Stakeholder Participation
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Subject Areas on Research
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A Multilevel Approach to Stakeholder Engagement in the Formulation of a Clinical Data Research Network.
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Advancing Value-Based Models for Heart Failure: A Call to Action From the Value in Healthcare Initiative's Value-Based Models Learning Collaborative.
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An evaluation of stakeholder engagement in comparative effectiveness research: lessons learned from SWOG S1415CD.
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Application of the RAND-UCLA Appropriateness Methodology to a Large Multidisciplinary Stakeholder Group Evaluating the Validity and Feasibility of Patient-Centered Standards in Geriatric Surgery.
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Applied Rapid Qualitative Analysis to Develop a Contextually Appropriate Intervention and Increase the Likelihood of Uptake.
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Be good, communicate, and collaborate: a qualitative analysis of stakeholder perspectives on adding a chiropractor to the multidisciplinary rehabilitation team.
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Brief Report: A Survey of Autism Research Priorities Across a Diverse Community of Stakeholders.
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Building capacity for advances in tuberculosis research; proceedings of the third RePORT international meeting.
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Challenges With Engaging Military Stakeholders for Clinical Research at the Point of Care in the U.S. Military Health System.
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Chronic disease stigma, skepticism of the health system, and socio-economic fragility: Qualitative assessment of factors impacting receptiveness to group medical visits and microfinance for non-communicable disease care in rural Kenya.
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Clinical trials recruitment planning: A proposed framework from the Clinical Trials Transformation Initiative.
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Community and Stakeholder Engagement.
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Consensus on Language for Advance Informed Consent in Health Care-Associated Pneumonia Clinical Trials Using a Delphi Process.
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Developing Treatment Guidelines During a Pandemic Health Crisis: Lessons Learned From COVID-19.
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Developing a Primary Care-Focused Intervention to Engage Patients With Osteoarthritis in Physical Activity: A Stakeholder Engagement Qualitative Study.
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Developing an Inclusive and Welcoming LGBTQ Clinic.
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Development of a Prospective Real-World Data Clinical Registry of Children and Adolescents With Migraine.
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Ethics of DNA research on human remains: five globally applicable guidelines.
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Guideline-Directed Medical Therapy Clinics: A Call to Action for the Heart Failure Team.
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Hospital Standards to Promote Optimal Surgical Care of the Older Adult: A Report From the Coalition for Quality in Geriatric Surgery.
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Human-centered design as a guide to intervention planning for non-communicable diseases: the BIGPIC study from Western Kenya.
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Identifying Priorities to Improve the System of Care for Children With Complex Health Needs in North Carolina: Process and Outcomes of Systematic Stakeholder Engagement.
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Implementing core outcomes in kidney disease: report of the Standardized Outcomes in Nephrology (SONG) implementation workshop.
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Importance of Participant-Centricity and Trust for a Sustainable Medical Information Commons
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Improving Cardiovascular Drug and Device Development and Evidence Through Patient-Centered Research and Clinical Trials: A Call to Action From the Value in Healthcare Initiative's Partnering With Regulators Learning Collaborative.
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Integrating Stakeholder Engagement With Claims-Based Research on Health Insurance Design and Bipolar Disorder.
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Leveraging Patient Preference Information in Medical Device Clinical Trial Design.
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Medicaid and CHIP Child Health Beneficiary Incentives: Program Landscape and Stakeholder Insights.
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Performance Measures Based on How Adults With Cancer Feel and Function: Stakeholder Recommendations and Feasibility Testing in Six Cancer Centers.
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Politically Correct Heart Failure Research in America to Avoid Geographic Variation.
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Providing early detection and early intervention for autism spectrum disorder in South Africa: stakeholder perspectives from the Western Cape province.
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Qualitative Exploration of Engaging Patients as Advisors in a Program of Evidence Synthesis: Cobuilding the Science to Enhance Impact.
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Quality indicators assessing antibiotic use in the outpatient setting: a systematic review followed by an international multidisciplinary consensus procedure.
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Quality indicators for responsible antibiotic use in the inpatient setting: a systematic review followed by an international multidisciplinary consensus procedure.
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Recommendations to Enhance Pediatric Cardiovascular Drug Development: Report of a Multi-Stakeholder Think Tank.
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Researchers, Patients, and Stakeholders Evaluating Comparative-Effectiveness Research: A Mixed-Methods Study of the PCORI Reviewer Experience.
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Stakeholder Engagement in Pragmatic Clinical Trials: Emphasizing Relationships to Improve Pain Management Delivery and Outcomes.
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Stakeholder perspectives on large-scale marine protected areas.
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Standardizing, harmonizing, and protecting data collection to broaden the impact of COVID-19 research: the rapid acceleration of diagnostics-underserved populations (RADx-UP) initiative.
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Strategies for Effective Stakeholder Engagement in Strengthening Referral Networks for Management of Hypertension Across Health Systems in Kenya.
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Streamlining and Reimagining Prior Authorization Under Value-Based Contracts: A Call to Action From the Value in Healthcare Initiative's Prior Authorization Learning Collaborative.
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The Elephant in the Room: Too Much Medicine in Musculoskeletal Practice.
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The Impact of COVID-19 on Patient, Family Member, and Stakeholder Research Engagement: Insights from the PREPARE NOW Study.
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Toward Accelerated Authorization and Access to New Medicines for Juvenile Idiopathic Arthritis.
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Transparent sharing of digital health data: A call to action.
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Unique Review Criteria and Patient and Stakeholder Reviewers: Analysis of PCORI's Approach to Research Funding.
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Use of a human-centered design approach to adapt a nurse-led cardiovascular disease prevention intervention in HIV clinics.
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Wake-up call from Hong Kong.
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Who Will Drive the Change? Democratizing Health Data.