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Do enhanced general practice services improve health outcomes and health service use? Flinders QUality Enhanced general practice Services Trial (Flinders - QUEST)

Do enhanced general practice services improve health outcomes and health service use? Flinders QUality Enhanced general practice Services Trial (Flinders - QUEST)

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12617001589370
Acronym
Flinders QUEST
Enrollment
1044
Registered
2017-11-28
Start date
2018-04-30
Completion date
2018-09-28
Last updated
2023-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The Australian health care system is facing many challenges as a result of an ageing population, rising rates of chronic and complex disease and a strong demand from consumers for more and higher quality health care services. A high performing and adequately resourced primary health care sector is needed to address these challenges and produce better population health outcomes and sustainable health care funding into the future. Flinders QUEST will test whether Australian general practices that are assisted (logistically and financially) to deliver enhanced services can produce better patient health outcomes and improved health service use.

Interventions

General practices (located in Adelaide, South Australia) in the intervention arm will deliver enhanced services to trial participants for a 12 month period. The enhanced services will be provided by the participant's usual general practice clinical team. Practices however will be supported (both financially and logistically) to deliver the enhanced services. The logistical support will include administrative assistance for participant recruitment and the provision of a Practice Facilitator who w

General practices (located in Adelaide, South Australia) in the intervention arm will deliver enhanced services to trial participants for a 12 month period. The enhanced services will be provided by the participant's usual general practice clinical team. Practices however will be supported (both financially and logistically) to deliver the enhanced services. The logistical support will include administrative assistance for participant recruitment and the provision of a Practice Facilitator who will support practices to incorporate the intervention elements into routine systems of care. The enhanced general practice services to be provided are as follows: (1) Enrollment with a preferred GP Intervention arm practices will record the trial participant’s preferred GP in clinical (comments field) and appointment (notes field) practice systems. This will flag to practice staff (the clinical and administrative teams) that the patient is enrolled in the trial and has a preferred GP. Participants enrolled in the Intervention arm will be provided a folder comprising trial written materials (Care Plan, future appointments and referrals). Participants will be asked to inform practice staff of their participation in the trial (and preferred GP) when making appointments. (2) Longer GP appointments GP Medicare funded appointments are time based: Level A: “Brief consultations”; Level B: “Standard consultations” (<20 minutes); Level C “Long consultations” (>20 minutes) and Level D “Prolonged Consultations” (>40 minutes). Longer appointments will be defined as Level C and D consultations. A facilitator will assist practices to make changes to practice appointment systems to accommodate longer consultations for trial participants. Each practice will decide what changes will be necessary to allow this and the best manner in which to implement the changes. (3) Follow-up after significant health events (Emergency Department presentation or hospital admission) Intervention arm participants will be contacted by clinical practice staff for practice or home based review within seven days of the participant experiencing a significant health event, where this is clinically indicated. (4) Same day appointments for children and young people experiencing acute conditions The participation of children and young people in the Intervention arm of the trial will be recorded in the clinical (comments field) and appointment (notes field) practice systems. This will flag to all practice staff (the clinical and administrative teams) that the child or young people should receive priority access to same day appointments if they (or their parents) contact the practice seeking an appointment for an acute condition.

Sponsors

Flinders University of South Australia
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Healthy volunteers
No

Inclusion criteria

Participants will have been assessed by their GPs as having high health care needs and possibly likely to benefit from enhanced services. Participants will be drawn from three cohorts: (1) Children and young people (under 18 years of age), (2) Elderly (65 years of age or over) people or (3) Adults (18 to 64 years of age) with two or more chronic diseases.

Exclusion criteria

A clinically dominant disease likely to shorten life expectancy Unable to comprehend English Suffer from significant cognitive impairment Severe mental illness Not community dwelling Enrolled in another health intervention study Enrolled in a chronic disease management program.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 12, 2026