Implementing work-related Mental health guidelines in general PRacticE (IMPRovE): a protocol for a hybrid III parallel cluster randomised controlled trial

Implementation Science

Duncan Mortimer¹  Michael Kidd²  Danielle Mazza³  Samantha Chakraborty³  Vera Camões-Costa³  Alex Collie⁴  Joanne Enticott⁵  Bianca Brijnath⁶  Sharon Reid⁷  Lyndal Trevena⁷  Justin Kenardy⁸ 

[1] Centre for Health Economics, Monash Business School, Monash University, Melbourne, Australia;College of Health and Medicine, The Australian National University, Canberra, Australia;Department of General Practice, Monash University, Melbourne, Australia;Insurance Work and Health Group, Monash University, Melbourne, Australia;Monash Centre for Health Research and Implementation, Monash University, Melbourne, Australia;National Ageing Research Institute, Parkville, Australia;School of Allied Health, Curtin University, Perth, Australia;Sydney School of Public Health, Faculty of Medicine and Health, The University of Sydney, Camperdown, Australia;University of Queensland, Brisbane, Australia;

关键词: Guideline implementation;    General practice;    Hybrid III trial;    Mental health;    Work;    Integrated Knowledge Translation;   

DOI  :  10.1186/s13012-021-01146-8

来源: Springer

【 摘 要 】

BackgroundThe Clinical Guideline for the Diagnosis and Management of Work-related Mental Health Conditions in General Practice (the Guideline) was published in 2019. The objective of this trial is to implement the Guideline in general practice.Trial designImplementing work-related Mental health conditions in general PRacticE is a hybrid III, parallel cluster randomised controlled trial undertaken in Australia. Its primary aim is to assess the effectiveness of a complex intervention on the implementation of the Guideline in general practice. Secondary aims are to assess patient health and work outcomes, to evaluate the cost-effectiveness of the trial, and to develop a plan for sustainability.MethodsA total of 86 GP clusters will be randomly allocated either to the intervention arm, where they will receive a complex intervention comprising academic detailing, enrolment in a community of practice and resources, or to the control arm, where they will not receive the intervention. GP guideline concordance will be assessed at baseline and 9 months using virtual simulated patient scenarios. Patients who meet the eligibility criteria (>18years, employed, and receiving care from a participating GP for a suspected or confirmed work-related mental health condition) will be invited to complete surveys about their health and work participation and provide access to their health service use data. Data on health service use and work participation compensation claim data will be combined with measures of guideline concordance and patient outcomes to inform an economic evaluation. A realist evaluation will be conducted to inform the development of a plan for sustainability.ResultsWe anticipate that GPs who receive the intervention will have higher guideline concordance than GPs in the control group. We also anticipate that higher concordance will translate to better health and return-to-work outcomes for patients, as well as cost-savings to society.ConclusionsThe trial builds on a body of work defining the role of GPs in compensable injury, exploring their concerns, and developing evidence-based guidelines to address them. Implementation of these guidelines has the potential to deliver improvements in GP care, patient health, and return-to-work outcomes.Trial registrationACTRN12620001163998, November 2020

【 授权许可】

CC BY