Shannen Vallesi

Ms. Shannen Vallesi

university of western australia

Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 December 2017 in SSM - Population Health
Verified
Journal Article
Open access
LWLisa Wood
Lisa Wood
KMKaren Martin
Karen Martin
Hayley ChristianHayley Christian
Hayley Christian
SHSTEPHEN J HOUGHTON
STEPHEN J HOUGHTON
IKIchiro Kawachi
Ichiro Kawachi
SMSandra McCune
Sandra McCune
•Pet ownership is significantly associated with higher levels of social capital.•Social capital was associated with pet ownership in the U.S. and Australia.•Results are not confined to dog owners nor dog walkers.•Pets are an under-recognized conduit for building social capital.

Shannen VallesiShannen Vallesi
Shannen Vallesi
MTMatthew Tuson
Matthew Tuson
ADAndrew Davies
Andrew Davies
LWLisa Wood
Lisa Wood
Background: Although the poor health of people experiencing homelessness is increasingly recognised in health discourse, there is a dearth of research that has quantified the nature and magnitude of chronic health issues and morbidity among people experiencing homelessness, particularly in the Australian context. Methods: Analysis of the medical records of 2068 “active” patients registered with a specialist homeless health service in Perth, Western Australia as of 31 December 2019. Results: Overall, 67.8% of patients had at least one chronic physical health condition, 67.5% had at least one mental health condition, and 61.6% had at least one alcohol or other drug (AOD) use disorder. Nearly half (47.8%) had a dual diagnosis of mental health and AOD use issues, and over a third (38.1%) were tri-morbid (mental health, AOD and physical health condition). Three-quarters (74.9%) were multimorbid or had at least two long-term conditions (LTCs), and on average, each patient had 3.3 LTCs. Conclusions: The study findings have substantial implications from both a health risk and healthcare treatment perspective for people experiencing homeless. The pervasiveness of preventable health conditions among people experiencing homelessness also highlights the imperative to improve the accessibility of public health programs and screening to reduce their morbidity and premature mortality.

Shannen VallesiShannen Vallesi
Shannen Vallesi
LWLisa Wood
Lisa Wood
LDLyn Dimer
Lyn Dimer
MZMichelle Zada
Michelle Zada
Despite growing acknowledgement of the socially determined nature of health disparities among Aboriginal people, how to respond to this within health promotion programs can be challenging. The legacy of Australia’s assimilation policies have left profound consequences, including social marginalisation, limited educational opportunities, normalisation of premature death, and entrenched trauma. These social determinants, in conjunction with a reluctance to trust authorities, create barriers to accessing healthcare services for the prevention, treatment, and rehabilitation of chronic disease. The Heart Health program is a culturally sensitive cardiac rehabilitation program run at the local Aboriginal Medical Service in Perth, Western Australia that has since moved beyond cardiac education to provide a holistic approach to chronic disease management. A participatory action research framework was used to explore Heart Health participant and service provider perspectives on the barriers, enablers, and critical success factors to program participation and behaviour change. Thematic analysis of interview transcripts was undertaken, and through yarning (Aboriginal storytelling) sessions, many participants made unprompted reference to the impacts of white settlement, discrimination, and the forced fracturing of Aboriginal families, which have been explored in this paper reiterating the need for a social determinants lens to be taken when planning and implementing Aboriginal health promotion programs.

11 December 2018 in Housing, Care and Support
Verified
Journal Article
Closed access
LWLisa Wood
Lisa Wood
NWNicholas J.R. Wood
Nicholas J.R. Wood
Shannen VallesiShannen Vallesi
Shannen Vallesi
ASAmanda Stafford
Amanda Stafford
ADAndrew Davies
Andrew Davies
CCCraig Cumming
Craig Cumming
Purpose: Homelessness is a colossal issue, precipitated by a wide array of social determinants, and mirrored in substantial health disparities and a revolving hospital door. Connecting people to safe and secure housing needs to be part of the health system response. The paper aims to discuss these issues.Design/methodology/approach: This mixed-methods paper presents emerging findings from the collaboration between an inner city hospital, a specialist homeless medicine GP service and Western Australia’s inaugural Housing First collective impact project (50 Lives 50 Homes) in Perth. This paper draws on data from hospitals, homelessness community services and general practice.Findings: This collaboration has facilitated hospital identification and referral of vulnerable rough sleepers to the Housing First project, and connected those housed to a GP and after hours nursing support. For a cohort (n=44) housed now for at least 12 months, significant reductions in hospital use and associated costs were observed.Research limitations/implications: While the observed reductions in hospital use in the year following housing are based on a small cohort, this data and the case studies presented demonstrate the power of care coordinated across hospital and community in this complex cohort.Practical implications: This model of collaboration between a hospital and a Housing First project can not only improve discharge outcomes and re-admission in the shorter term, but can also contribute to ending homelessness which is itself, a social determinant of poor health.Originality/value: Coordinated care between hospitals and programmes to house people who are homeless can significantly reduce hospital use and healthcare costs, and provides hospitals with the opportunity to contribute to more systemic solutions to ending homelessness.

22 July 2016 in AHURI Final Report
Verified
Journal Article
Closed access
PDF file
LWLisa Wood
Lisa Wood
PFPaul Flatau
Paul Flatau
KZKaylene Zaretzky
Kaylene Zaretzky
SFSarah Foster
Sarah Foster
Shannen VallesiShannen Vallesi
Shannen Vallesi
DMDarja Miscenko
Darja Miscenko
This report finds that supporting formerly homeless people and those at risk of homelessness into public housing in Western Australia reduces their use of health services as well as the frequency with which they do so.

22 March 2019 in BMC Public Health
Verified
Journal Article
Open access
PDF file
Shannen VallesiShannen Vallesi
Shannen Vallesi
PFPaul Flatau
Paul Flatau
MTMonica Thielking
Monica Thielking
JMJessica L. Mackelprang
Jessica L. Mackelprang
KTKathryn M. Taylor
Kathryn M. Taylor
RCRyan Courtney
Ryan Courtney
Chronic homelessness is a problem characterised by longstanding inability to attain or maintain secure accommodation. Longitudinal research with homeless populations is challenging, and randomised controlled trials that evaluate the effectiveness of intensive, case management interventions aimed at improving housing and health-related outcomes for chronically homelessness people are scant. More research is needed to inform programmatic design and policy frameworks in this area. This study protocol details an evaluation of the Journey to Social Inclusion – Phase 2 program, an intervention designed to reduce homelessness and improve outcomes in chronically homeless adults. J2SI Phase 2 is a three-year, mixed methods, multi-site, RCT that enrolled 186 participants aged 25 to 50 years between 07 January 2016 and 30 September 2016 in Melbourne. The intervention group (n = 90 recruited) receives the J2SI Phase 2 program, a trauma-informed intervention that integrates intensive case management and service coordination; transition to housing and support to sustain tenancy; and support to build social connections, obtain employment and foster independence. The comparison group (n = 96 recruited) receives standard service provision. Prior to randomisation, participants completed a baseline survey. Follow-up surveys will be completed every six months for three years (six in total). In addition to self-report data on history of homelessness and housing, physical and mental health, substance use, quality of life, social connectedness and public service utilisation, linked administrative data on participants’ public services utilisation (e.g., hospitalisation, justice system) will be obtained for the three-year period pre- and post-randomisation. Semi-structured, qualitative interviews will be conducted with a randomly selected subset of participants and service providers at three time-points to explore changes in key outcome variables and to examine individual experiences with the intervention and standard service provision. An economic evaluation of the intervention and associated costs will also be undertaken. Results of this trial will provide robust evidence on the effectiveness of J2SI Phase 2 compared to standard service provision. If the intervention demonstrates effectiveness in improving housing, health, quality-of-life, and other social outcomes, it may be considered for broader national and international dissemination to improve outcomes among chronically homeless adults. Australian New Zealand Clinical Trials Registry ACTRN12616000162415 (retrospectively registered 10-February-2016).