Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 8 de 8
Filtrar
1.
Psychiatry Res ; 284: 112641, 2020 02.
Artículo en Inglés | MEDLINE | ID: mdl-31757641

RESUMEN

Stigmatizing attitudes among primary care (PC) providers potentially contribute to poor health outcomes for individuals with serious mental illness (SMI). In this pilot study, our primary aim is to test the feasibility, and preliminary implementation of two interventions (contact and education) to help change provider attitudes and behavior. Participants were 39 primary care providers from two Veterans Affairs medical centers with 19 randomized to the contact intervention and 20 to the education intervention. Both interventions were delivered in a group setting face-to-face. Stigmatizing attitudes were measured using Opening Minds Scale for Health Care Providers, Attribution Questionnaire and Social Distance Scale at baseline, one month and three months. Data were analyzed using repeated measures analysis of variance (ANOVA). Most providers were white, female, nurses, and older than age 50. For each of the three measures of stigmatizing attitudes there was no statistically significant treatment-by-time interaction rejecting our hypothesis that contact intervention will result in significantly greater reduction in stigmatizing attitudes. Qualitative analysis suggests that the contact intervention was perceived as much needed. This study informs future research to reduce provider stigma. Our intervention was modeled on interventions designed for the general public; different interventions may be needed for providers.


Asunto(s)
Actitud del Personal de Salud , Personal de Salud/psicología , Trastornos Mentales/psicología , Atención Primaria de Salud/métodos , Estereotipo , Adulto , Estudios de Factibilidad , Femenino , Humanos , Masculino , Trastornos Mentales/terapia , Persona de Mediana Edad , Proyectos Piloto , Distancia Psicológica , Estigma Social , Encuestas y Cuestionarios
2.
Psychiatry Res ; 273: 578-585, 2019 03.
Artículo en Inglés | MEDLINE | ID: mdl-30716597

RESUMEN

Native Hawaiians and other Pacific Islanders (NHPI) rarely seek mental health treatment for reasons that are minimally understood. To assess the mental illness stigma context in NHPI communities that may be contributing to low help-seeking, this study collected novel stigma data from two large U.S. NHPI communities from October 2017 to January 2018, then compared this data to national stigma data from the U.S. public. Survey data were collected from 222 community-dwelling NHPI participants recruited by research-trained NHPI staff. Surveys incorporated well-established vignettes describing persons with major depression and schizophrenia. Study data were compared to U.S. general public data from the 2006 General Social Survey: the largest U.S. stigma study. Compared to the U.S. public, NHPI participants reported greater stigma toward mental illness in ways likely to impede help-seeking including: (1) more frequently endorsing stigmatizing causal attributions of depression and schizophrenia, (2) less frequently perceiving disorders as serious, and (3) more commonly desiring social distance from persons with depression. Study data are the first to reveal the presence of a strongly stigmatizing context in NHPI communities likely to hinder NHPI help-seeking. Thus, culturally tailoring anti-stigma interventions to appropriately target NHPI mental health attitudes and beliefs may prove effective in promoting NHPI help-seeking.


Asunto(s)
Trastornos Mentales/etnología , Trastornos Mentales/psicología , Nativos de Hawái y Otras Islas del Pacífico/etnología , Nativos de Hawái y Otras Islas del Pacífico/psicología , Estigma Social , Adulto , Femenino , Hawaii/etnología , Humanos , Masculino , Trastornos Mentales/terapia , Persona de Mediana Edad , Islas del Pacífico/etnología , Distancia Psicológica , Percepción Social , Encuestas y Cuestionarios
3.
Obstet Gynecol ; 131(5): 850-855, 2018 05.
Artículo en Inglés | MEDLINE | ID: mdl-29630024

RESUMEN

OBJECTIVE: To evaluate the implementation of pharmacist-prescribed hormonal contraceptives in California after a recent expansion of pharmacists' scope of practice. METHODS: A probability sample of 480 licensed California retail pharmacies (stratified by nonrural or rural location and independent or chain status) was included in a cross-sectional "secret shopper" telephone survey assessing the availability of pharmacist-prescribed hormonal contraceptives and service details. Survey data were analyzed using weighted descriptive statistics, CIs, and Wald tests. RESULTS: Findings included data from 457 pharmacies (response rate 95.2%). Only 5.1% of pharmacies reported providing pharmacist-prescribed hormonal contraceptives (95% CI 2.9-7.2%). This proportion did not differ significantly between rural and nonrural pharmacies (P=.83) nor between independent and chain pharmacies (P=.40). Five of the 22 pharmacies that were providing pharmacist-prescribed hormonal contraceptives informed secret shoppers that all allowed hormonal methods were available; most of these pharmacies (77.3%) did proactively describe that a health history was required before receiving medications. Only half of pharmacies providing pharmacist-prescribed hormonal contraceptives would do so for minors although this was allowed by law. CONCLUSION: In the first year after statewide protocol implementation, only a small proportion of retail pharmacies across California has begun offering hormonal contraception services. In the absence of additional supportive legislation regarding reimbursement for pharmacist services, increases in scope of practice regulations to build a larger network of contraceptive providers may not be effective in increasing access to birth control.


Asunto(s)
Servicios Comunitarios de Farmacia/estadística & datos numéricos , Anticonceptivos Hormonales Orales/uso terapéutico , Accesibilidad a los Servicios de Salud/estadística & datos numéricos , California/epidemiología , Anticoncepción/métodos , Anticoncepción/estadística & datos numéricos , Estudios Transversales , Prescripciones de Medicamentos/estadística & datos numéricos , Femenino , Humanos , Farmacia/métodos , Farmacia/estadística & datos numéricos
4.
Obesity (Silver Spring) ; 25(12): 2128-2136, 2017 12.
Artículo en Inglés | MEDLINE | ID: mdl-29071803

RESUMEN

OBJECTIVE: This study examined the state of obesity, diabetes, and associated health disparities among understudied multiracial, Native Hawaiian and Other Pacific Islander (NHOPI), and American Indian and Alaskan Native (AIAN) adults. METHODS: Aggregated data for 184,617 adults from the California Health Interview Survey (2005 to 2011) were analyzed to determine obesity, diabetes, poor/fair health, and physical disability prevalence by racial group. Logistic regressions controlling for age, gender, and key social determinants (education, marital status, poverty, health insurance) generated multiracial, NHOPI, and AIAN adults' odds ratios (ORs) for our targeted health conditions versus non-Hispanic white adults. RESULTS: Obesity, diabetes, and other targeted health conditions were highly prevalent among multiracial, NHOPI, and AIAN adults, who displayed significantly greater adjusted odds than non-Hispanic white adults for obesity (ORs = 1.2-1.9), diabetes (ORs = 1.6-2.4), poor/fair health (ORs = 1.4-1.7), and, with the exception of NHOPI adults, physical disability (ORs = 1.5-1.6). Multiracial and AIAN adults with obesity also had significantly higher adjusted odds of diabetes (OR = 1.5-2.6) than non-Hispanic white adults with obesity. CONCLUSIONS: Multiracial, NHOPI, and AIAN adults experience striking obesity-related disparities versus non-Hispanic white adults, urging further disparities research with these vulnerable minority populations.


Asunto(s)
Disparidades en Atención de Salud/normas , Obesidad/etnología , Obesidad/epidemiología , Adulto , Etnicidad , Femenino , Encuestas Epidemiológicas , Humanos , Indígenas Norteamericanos , Masculino , Persona de Mediana Edad , Nativos de Hawái y Otras Islas del Pacífico , Obesidad/patología
5.
Psychiatr Serv ; 68(6): 573-578, 2017 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-28142389

RESUMEN

OBJECTIVE: Rural African Americans are disproportionately affected by social stressors that place them at risk of developing psychiatric disorders. This study aimed to understand mental health, mental health treatment, and barriers to treatment from the perspective of rural African-American residents and other stakeholders in order to devise culturally acceptable treatment approaches. METHODS: Seven focus groups (N=50) were conducted with four stakeholder groups: primary care providers, faith community representatives, college students and administrators, and individuals living with mental illness. A semistructured interview guide was used to elicit perspectives on mental health, mental health treatment, and ways to improve mental health in rural African-American communities. Inductive analysis was used to identify emergent themes and develop a conceptual model grounded in the textual data. RESULTS: Stressful living environments (for example, impoverished communities) and broader community-held beliefs (for example, religious beliefs and stigma) had an impact on perceptions of mental health and contributed to barriers to help seeking. Participants identified community-level strategies to improve emotional wellness in rural African-American communities, such as providing social support, improving mental health literacy, and promoting emotional wellness. CONCLUSIONS: Rural African Americans experience several barriers that impede treatment use. Strategies that include conceptualizing mental illness as a normal reaction to stressful living environments, the use of community-based mental health services, and provision of mental health education to the general public may improve use of services in this population.


Asunto(s)
Negro o Afroamericano/psicología , Necesidades y Demandas de Servicios de Salud , Disparidades en el Estado de Salud , Trastornos Mentales/terapia , Población Rural , Adolescente , Adulto , Arkansas , Femenino , Grupos Focales , Humanos , Entrevistas como Asunto , Masculino , Salud Mental , Persona de Mediana Edad , Pobreza , Investigación Cualitativa , Estigma Social , Apoyo Social , Adulto Joven
6.
Psychiatr Serv ; 66(3): 265-71, 2015 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-25727114

RESUMEN

OBJECTIVE: The aim of this study was to test whether gender moderates intervention effects in the Coordinated Anxiety Learning and Management (CALM) intervention, a 12-month, randomized controlled trial of a collaborative care intervention for anxiety disorders (panic disorder, generalized anxiety disorder, posttraumatic stress disorder, and social anxiety disorder) in 17 primary care clinics in California, Washington, and Arkansas. METHODS: Participants (N=1,004) completed measures of symptoms (Brief Symptom Inventory [BSI]) and functioning (mental and physical health components of the 12-Item Short Form [MCS and PCS] and Healthy Days, Restricted Activity Days Scale) at baseline, six, 12, and 18 months. Data on dose, engagement, and beliefs about psychotherapy were collected for patients in the collaborative care group. RESULTS: Gender moderated the relationship between treatment and its outcome on the BSI, MCS, and Healthy Days measures but not on the PCS. Women who received collaborative care showed clinical improvements on the BSI, MHC, and Healthy Days that were significantly different from outcomes for women in usual care. There were no differences for men in collaborative care compared with usual care on any measures. In the intervention group, women compared with men attended more sessions of psychotherapy, completed more modules of therapy, expressed more commitment, and viewed psychotherapy as more helpful. CONCLUSIONS: These findings contribute to the broader literature on treatment heterogeneity, in particular the influence of gender, and may inform personalized care for people seeking anxiety treatment in primary care settings.


Asunto(s)
Trastornos de Ansiedad/terapia , Conducta Cooperativa , Atención Primaria de Salud/métodos , Evaluación de Programas y Proyectos de Salud/métodos , Adolescente , Adulto , Anciano , Arkansas , California , Femenino , Estudios de Seguimiento , Humanos , Masculino , Persona de Mediana Edad , Grupo de Atención al Paciente , Evaluación de Programas y Proyectos de Salud/estadística & datos numéricos , Factores Sexuales , Resultado del Tratamiento , Washingtón , Adulto Joven
7.
Adm Policy Ment Health ; 42(5): 588-92, 2015 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-25217100

RESUMEN

Integrating two distinct and complementary paradigms, science and engineering, may produce more effective outcomes for the implementation of evidence-based practices in health care settings. Science formalizes and tests innovations, whereas engineering customizes and optimizes how the innovation is applied tailoring to accommodate local conditions. Together they may accelerate the creation of an evidence-based healthcare system that works effectively in specific health care settings. We give examples of applying engineering methods for better quality, more efficient, and safer implementation of clinical practices, medical devices, and health services systems. A specific example was applying systems engineering design that orchestrated people, process, data, decision-making, and communication through a technology application to implement evidence-based depression care among low-income patients with diabetes. We recommend that leading journals recognize the fundamental role of engineering in implementation research, to improve understanding of design elements that create a better fit between program elements and local context.


Asunto(s)
Ingeniería , Práctica Clínica Basada en la Evidencia , Investigación sobre Servicios de Salud , Ciencia , Integración de Sistemas , Humanos , Gestión del Conocimiento
8.
J Consult Clin Psychol ; 71(1): 53-61, 2003 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-12602425

RESUMEN

Recent estimates of mental health morbidity among adults reporting same-gender sexual partners suggest that lesbians, gay men, and bisexual individuals may experience excess risk for some mental disorders as compared with heterosexual individuals. However, sexual orientation has not been measured directly. Using data from a nationally representative survey of 2,917 midlife adults, the authors examined possible sexual orientation-related differences in morbidity, distress, and mental health services use. Results indicate that gay-bisexual men evidenced higher prevalence of depression, panic attacks, and psychological distress than heterosexual men. Lesbian-bisexual women showed greater prevalence of generalized anxiety disorder than heterosexual women. Services use was more frequent among those of minority sexual orientation. Findings support the existence of sexual orientation differences in patterns of morbidity and treatment use.


Asunto(s)
Bisexualidad/psicología , Homosexualidad Femenina/psicología , Homosexualidad Masculina/psicología , Trastornos Mentales/epidemiología , Servicios de Salud Mental/estadística & datos numéricos , Adulto , Anciano , Depresión/diagnóstico , Depresión/epidemiología , Manual Diagnóstico y Estadístico de los Trastornos Mentales , Femenino , Humanos , Masculino , Trastornos Mentales/diagnóstico , Persona de Mediana Edad , Prevalencia , Encuestas y Cuestionarios , Estados Unidos/epidemiología
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA
...