RACGP GP Research Project Noticeboard

This project aims to understand how the current Therapeutic Guideline on medical abortion can be improved to support GPs to safely and confidently provide medical abortion to their patients. We will interview GPs and GPs-in-training to understand their use of the current Guideline and seek their views on how it could be improved to support use at the point-of-care. We will use these findings to develop a set of specific recommendations to apply to the Therapeutic Guideline on medical abortion.

Geographic location the project wishes to recruit from: Australia-wide

Link to website:

Investigators: Chief Investigator Dr Sonia Srinivasan, SPHERE Centre of Research Excellence, Monash University sonia.j.srinivasan@gmail.com

GP investigator: Dr Sonia Srinivasan

Contact person and details: Dr Karen Nolidin karen.nolidin@monash.edu

Brief Description of participants or practices: AHPRA-registered GPs or GP registrars who have familiarity with use of Therapeutic Guidelines (on any topic).

Commencement date of the project: 23/06/2025

Closing date for recruitment: 23/09/2025

Link to survey:

Time involvement of participants: 60 minute interview

Compensation offered: $200 gift voucher

We are conducting research on Prescriber behaviours in relation to oral retinoids and contraception. This study aims to explore the potential gaps in the current models of care that may result in inadequate contraception amongst women taking oral retinoids.

Brief Description of participants or practices: We are seeking Dermatologists, General Practitioners and Pharmacists who are involved in the prescribing and/or counselling of oral retinoids. Participation is open to individuals who practice anywhere in Australia

Time involvement of participants: 20-30min interview or 45min focus group - Flexible scheduling

Compensation offered: $100 gift card to say thank you

GP investigator: Dr Ka-Kiu Cheung

Evidence of approval by a Human Research Ethics Committee: GU Ref No: 2025/349

Link to survey:
 

Measuring what Matters to Australian Mothers () e-Delphi Round 1 survey is now live.  

The aim of the MMAMs project is to develop, pilot and evaluate patient-reported experience measures (PREMs) and patient-reported outcome measures (PROMs) that best measure the experiences and outcomes recognised as most important by those giving birth.  

You may choose to participate in one, two or all three of the surveys. The first survey is expected to take about 30 minutes to complete. We plan to close the first survey on Sunday 20^th July 2025. 

This project will deliver the first consumer co-designed maternity PREMs and PROMs tools in the world. With real-world impact, the mission of this project is to enable health system improvements to deliver safe and quality maternity care that meet the needs and values of the near 300,000 people giving birth every year in Australia. 

Link to survey:

Geographic location the project wishes to recruit from: Australia-wide

Investigators: A/Prof Zoe Bradfield at Curtin University (lead)

Time: 30 minutes

Commencement date of the project: 20 June 2025

Closing date for recruitment: 30 November 2025

Link to website:

GP investigator: Dr. Ka-Kiu (KK) Cheung

Contact: Project Manager, Dr Lauren Spark, lauren.spark@curtin.edu.au

Ethics approval: Curtin University Human Research Ethics Committee (HREC) has approved this study (HRE2025-0200). 

Western Sydney Sexual Health Centre and the University of Sydney are seeking to better understand General Practitioner (GP) knowledge, attitudes and practices regarding ordering HSV serology. Internationally, guidelines differ in their recommendations in this area and clinical practice may vary accordingly. Your responses will greatly assist us in facilitating GP education and training opportunities and in working with partnering organisations in the sexual health sector to improve genital herpes case management and patient education.

Link to survey:

Time involvement of participants: 10 minutes

CPD points: Reviewing Performance

Contact person and details: Dr Nicholas Comninos at Western Sydney Sexual Health Centre: nicholas.comninos@health.nsw.gov.a / Tel: 02 98433124

Commencement date of the project: 16/06/2025

This project has received an RACGP ������Ƶ Research Grant to look at the effect of part time training on AGPT registrars. This part of the study is a qualitative semistructured interview study with new fellows of the AGPT program that have previously trained part time. p

Geographic location the project wishes to recruit from: Australia-wide

Investigators: Dr Jenna Lyttle, FRACGP, Senior Lecturer in Clinical Medicine, Deakin University Dr Talia Follett, FRACGP, Senior Local Medical Officer for the RACGP Prof Gary Rogers, Dean of Medicine, Deakin University Prof Steve Trumble, General Practice and Curriculum Workforce, Deakin University Prof Parker Magin, Senior Research Unit Academic Advisor and ReCEnT Chief Investigator, RACGP Dr Angelo D'Amore, Research Manager, RACGP

GP investigator: Dr Jenna Lyttle & Dr Talia Follett

Compensation offered: $150 gift card

Contact person and details: Dr Jenna Lyttle E-mail: Jenna.Lyttle@deakin.edu.au or Dr Talia Follett E-mail: Talia.Follett@racgp.org.au

Brief Description of participants or practices: GP's Australia wide who have fellowed in the last 5 years & who completed at least 75% of their training part time.

Commencement date of the project: 4/04/2025

Closing date for recruitment: 15/12/2025

Time involvement of participants: Semi- structured interviews of 45-60 mins duration, either in person, on zoom or on the phone

The James Lind Alliance Priority Setting Partnership will identify the pressing unanswered research questions for the sepsis care in Australia. The JLA PSP method consist of the following: 1. A lead in survey (Survey 1), An interim Survey (Survey 2), 3. The PSP Workshop

Geographic location the project wishes to recruit from: Australia-wide

Investigators: Prof Andrew Udy Prof Simon Finfer Prof Naomi Hammond Prof Yugeesh Lankadeva Dr Stephen Macdonald A/Prof Kimberley Haines Dr Manoj Saxena Dr Paul Secombe Dr Alex Poole

GP investigator: Dr Li Wan

Link to website:

Contact person and details: Rose Messiha E-mail: rose.messiha@monash.edu

Brief Description of participants or practices: GPs having had experience with sepsis

Commencement date of the project: 27/05/2025

Closing date for recruitment: 30/08/2025

Link to survey:

Time involvement of participants: 10 min to complete survey

Recent European guidelines have changed to recommend universal first trimester CMV screening to identify maternal infection early and facilitate timely antenatal interventions to reduce congenital infection. We are asking GPs to complete a 10-minute survey to evaluate whether routine CMV screening in pregnancy would be acceptable and feasible to implement if Australia were to introduce routine antenatal CMV screening. The study findings will help inform future health policy in antenatal care.

Investigators: Project Supervisor PROF Lisa Hui Other Investigators A/Prof Ines Rio (GP), DR Tanya Tripathi, DR Natalia Rode (GP), Ms. Kath Swinburn, A/Prof Hayley Smithers-Sheedy

Link to website:

Brief Description of participants or practices: GPs currently practising in Australia who have seen pregnant patients any time in the last 5 years.

Geographic location the project wishes to recruit from: Australia-wide

Compensation offered: Option to go into a draw to win one of 3 $100 gift cards

Commencement date of the project: 4/06/2025

Link to survey:

Time involvement of participants: 10 minutes

GP investigator: Dr Natalia Rode; A/Prof Ines Rio

Contact person and details: Natalia Rode natalia.rode@unimelb.edu.au

Closing date for recruitment: 30/06/2025

The BREATHE study is an MRFF-funded trial improving early detection of chronic breathlessness in general practice. Patients complete a short digital screening tool via mobile phone, and the results are sent to the GP’s eMR. 50% of practices will additionally receive decision support prompts. The study is low-burden, integrates into usual care, and aims to improve timely diagnosis and management of conditions like COPD, asthma, and heart failure.

Geographic location the project wishes to recruit from: : Australia-wide but based in NSW

Investigators: Joint CIA Professor Christine Jenkins, CI Professor Ben Freedman, CI Dr Anthony Paulo Sunjaya, and AI Dr Nicole Lowres

GP investigator: Joint CIA Professor Charlotte Hespe, CI Dr Katrina Giskes, CI Dr Andrew Kiight, CI Dr John Fardy, CI A/Professor Ralph Audehm, AI Dr Ai-vee Chua, AI Dr Michael Tam, AI Dr Michael Wright, AI Dr Christopher Pearce, and AI Dr Kerry Hancock

Contact details: Professor Charlotte Hespe charlotte.hespe@nd.edu.au GP Clinician, Glebe Family Medical Practice Head of GP and Primary Care Research UNDA Sydney School of Medicine

Brief Description of participants sought: Participating general practices must use the Best Practice electronic medical record system and have a patient population exceeding 1000 active individuals. Eligible patients are those aged 18 years or older who are scheduled to see a GP. Patients with physical or intellectual disabilities that prevent them from completing the self-screening questionnaire independently will be excluded from participation.

Commencement date of the project: 22/05/2025

Closing date for recruitment: 31/12/2025

Time involvement of participants: The study runs for 12 months. GPs attend a 15-minute training session, review digital screening results during usual consultations, and conduct brief follow-ups (3, 6, 12 months) for ~10 patients. Practice staff attend 30-minute training and support admin tasks like updating logs, coordinating follow-ups, de-identifying documents, and mailing forms (~1–2 hrs/month). The workflow integrates easily into routine practice.

Compensation offered: Practice Remuneration Participating practices will receive financial compensation to acknowledge the staff time and administrative support required to participate in the study. The amount varies depending on the study arm to which the practice is randomised: Up to AUD $5,000 for practices in the BREATHE SMART arm Up to AUD $9,500 for practices in the BREATHE SMART + CDSS arm This remuneration covers activities such as IT setup, baseline data extraction, and patient recruitment.

If CPD hours applicable, the CPD type (Measuring outcomes, Reviewing performance, ������Ƶal activities): GP participants will qualify for CPD in all 3 areas - Measuring outcomes, Reviewing performance, educational activities. We will provide certificates of participation including your time taken to do the activities.

Clinical trial registration, if applicable: BREATHE SMART has been registered on the Australian and New Zealand Clinical Trial Registry ACTRN12624001451594 BREATHE CDSS has been registered on the Australian and New Zealand Clinical Trial Registry ACTRN12624001455550

The  is a research project led by investigators based at the Department of General Practice and Primary Care, and the Doherty Institute, University of Melbourne, and the Kirby Institute, University of New South Wales. It is funded by The Department of Health and Aged Care via the APPRISE network.

The OUTPOST study will establish the first primary care-based Australian prospective cohort study of individuals with acute COVID-19/Influenza/RSV infection followed-up to 48 weeks for any persistent health symptoms. The overarching aim of OUTPOST is to estimate the 12-week point prevalence of Long COVID/Flu/RSV compared to noninfected controls and the disease burden up to 48 weeks post infection.

OUTPOST is linked to primary care from the outset to match the requirement of the funder of improving the detection and management of Long COVID at the level of general practices. This is because most patients with acute respiratory infections are likely to seek care from their GPs.

OUTPOST plans to recruit 1500 participants with acute COVID/Flu/RSV and 500 non-infected participants Australia-wide over an 18-month period. The study started accrual in August 2024. It is expected that up to 150 infected individuals (10%) may develop persistent symptoms consistent with Long COVID or the equivalent after Flu/RSV at 12-weeks versus 5% in the non-infected group (N=25). Each participant is reimbursed up to $110 for completing surveys at baseline, 6-weeks, 12-weeks, 24weeks and 48-weeks.

Throughout the study period, participating general practices are supported by a dedicated state-based study coordinator. Practices receive an incentive payment in recognition of their time and contribution.

In addition to recruitment through general practices, participants are also being recruited via pharmacies located near the participating practices, as well as through a nationwide social media campaign.

Geographic location the project wishes to recruit from (State, or Australia-wide):
Australia- wide

Investigators:
Prof Lena Sanci, Prof Andrew Lloyd, Prof Jon Emery, A/Prof Jo-Anne Manski-Nankervis, A/Prof Patty Chondros, Dr Miranda Smith, Prof Douglas Boyle, Ms Maria Stambas, Dr Ruby Biezen, A/Prof. Lucette Cysique, Mrs Hayley Ivanusic, Ms Oonagh Macken

GP investigator:
Lena Sanci | Head / Professor MBBS., PhD., FRACGP
Department of General Practice and Primary Care | Melbourne Medical School
Faculty of Medicine, Dentistry & Health Sciences
MP: (+61) 0429417504
P: (61) +3 8344 9010 E: l.sanci@unimelb.edu.au

Contact person and details (Name, email address, etc):
Ruby Biezen BSc, MAppSc, PhD
Senior Research Fellow - Lead, Infectious Disease Surveillance and Stewardship in Primary Care
Department of General Practice and Primary Care | Melbourne Medical School
Faculty of Medicine, Dentistry & Health Science
The University of Melbourne
W: +61 3 9035 4886| M: +61 417 149 974
E: ruby.biezen@unimelb.edu.au
F: +61 3 9347 6136 | W:

Brief Description of participants or practices (inclusion/exclusion criteria, or a hyperlink to this):

The study aims to recruit participants who have experienced acute respiratory symptoms within the past 7 days. However, participants do not need to be symptomatic at the time of registration.

Participants invited through general practice must meet the following criteria:

Active patients, as defined by RACGP standards
12 years of age or older
Have a mobile phone number recorded in their file

Time involvement of participants:
Enrolled participants will be asked to complete online surveys at five time points over almost a year: baseline (week 0), week 6, week 12, week 24, and week 48. Each survey is estimated to take 30–40 minutes to complete.

Compensation offered:
Eligible participants receive a free TOUCH Bio RAT kit.
Enrolled participants receive $20 or $30 gift vouchers upon completion of each survey. In total, they may receive up to $110 in gift vouchers for completing the entire study.

Commencement date of the project:
1/08/2024

Closing date for recruitment:
31/12/2025

Link to survey:

Link to website:

Note:
Please share this opportunity with your colleagues and patients.
The study aims to recruit participants who have experienced acute respiratory symptoms within the past 7 days. However, participants do not need to be symptomatic at the time of registration or eligibility screening.
Eligible participants may choose to receive a TOUCH Bio RAT kit either by express post or by collecting it from a local participating clinic or pharmacy, as listed on the study website.
Participants who test positive for Flu A/B, RSV, or COVID-19 may enrol in the study.
Asymptomatic participants may register in advance and retain the TOUCH Bio RAT kit for future use if they develop symptoms. Alternatively, they may be recruited into the control group of the study through age and gender-matching if they remain asymptomatic.

This Australia-wide project aims to improve care for adults with traumatic brain injury (TBI) with a focus on people in rural/remote regions, Culturally & Linguistically Diverse & Aboriginal & Torres Strait Islander Communities. It is funded by the MRFF Mission for TBI & led by Prof Jennie Ponsford AO. We invite GPs to participate in a brief survey about practices and needs in care of individuals & their family members following TBI. This will inform training programs & resource development.

Geographic location the project wishes to recruit from: Australia-wide

Investigators: Prof Jennie Ponsford, Dr Jessica Trevena-Peters, Dr. Cynthia Honan, Prof. Leanne Togher, Assoc. Prof. Dana Wong, Prof. Jennifer Fleming, Prof. Tamara Ownsworth, Assoc. Prof. Grahame Simpson, Emer. Prof. Jacinta Douglas, Dr Zoe Adey-Wakeling, Dr Clare Ramsden, Assoc. Prof. Rene Stolwyk, Dr. Travis Wearne, Dr. Bruce Powell, Nick Rushworth, Dr. Ann Livingstone, Dr. Marina Downing, Janet Wagland, Dr. Dean McKenzie, Miffy Durham

GP investigator: Dr Mukesh Haikerwal AC

Contact person and details: Study Email: tbi.rehabproject@monash.edu OR DR JESSICA TREVENA-PETERS School of Psychological Sciences Monash University E: jessica.trevena-peters@monash.edu

Brief Description of participants or practices (inclusion/exclusion criteria): All General Practitioners across Australia are invited to participate (it does not matter how in/frequently they see adults with a traumatic brain injury and/or their family members for care). We are inviting all General Practitioners across Australia to participate in a 5-10 minute online survey about care following Traumatic Brain Injury and share the survey with their colleagues.

Commencement date of the project: 28/03/2025

Closing date for recruitment: 29/08/2025

Link to survey:

Link to website:

Time involvement of participants: 5-10 minutes

Evaluate if a lifestyle-focused text message program can improve breast cancer survivors’ outcomes and be beneficial for patients and GPs. Feedback from >500 patients found a similar program useful and motivating but wanted it from their GP. Trial setup is easy and fast (~1-hour). Your team will: 1. Search for eligible patients (no data leaves the practice) 2. Send 1 text message with a link to the study information sheet and e-consent

Compensation offered: $200 per practice and CPD hours (details on website)

Geographic location the project wishes to recruit from: Australia-wide

Investigators: Prof Julie Redfern - Bond University Dr Anna Singleton - University of Sydney (GP) A/Prof Carolyn Ee - Western Sydney University/Flinders University Dr Stephanie Partridge- University of Sydney Prof Raymond Chan - Flinders University Dr Kirsty Stuart - University of Sydney A/Prof Elisabeth Elder - University of Sydney Dr Nashid Hafiz - University of Sydney Dr Karice Hyun - University of Sydney A/Prof Jennifer McIntosh – University of Melbourne

GP investigator: A/Prof Carolyn Ee - Western Sydney University/Flinders University

Practices sought: any practice that can search for eligible patients and send 1 text message using the system of your choice. The process is faster and easier if your practice has PenCAT.

Patients sought: people who finished active breast cancer treatment (surgery and/or chemotherapy and/or radiation therapy) within the past 3 years and attended at least 1 GP appointment in the past 2 years.

Link to website:

Contact person and details: Dr Anna Singleton (anna.singleton@sydney.edu.au)

Time involvement of participants: Patients: 2-years. The patients receive a 6-month lifestyle-focused text message program at the start or end of the trial, which provides evidence-based tips for managing health and weblinks to free resources and services. Patients also fill in short surveys (5-10mins) every 6-months for 2-years. Practice: 2-years. However, the University of Sydney team manages the patients’ participation (no additional work for your practice).

If CPD hours applicable, the CPD type: Measuring Outcomes, Reviewing Performance and ������Ƶal Activities CPD hours are available over the 2-3 years that your practice is involved. GPs can self-claim CPD hours. We provide a guide for maximum and minimum hours, but these are flexible, and GPs can self-judge.

Commencement date of the project: 28/04/2023

Closing date for recruitment: 31/12/2026

We're very keen to collaborate! Please reach out to me if you have any questions (anna.singleton@sydney.edu.au).

Our published trial protocol is here:

Our study compares two ways of prescribing an opioid medicine for people with back pain, either normal care, or including other pain relief options in addition to the opioid. We are not sure which way works best for the patient. This study involves a cluster randomised controlled trial, using medication use and pain as outcomes. You are invited to participate in this study as a general practitioner who treats people in the community presenting with back pain.

Geographic location the project wishes to recruit from: Australia-wide

Investigators: Dr Christina Abdel Shaheed, Professor Chris Maher, Professor Andrew McLachlan, Professor Fiona Blyth, Associate Professor Patrick Kelly, Associate Professor Fiona Stanaway, Dr Rachel Thompson, Philip Clare (The University of Sydney) Professor Louisa Degenhardt, Dr Thomas Lung (UNSW) Professor Rowena Ivers (UOW)

Contact details: Dr. Christina Abdel Shaheed Institute for Musculoskeletal Health. Level 10, North King George V Building, Royal Prince Alfred Hospital (C39) T: 02 8627 6236 christina.abdelshaheed@sydney.edu.au

Inclusion: Participating practices must be eligible to prescribe opioids. You are asked to screen and enrol between 12-15 eligible participants who have presented to you with low back pain where opioids are appropriate.

The patient cannot:
Have contra-indications to opioid medicines, be less than 18 years of age, being for cancer or receiving palliative treatment. The patient must be a holder of an Australian Medicare card (see PIS for full exclusions)

Commencement date of the project: 21/11/2024

Closing date for recruitment: 4/10/2025

Time involvement of participants: For GPs, this includes time to undertake 30-60 minute training package, 6 monthly practice visit, and approximately half an hour for each patient recruited.

Compensation offered: $1000 for GP for each patient recruited

Availability of CPD points: Self logging

Clinical trial registration: ACTRN12622001505796

Sciatica is a debilitating condition. The DREAM trial is a randomised, superiority, parallel-group, placebo-controlled, triple-blinded trial investigating the efficacy and safety of duloxetine in participants with chronic sciatica of at least 3 months duration and will include patients seen in general practices, specialist outpatient clinics, hospital emergency departments or from hospital in-patient wards.

Geographic location the project wishes to recruit from: Australia-wide

Investigators: Doctor Giovanni Ferreira, Professor Christopher Maher, Professor Christine Lin (University of Sydney), Professor Laurent Billot The George Institute for Global Health, Professor Richard Day (UNSW), Professor Rowena Ivers UOW (GP), Professor Martin Underwood Warwick University, UK, Professor Andrew McLachlan University of Sydney (Sydney School of Pharmacy), Doctor Bethan Richards Royal Prince Alfred Hospital, Professor Nanna Finnerup Aarhus University, Denmark

Contact details: dream_trial@sydney.edu.au. Level 10N, King George V Building Royal Prince Alfred Hospital (C39) PO Box M179, Missenden Road NSW 2050 AUSTRALIA T: +61 2 8627 6447

Inclusions criteria: Adults (18 years old and above) with radiating pain into one leg in a dermatomal distribution, for at least 3 months of moderate intensity pain, an adequate understanding of English

Exclusion criteria: Known or suspected specific pathologies in the spine, malignancy, spinal surgery or other interventional procedure in the preceding 6 months/ scheduled, pregnant, breastfeeding. (see PIS for full exclusions list)

Commencement date of the project: 21/11/2024

Closing date for recruitment: 30/06/2027

Time involvement of participants: Baseline survey, 10-minute survey will completed online or by phone 6 times over the next year (at week 4, 8, 12, 16, 26 and 52). Daily SMS asking participants to record a pain score, time to take study medication for up to 14 weeks.

Compensation offered: Study participants receive the study medication free of charge. Participants receive gift voucher/s of up to $150 in total over the 1-year study period after reaching certain trial milestones.

Availability of CPD points: Self logging