Patient Advocacy
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Subject Areas on Research
- A Summary of the 2020 Gastric Cancer Summit at Stanford University.
- A Systematic Review of Patient- and Family-Level Inhaled Corticosteroid Adherence Interventions in Black/African Americans.
- ALS clinical research learning institutes (ALS-CRLI): empowering people with ALS to be research ambassadors.
- Advocacy skills training for young adult cancer survivors: the Young Adult Survivors Conference at Camp Māk-a-Dream.
- Agency is messy: get used to it.
- American Heart Association and nonprofit advocacy: past, present, and future. A policy recommendation from the American Heart Association.
- An Evidence Map for Interventions Addressing Transition from Pediatric to Adult Care: A Systematic Review of Systematic Reviews.
- Applications of therapeutic jurisprudence in rehabilitation for people with severe and disabling mental illness.
- Benefits and drawbacks to hormone replacement therapy among nursing home patients.
- Best practices for mental health in child welfare: parent support and youth empowerment guidelines.
- Bioethicists' statement on the U.S. Supreme Court's Cruzan decision.
- Choosing Wisely in Adult Hospital Medicine: Co-creation of New Recommendations for Improved Healthcare Value by Clinicians and Patient Advocates.
- Concealed medicines for people with schizophrenia: a U.S. perspective.
- Consumer protection and the HMO backlash: are HMOs to blame for drive-through deliveries?
- Cultural carrying capacity: Organ donation advocacy, discursive framing, and social media engagement.
- Desegregation of hospitals and medical societies in North Carolina.
- Do patients want access to their medical records?
- Does bedside rationing violate patients' best interests? An exploration of "moral hazard".
- Effect of an advocacy intervention on mental health in Chinese women survivors of intimate partner violence: A randomized controlled trial
- Effective Partnering in Conducting Benefit-Risk Patient Preference Studies: Perspectives From a Patient Advocacy Organization, a Pharmaceutical Company, and Academic Stated-Preference Researchers.
- Eligibility and Radiologic Assessment in Adjuvant Clinical Trials in Bladder Cancer.
- Engaging Patient Advocates and Other Stakeholders to Design Measures of Patient-Centered Communication in Cancer Care.
- Family representative payeeship and violence risk in severe mental illness.
- Genetic privacy needs a more nuanced approach.
- How Surrogate Decision-Makers for Patients With Chronic Critical Illness Perceive and Carry Out Their Role.
- Ignorance is bliss but not in health care: teaching consumers about quality care.
- Image Gently: progress and challenges in CT education and advocacy.
- Impacts of managed care patient protection laws on health services utilization and patient satisfaction with care.
- In Support of a Patient-Driven Initiative and Petition to Lower the High Price of Cancer Drugs.
- Integrative tumor board: recurrent breast cancer or new primary? UCSF Osher Center for Integrative Medicine and UCSF Carol Franc Buck Breast Care Center.
- Lying for patients: physician deception of third-party payers.
- Lying to insurance companies: the desire to deceive among physicians and the public.
- Making a difference in the health care of veterans: 9 things you should know.
- Managed care organizations should not disclose their physicians' financial incentives.
- Managed care: rationing without justice, but not unjustly.
- Medical futility decisions and physicians' legal defensiveness: the impact of anticipated conflict on thresholds for end-of-life treatment.
- Models for delivering survivorship care.
- Monitoring versus interim analysis of clinical trials: a perspective from the pharmaceutical industry.
- Nurse Knowledge and Engagement in Health Policy Making: Findings From a Pilot Study.
- Nurse leaders can shape ethical cultures.
- Nursing advocacy in North Carolina.
- Obesity and managed care: a role for activism and advocacy?
- Patients who want their family and physician to make resuscitation decisions for them: observations from SUPPORT and HELP. Study to Understand Prognoses and Preferences for Outcomes and Risks of Treatment. Hospitalized Elderly Longitudinal Project.
- Patients' rights.
- Patients, physicians, and clinical trials: the other side of the coins.
- Physicians' experiences with prehospital do-not-resuscitate orders in North Carolina.
- Placental-blood transplantation.
- Public policy and obesity: the need to marry science with advocacy.
- Report condemns NHS complaints procedure.
- Research and advocacy in nutrition therapy: our specialty needs you.
- S.1232: A Late Entry in the Race for Malpractice Reform
- Safety-promoting behaviors of community-dwelling abused Chinese women after an advocacy intervention: A randomized controlled trial
- Science and recovery in schizophrenia.
- Statistical controversies in clinical research: data access and sharing-can we be more transparent about clinical research? Let's do what's right for patients.
- Surrogates' perceptions about feeding tube placement decisions.
- Telephone intervention to improve the mental health of community-dwelling women abused by their intimate partners: a randomised controlled trial.
- The Future Role of the United States in Global Health: Emphasis on Cardiovascular Disease.
- The Unrealized Potential of Malpractice Arbitration
- The evolution of advocacy and orthopaedic surgery.
- The experience of care partners of patients with Parkinson's disease psychosis.
- Trust in Managed Care Organizations
- Using central IRBs for multicenter clinical trials in the United States.
- Using the PRACTICE mnemonic to apply cultural competency to genetics in medical education and patient care.
- Violations of human rights: health practitioners as witnesses.
- Voices of Oncology Nursing Society members matter in advocacy and decisions related to U.S. Health Policy
- What constitutes a psychiatric emergency: clinical and legal dimensions.