Health Care While Homeless: Barriers, Facilitators, and the Lived Experiences of Homeless Individuals Accessing Health Care in a Canadian Regional Municipality.
Adult
Canada
Continuity of Patient Care
/ organization & administration
Empathy
Female
Financing, Personal
/ economics
Health Services Accessibility
/ organization & administration
Ill-Housed Persons
/ psychology
Humans
Interviews as Topic
Male
Middle Aged
Patient-Centered Care
/ organization & administration
Primary Health Care
/ organization & administration
Professional-Patient Relations
Qualitative Research
Transportation
/ economics
Trust
Vulnerable Populations
Canada
barriers
facilitators
health-seeking behavior
qualitative descriptive
qualitative’ semi-structured interviews
thematic analysis
transformative framework
Journal
Qualitative health research
ISSN: 1049-7323
Titre abrégé: Qual Health Res
Pays: United States
ID NLM: 9202144
Informations de publication
Date de publication:
11 2019
11 2019
Historique:
pubmed:
28
2
2019
medline:
12
5
2020
entrez:
28
2
2019
Statut:
ppublish
Résumé
Persons struggling with housing remain significantly disadvantaged when considering access to health care. Effective advocacy for their needs will require understanding the factors which impact their health care, and which of those most concern patients themselves. A qualitative descriptive study through the lens of a transformative framework was used to identify barriers and facilitators to accessing health care as perceived by people experiencing homelessness in the regional municipality of Niagara, Canada. In-person, semi-structured interviews with 16 participants were completed, and inductive thematic analysis identified nine barriers and eight facilitators. Barriers included affordability, challenges finding primary care, inadequacy of the psychiatric model, inappropriate management, lack of trust in health care providers, poor therapeutic relationships, systemic issues, and transportation and accessibility. Facilitators included accessibility of services, community health care outreach, positive relationships, and shelters coordinating health care. Knowledge of the direct experiences of marginalized individuals can help create new health policies and enhance the provision of clinical care.
Identifiants
pubmed: 30810072
doi: 10.1177/1049732319829434
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng