Sarah B. Garrett

发表

The Importance Of Integrating Narrative Into Health Care Decision Making.

Katharine A. Rendle, D. Dohan, Sarah B Garrett, 2016, Health affairs.

The promises of computational ethnography: Improving transparency, replicability, and validity for realist approaches to ethnographic analysis

Katharine A. Rendle, D. Dohan, K. Rendle, 2018 .

The Social Contexts of Birthing People with Public- and Private-Payer Prenatal Care: Illuminating an Understudied Aspect of the Patient Experience

Sarah B. Garrett, Melissa A. Simon, 2022, Health equity.

Foundations of the cultural repertoire: Education and social network effects among expectant mothers

Sarah B. Garrett, 2016 .

EngageUC: Developing an Efficient and Ethical Approach to Biobanking Research at the University of California

Arleen F. Brown, S. Dry, D. Dohan, 2015, Clinical and translational science.

Helping Teens Develop Healthy Social Skills and Relationships: What the Research Shows about Navigating Adolescence. American Teens. Child Trends Research Brief.

E. Hair, Justin Jager, Sarah B. Garrett, 2002 .

Antibias Efforts in United States Maternity Care: A Scoping Review of the Publicly Funded Health Equity Intervention Pipeline

Julie-Gai B Harris, Sarah B. Garrett, Melissa A. Simon, 2022, Clinical obstetrics and gynecology.

Background for Community-Level Work on Social Competency in Adolescence: Reviewing the Literature on Contributing Factors.

E. Hair, Justin Jager, Sarah B. Garrett, 2001 .

Developing neuropalliative care for sporadic Creutzfeldt-Jakob Disease

C. Ritchie, M. Geschwind, J. Gilissen, 2022, Prion.

Community recommendations on biobank governance: Results from a deliberative community engagement in California

Arleen F. Brown, S. Dry, B. Koenig, 2017, PloS one.

Beyond exploratory: a tailored framework for designing and assessing qualitative health research

D. Dohan, M. Halley, K. Rendle, 2019, BMJ Open.

Bearing Culture: Resources, Networks and the Transition to New Motherhood

Sarah B. Garrett, 2013 .

Goals of care conversations don't fit in a box': Hospice Staff Experiences and Perceptions of Advance Care Planning Quality Measurement.

C. Ritchie, R. Sudore, Gabrielle Dressler, 2020, Journal of pain and symptom management.

"It's Case by Case, and It's a Struggle": A Qualitative Study of Hospice Practices, Perspectives, and Ethical Dilemmas When Caring for Hospice Enrollees with Full-Code Status or Intensive Treatment Preferences.

C. Ritchie, R. Sudore, Krista L Harrison, 2020, Journal of palliative medicine.

Practices, challenges, and opportunities when addressing the palliative care needs of people living with dementia: Specialty memory care provider perspectives

C. Ritchie, Krista L Harrison, Sarah B Garrett, 2021, Alzheimer's & dementia.

Patient and clinician perspectives on a patient‐facing dashboard that visualizes patient reported outcomes in rheumatoid arthritis

J. Yazdany, G. Schmajuk, P. Katz, 2020, Health expectations : an international journal of public participation in health care and health policy.

Standard Versus Simplified Consent Materials for Biobank Participation: Differences in Patient Knowledge and Trial Accrual

J. Wiley, Marie Murphy, D. Dohan, 2017, Journal of empirical research on human research ethics : JERHRE.

The Continued Importance of Quality Parent–Adolescent Relationships During Late Adolescence

K. Moore, E. Hair, Sarah B Garrett, 2008 .

Hospice Staff Perspectives on Caring for People with Dementia: A Multisite, Multistakeholder Study.

C. Ritchie, R. Sudore, Krista L Harrison, 2020, Journal of palliative medicine.

Approaches to decision-making among late-stage melanoma patients: a multifactorial investigation

D. Dohan, K. Rendle, Corey M. Abramson, 2018, Supportive Care in Cancer.

Before Consent: Qualitative Analysis of Deliberations of Patients With Advanced Cancer About Early-Phase Clinical Trials.

Christopher J. Koenig, P. Munster, C. Daugherty, 2020, Journal of oncology practice.

"Captive by the Uncertainty"-Experiences with Anticipatory Guidance for People Living with Dementia and Their Caregivers at a Specialty Dementia Clinic.

C. Ritchie, J. Merrilees, Georges Naasan, 2022, Journal of Alzheimer's disease : JAD.

Parent-Teen Relationships and Interactions: Far More Positive Than Not. Child Trends Research Brief. Publication # 2004-25.

K. Moore, E. Hair, L. Lippman, 2004 .

"I Didn't Sign Up for This": Perspectives from Persons Living with Dementia and Care Partners on Challenges, Supports, and Opportunities to Add Geriatric Neuropalliative Care to Dementia Specialty Care.

Alexander K. Smith, Krista L Harrison, D. Dohan, 2022, Journal of Alzheimer's disease : JAD.

A Home-Based Care Research Agenda by and for Homebound Older Adults and Caregivers

B. Leff, C. Ritchie, Alexandria K. Mickler, 2021, Journal of applied gerontology : the official journal of the Southern Gerontological Society.

Unanticipated Therapeutic Value of the Patient-Centered Outcomes Research Institute (PCORI) Stakeholder Engagement Project for Homebound Older Adults.

B. Leff, C. Ritchie, Alexandria K. Mickler, 2020, Journal of the American Medical Directors Association.

Caregiver Experiences Navigating the Diagnostic Journey in a Rapidly Progressing Dementia

M. Geschwind, J. Gilissen, Sarah B. Garrett, 2022, Journal of geriatric psychiatry and neurology.

Program Implementation: What Do We Know?

K. Moore, Christina Theokas, Sarah B. Garrett, 2006 .

Community-Based Palliative Care Consultations: Comparing Dementia to Nondementia Serious Illnesses.

C. Ritchie, L. Hanson, Krista L Harrison, 2020, Journal of palliative medicine.

Interest in initiating an early phase clinical trial: results of a longitudinal study of advanced cancer patients

L. Trupin, J. Wiley, P. Munster, 2017, Psycho-oncology.

Unintended Consequences of Opioid Regulations in Older Adults with Multiple Chronic Conditions.

C. Ritchie, C. Miaskowski, Sarah B. Garrett, 2020, The Gerontologist.

Linking Broad Consent to Biobank Governance: Support From a Deliberative Public Engagement in California

B. Koenig, D. Dohan, Sarah B. Garrett, 2015, The American journal of bioethics : AJOB.

Characteristics of people with dementia lost to follow‐up from a dementia care center

C. Ritchie, Krista L Harrison, Sarah B Garrett, 2021, International journal of geriatric psychiatry.

Beyond Exploratory: A Tailored Framework for Assessing Rigor in Qualitative Health Services Research

D. Dohan, M. Halley, K. Rendle, 2017 .

Advance Directive and POLST Documentation in Decedents With Dementia at a Memory Care Center

C. Ritchie, Georges Naasan, Sarah B. Garrett, 2021, Neurology. Clinical practice.

Decision-making about clinical trial options among older patients with metastatic cancer who have exhausted standard therapies

D. Dohan, Sarah B Garrett, M. Tsang, 2020, Journal of geriatric oncology.

What advanced cancer patients with limited treatment options know about clinical research: a qualitative study

Christopher J. Koenig, L. Trupin, P. Munster, 2017, Supportive Care in Cancer.

Evaluation Measures Parent-Adolescent Relationship Scale

K. Moore, E. Michelsen, Sarah B Garrett, 2019 .

The Parent-Adolescent Relationship Scale

K. Moore, E. Hair, L. Lippman, 2005 .

Psychometric Analyses of the Parent-Adolescent Relationship Scale in the National Longitudinal Survey of Youth - 1997

K. Moore, E. Hair, E. Michelsen, 2003 .