Skip to content

Evaluation of Lived Experience Peer Support Intervention for Mental Health Service Consumers in Primary Care

Evaluation of Lived Experience Peer Support Intervention for Mental Health Service Consumers in Primary Care

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12623001189617
Acronym
PS-PC
Enrollment
2
Registered
2023-11-17
Start date
2023-11-09
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

None listed

Brief summary

Peer Workers have lived experience of mental ill-health and are intentionally employed to support individuals with mental ill-health as well as their family and carers. These Peer Workers are inaccessible to many in need, especially for those whose main or only support is through general practice. Our aim is to trial the implementation of a co-designed lived experience peer support intervention for mental health consumers in primary care.

Interventions

One-to-one peer support for mental healthcare consumers in primary care, delivered by lived experience peer workers. Depending on the needs of the individual, peer workers often provide support similar to an informal carer while using their personal experience and knowledge. however they also use their personal experience and knowledge in their support. They can provide information, a listening ear, company, and act as an advocate on the individual's behalf. Few resources are involved beyond the

One-to-one peer support for mental healthcare consumers in primary care, delivered by lived experience peer workers. Depending on the needs of the individual, peer workers often provide support similar to an informal carer while using their personal experience and knowledge. however they also use their personal experience and knowledge in their support. They can provide information, a listening ear, company, and act as an advocate on the individual's behalf. Few resources are involved beyond the tools that peer workers use in the usual course of their employment (e.g., laptop computer, mobile phone etc.). All participants will have access to 12 hours of support over a period three to four months, Some might use all 12 hours in the first month. Others might spread their time out across the given period (i.e., weekly or twice weekly). There is no set interval and this will vary based on preferences/needs. Face-to-face consultation will be prioritised. However, because the clinics are rural while the Community Managed Organisations (CMOs) are not, some flexibility is expected. Where it is not possible for a peer worker to travel to the participant, telehealth (videocalling) will be used. (For example, if a participant requests an immediate or next-day appointment.) Clinics will provide quiet consult rooms and make technology available to participants to ensure they have access. Monitoring of adherence will be conducted through the peer worker. Where participants are not attending appointments (beyond the norm), the peer worker will contact their peer coordinator. There will also be constant communication between the project officer, peer worker coordinator, and practice staff to monitor adherence. Adherence will be monitored alongside potential for adverse events.

Sponsors

Prof Sharon Lawn
Lead SponsorIndividual

Study design

Allocation
Non-randomised trial
Primary purpose
Educational / counselling / training

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

A consumer is eligible to participate if they are 18 years of age or older, have a diagnosis of a mental health condition (or present with symptoms indicating the likelihood of a mental health condition), attend participating practices, willing to give informed consent to participate in the study and not already receiving peer support through an alternative funded programme will be eligibile for participation.

Exclusion criteria

A consumer will be excluded if they have a significant mental or physical illness likely to disrupt capacity to participate in the trial (as measured by GP assessment of current suicidality risk and/or K10 cut of score of >40/50). Consumers who are unable to speak English and those unable to provide informed consent will also be excluded.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 8, 2026