Collaborations et solutions en recherche sur le VIH, le VHC et les ITSS

Alberta

What do Alberta stakeholders view as the most important characteristics of community-based research?

On March 6, 2019, 23 community stakeholders gathered in Calgary to discuss community-based research (CBR) priorities and capacity-building needs in the province. Attendees included independent community leaders living with HIV, representatives from community-based organizations, researchers from Mount Royal University and the University of Calgary, and an Alberta Health Services employee.

To kick-off the meeting, attendees brainstormed what they viewed as the three most important characteristics of CBR. Attendees wrote down their ideas on sticky-notes and posted them on a flip chart, grouping their responses with similar ideas suggested by others. The image above is a word cloud generated from these groupings, where larger words indicate greater frequency than smaller words. Many stakeholders highlighted the importance of:

  • GIPA/MIPA
  • Engagement
  • Collaboration
  • Relationships
  • Equity
  • Addressing gaps in knowledge

These characteristics are consistent with the CBR Collaborative Centre’s ‘Principles of CBR’, which guide the initiatives undertaken by the centre and its regional teams. Hearing these principles echoed by Alberta stakeholders in the brainstorming activity served as a reminder to reflect on how we are supporting these ideas in our day-to-day work and in the Centre’s initiatives moving forward.

The March 6 consultation provided an opportunity to discuss many topics related to CBR in Alberta. Keep your eyes (and inboxes!) open for a full report on the consultation.

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Comment mesure-t-on le succès? Développer des outils de résultats partagés pour des services de logement supervisé en VIH dans l’Ouest du Canada

Une équipe multiprovinciale de l’Ouest canadien a utilisé une approche participative à l’évaluation de programme afin de développer des outils de résultats partagés pour des programmes de logement supervisé dans le secteur du VIH. L’équipe a développé ces outils pour démontrer qu’en plus d’améliorer la santé physique des personnes vivant avec le VIH, les programmes améliorent également leur qualité de vie.

Des outils de collecte de données initiales et de suivi ont été développés à l’aide d’une série d’ateliers participatifs, d’entrevues et de réunions avec des travailleurs des premières lignes, des clients et des membres de la famille de ces derniers. Ce processus avait pour objectif de concevoir collectivement des mesures des résultats qui seraient pratiques pour les utilisateurs de services et les travailleurs des premières lignes et qui pourraient démontrer l’évolution des clients au fil du temps.

Dirigé par Floyd Visser (The SHARP Foundation) et la Dre Cathy Worthington (Université de Victoria), ce projet a réuni des fournisseurs de services de tout l’Ouest canadien, y compris le Sanctum Group de Saskatoon, la McLaren Housing Society et la Dr. Peter AIDS Foundation de Vancouver. Les partenaires additionnels incluaient le Dr Brent Oliver (Université Mount Royal), le Dr Hart Krentz (Southern Alberta HIV/AIDS Clinic), Janice Duddy (Pacific AIDS Network) et un pair séropositif au VIH.

En plus de ces précieux outils, la nature collaborative du projet a rehaussé les relations entre les fournisseurs de l’Ouest du Canada. Ce projet leur a permis d’apprendre les uns des autres et de collaborer à renforcer les programmes de logement supervisé pour les personnes vivant avec le VIH.

Pour en savoir plus sur ce projet et sur d’autres initiatives du PRATICS 2.0, cliquez ici.

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New Implementation Science Research Design Tool

The Centre for Implementation Science at King’s College London has recently developed the ImpRes Tool. Its purpose is to support research teams who are in the process of designing implementation research and work to implement evidence-based interventions into practice.See: http://www.kingsimprovementscience.org/files/ImpRes_Guide_April_2018.pdf?utm_source=EIC+Stakeholders&utm_campaign=7c2e35f8b4-EMAIL_CAMPAIGN_2018_04_22&utm_medium=email&utm_term=0_ea81bd44fe-7c2e35f8b4-295895941

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MB HIV Collective Impact Network April Symposium Great Success!

A Great Success!
The Symposium was an overwhelming success with over 95 people in attendance on April13. The purpose of the event was for knowledge exchange, idea generation and for network building. We had people from Saskatchewan, Ontario, Nova Scotia as well as people from all over Manitoba!
We were pleased to have 18 posters including a quilt as a poster!
We particularly appreciated the many out-of-town presenters and participants who were able to attend.
Many thanks to all the helpers who made this happen: including volunteers, staff, students, & our Stewardship Team.
We will be preparing a report. Watch for it in our next Monthly e-news in June!

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S’orienter dans le nouveau paysage de financement de la recherche sur le VIH/VHC

L’ACRV a le plaisir d’annoncer qu’est maintenant commencée la période d’inscription à l’atelier pour les chercheurs sur le VIH en début ou en milieu de carrière, et le thème sera S’orienter dans le nouveau paysage de financement de la recherche sur le VIH/VHC. L’objet de l’atelier est de permettre aux chercheurs de réussir à se frayer un chemin dans les nouveaux programmes canadiens de financement de la recherche, de leur offrir des stratégies pour préparer et réussir des propositions de subvention et étudier les solutions de rechange en matière de financement de la recherche.

Cet atelier, qui sera coprésidé par les Drs Bob Hogg (Université Simon Fraser), Carol Strike (Université de Toronto) et Curtis Cooper (Université d’Ottawa), se tiendra en partenariat avec le Bureau de coordination de l’Alliance de recherche et de développement de l’Initiative canadienne de vaccin contre le VIH, la Société canadienne de santé internationale, les Instituts de recherche en santé du Canada et la Fondation canadienne de recherche sur le SIDA.

Les personnes qui souhaitent assister à cet atelier doivent faire parvenir leur candidature à l’Association canadienne de recherche sur le VIH. L’inscription est maintenant ouverte aux chercheurs sur le VIH/VHC de tous les volets de la recherche et qui satisfont aux critères suivants :

Les candidats doivent :

  • être citoyens canadiens ou immigrants reçus;
  • axer leur domaine de recherche sur le VIH ou la coinfection au VHC;
  • avoir une nomination professorale ou un poste de chercheur indépendant dans un hôpital ou autre organisme au moment de la présentation de la demande.

Il faut inclure dans la demande les renseignements suivants :

  • lettre de demande indiquant les motifs pour lesquels le candidat veut assister à l’atelier (200 mots au maximum);
  • une courte biographie de deux pages, au format NIH. Veuillez cliquer ici pour le lien.

Voici les détails de l’événement :

Date : Du dimanche 15 au mardi 17 janvier. Les séances se dérouleront du lundi matin au mardi soir.

Lieu : Buffalo Mountain Lodge, Banff (AB)

Coût : L’inscription à l’atelier est de 200 $. Cela comprend trois nuitées d’hébergement au Buffalo Mountain Lodge, tout le matériel de l’atelier et la nourriture pour toute la durée de la réunion. *À remarquer que les participants devront assumer leurs propres frais de déplacement aller et retour. *

Veuillez écrire un courriel à tmerkeepp@icid.com pour en savoir plus.

Inscrivez-vous maintenant! Date limite d’inscription : 21 Novembre

 

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Where are we now? The Impact of the IPV Protocol Screening Survey

Intimate partner violence (IPV) refers specifically to abuse within an intimate relationship, the immediate and long-term effects of which can have devastating impacts.

Recent studies are showing that people living with HIV experience a high burden of IPV, and although it has also been shown to be a significant risk factor in acquiring HIV, few studies have focused on how past or current experiences with IPV affect individual’s engagement to HIV care after their diagnosis.

The team at the Southern Alberta HIV Clinic in Calgary (SAC) believe in the importance of asking all individuals living with HIV a series of standardized questions, via the IPV Protocol Screening Survey, that address their experiences with IPV. The data collected from the last several years has allowed for a broader understanding of the prevalence of IPV in different and more diverse populations than previously reported, and has also led to the expansion of the definition of ‘communities impacted by IPV’ to include populations beyond those usually considered ‘vulnerable’.

The IPV Protocol Screening Survey is a low cost, high reward intervention that can positively impact individuals living with HIV and the effects of IPV and is accepted by both patients and providers because it gives space to acknowledge the impact of people’s experience with IPV and enhances HIV care outcomes while expressing empathy and understanding.

This project is ongoing and you can read more about their findings in the following articles:

Miller P, Siemieniuk RAC, Woodman K, Krentz HB, Gill MJ  Interpersonal violence and its impact on persons living with HIV: a social work response. Journal of HIV/AIDS & Social Services 2015; 14:308-318.

Rassi SE, Krentz HB, Siemieniuk RAC, Gill MJ Implementing an IPV screening protocol in HIV Care. AIDS Patient Care and STDs  2015; 29(3):1-9

Siemieniuk, RAC, Krentz HB, Gill MJ 2013 Intimate Partner Violence and HIV: A Review. Curr HIV/AIDS Reports 10:380-389. DOI 10.1007/s11904-013-0173-9

Siemieniuk, RAC, Krentz HB, Miller P, Woodman K, Gill MJ 2013 The clinical implications of high rates of intimate partner violence against HIV-positive women JAIDS 64(1):32-38

Siemieniuk, RAC, Miller P, Woodman K, Ko K, Krentz HB, Gill MJ 2012 Prevalence, clinical associations, and impact of intimate partner violence among HIV-infected gay and bisexual Men: a population based study. HIV Medicine   DOI:10.111/hiv 12005 (2012)

Siemieniuk RAC, Krentz HB, Gish JA, Gill MJ 2010. Domestic Violence Screening: Prevalence and Outcomes in a Canadian HIV Population. AIDS Patient Care and STDs 24(12):763-770.

 Questions or concerns about this project? Contact: hartmut.krentz@ahs.ca

 

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Calgary Men’s Wellness Initiative Survey

The Calgary Men’s Wellness Initiative is a community-based research project that investigates the health and wellness needs of the MSM population in Calgary. They have recently completed a survey and interviews that asked

  1. What are the health and wellness needs of gay, bisexual, queer and other men who have sex with men, including trans men?
  2. What gaps and barriers exist in the health sector for GBQM?

The results of this project are having a huge impact! There have been a number of educational outreach initiatives to inform service providers and community members. Findings have been shared in a community forum in Calgary, at a provincial meeting of HIV service providers, and at a one-day skills building conference for medical students and health care providers.  Additionally, The Calgary Sexual Health Centre has used the findings to inform an HIV/STI testing clinic twice a month. It has even sparked conversation about potentially developing an LGBTQ-specific health clinic in Calgary.

The data collected will also be used to guide a larger province-wide project that was recently funded by CIHR that aims to engage Alberta based researchers, decision makers, front line workers, and community-based organizations in identifying a provincial research agenda for HIV prevention in Alberta.

A summary report and other relevant publications are in the works and will be shared as soon as they’re available!

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Interpersonal violence and its impact on persons living with HIV: A social work response

The team at the Southern Alberta Clinic in Calgary has recently published an article entitled Interpersonal Violence and Its Impact on Persons Living with HIV: A Social Work Response. The article examines the significant burden of interpersonal violence among those living with HIV, as well as the key role that social workers play in service delivery around prevention, intervention, and education.

Follow this link to read the article in full.

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Where are we now? The Western Canada HIV Supported Housing Project

The Western Canada HIV Supported Housing: Outcome Tools Development Project (led by Dr. Cathy Worthington, University of Victoria and Floyd Visser, The SHARP Foundation) recognized a need for common outcome measures and outcome evaluation to support program delivery and sustain funding for HIV supported housing services, especially those services for people living with HIV/AIDS with complex needs. Housing is a key structural factor in HIV transmission and in determining the health of HIV; this study will create the foundation for outcome studies in participating HIV Supported Housing services.

Four agencies have been involved in the project: The SHARP Foundation (Calgary, AB), McLaren Housing Society (Vancouver, BC), Dr. Peter AIDS Foundation (Vancouver, BC), and Sanctum Housing (Saskatoon, SK). In March 2015, the project brought together stakeholders from the four HIV Supported Housing agencies, as well as individuals from public health, the homeless-serving sector, government, and academia at a two-day workshop. The project team discussed their needs for outcome measurements and established a plan to develop program-specific logic models to help inform the outcome measurement tool development process.

Over the summer, interviews will be conducted with service users and their family members at each of the four agencies to ensure that their perspectives on required outcome measures are included. The project team will meet in Fall 2015 to discuss their progress to date and to draft a common outcome measures tool. A database will be created and staff will be trained so that outcome measures can be collected and used for subsequent research.

This project will be instrumental in measuring the impact of HIV Supported Housing services on their clients and community and will help to leverage funding for these integral programs.

(Written by Kaylee Ramage)

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Where are we now? The impact of Intimate Partner Violence on HIV/AIDS disease care

Intimate Partner Violence (IPV) is a category of domestic abuse that refers specifically to abuse within an intimate relationship. It is a global health problem affecting millions of people every day. The relationship between HIV and IPV is complex not only because people affected by IPV more vulnerable to acquiring HIV, but the presence of IPV will impact individuals’ ability to access and maintain HIV care that may lead to poorer health outcomes. The presence of HIV infection may also increase the risk of subsequent IPV within a relationship.

The Southern Alberta Clinic in Calgary began researching IPV on individuals living with HIV in 2009 to determine the prevalence of IPV within their clinic population and how it impacts health outcomes. This involved implementing a universal screening survey that asked patients:

• if they were currently experiencing IPV,
• had experienced IPV in a past adult relationship,
• or had experienced abuse as a child.

Sociodemographic and clinical characteristics were compared between patients that reported IPV and those that did not. Comparisons of access and adherence to HIV care were also made between the two groups.

Over the past five years, almost 95% of the patients have been surveyed. Individuals currently experiencing IPV were immediately extracted from their situations; other patients who had previously dealt with IPV were referred to specialized caregivers with expertise in IPV. Last summer over 150 interviews were conducted to examine the acceptability of IPV screening in an HIV clinic setting. From these interviews a series of recommendations were made to help implement the screening survey in other HIV care centers. They hope to expand the program across the country to help improve the health of individuals living with HIV and IPV by encouraging other clinics to use the screening protocol on a routing basis.

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