Stakeholder Participation

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  Subject Areas on Research

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