic people that make up the population. Through the researcher's previous
clinical experience, it was observed that patients were complaining of difficulty in getting
to the hospital, long waiting times, and also increasing transport costs. Thus, adoption of
self-care and early prevention has been suggested as a solution for the OA affected Malaysian
community. In addition, there is no home based exercise programme for patients with knee OA
in current health practice in Malaysia. Although some of these patients in Malaysia are
prescribed with home-based exercises, a fully comprehensive self-management programme is
lacking for patients generally. Therefore, there is a need for a home based self-management
exercise programme for people with knee OA which can be implemented in community setting
without frequent involvement of the hospitals. The UK Medical Research Council Guidance and
Framework on developing and evaluating complex interventions will be used to facilitate the
process of developing a complex intervention. A systematic review of the literature
identified an exercise programme called ESCAPE-Pain as the programme with the best evidence
for adaptation as a self-management programme to implement in Malaysia.
In phase 1, (already conducted), the investigators have undertaken interviews with patients
and healthcare professionals (HCPs) in Malaysia to identify their beliefs and attitudes
towards the ESCAPE-pain programme. Preliminary analysis reveals that patients with knee OA
and HCPs have positive views towards the implementation of the programme with integration of
a few new components.
In this phase, the investigators propose to undertake a feasibility randomised controlled
trial in which the investigators compare the modified ESCAPE-pain programme for the Malaysian
context, versus usual care in Malaysian OA patients. ESCAPE-pain is a rehabilitation
programme that helps people with osteoarthritis (OA) and/or chronic joint pain to self
-manage their condition. The programme aims to increase physical function and improve quality
of life. The ESCAPE-pain programme, will be run over six weeks, with participants attending
for one hour session, twice a week. Each session contains around a 20 minutes themed
discussion focused on helping to support self-management and followed by about 45 minutes of
exercise. The sessions will be led by the researcher who trained in how to deliver the
ESCAPE-pain programme.
This feasibility study is required to identify the best methods for a definitive trial in the
future, to test recruitment and other trial procedures, the acceptability of the intervention
and the way it is implemented and to provide insight into appropriateness of our outcome
measures, including providing data to permit estimation of effect size to be used in sample
size calculations for a definitive trial.
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