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• Models of Care That Include Primary Care for Adult Survivors of Childhood Cancer

  Research Protocol

  November 12, 2020
• Care Interventions for People Living With Dementia and Their Caregivers

  Research Protocol

  July 25, 2019
• Can Physical Activity Improve the Health of Wheelchair Users? A Systematic Review

  Research Protocol

  April 12, 2019
• Diagnosis and Treatment of Clinical Alzheimer's-type Dementia (CATD)

  Research Protocol

  November 27, 2018
• Depression in Children: Systematic Review

  Research Protocol

  August 24, 2018
• Patient- or Participant-Generated Registries

  White Paper

  March 5, 2018
• Supporting Shared Decisions When Clinical Evidence Is Low (Session III)

  White Paper

  January 3, 2017
• EPC Methods: AHRQ End-User Perspectives of Rapid Reviews

  White Paper

  April 14, 2016
• Assessment Tools for Palliative Care

  Research Protocol

  April 14, 2016
• Barriers to Patient Engagement (Session II)

  White Paper

  September 30, 2015
• Patient Engagement: Roles of Activation, Evidence, and Context (Session I)

  White Paper

  September 30, 2015
• The Empirical Evidence of Bias in Trials Measuring Treatment Differences

  Research Report

  September 29, 2014
• Registries for Evaluating Patient Outcomes: A User’s Guide: 3rd Edition

  Research Report

  April 30, 2014
• Defining the Benefits of Stakeholder Engagement in Systematic Reviews

  White Paper

  March 18, 2014
• Information Technology Infrastructure for N-of-1 Trials (Chapter 5)

  Research Report

  February 12, 2014
• Global Health Evidence Evaluation Framework

  White Paper

  June 24, 2013
• The AHRQ Evidence-Based Care (EBC) Challenge

  Research Report

  June 1, 2013
• Identifying and Managing Nonfinancial Conflicts of Interest for Systematic Reviews

  Research Report

  May 23, 2013
• Public Deliberation To Elicit Input on Health Topics: Findings From a Literature Review

  Research Report

  February 1, 2013
• Addressing Tensions When Social/Family Support and Evidence-Based Care Collide (Session III)

  White Paper

  September 30, 2012
• Registry of Patient Registries (RoPR): Project Overview

  Research Report

  May 31, 2012
• Enhanced Functionality for the Distributed Research Network Pilot

  Research Report

  April 3, 2012
• Eliciting Patients’ Values and Preferences in Decision Making (Session II)

  White Paper

  September 30, 2011
• Communicating (Im)Precision and Uncertainty In Clinical Evidence (Session I)

  White Paper

  September 30, 2011
• Differing Levels of Clinical Evidence: Exploring Communication Challenges in Shared Decisionmaking

  Series Overview

  September 30, 2011
• Defining an Optimal Format for Presenting Research Needs

  Research Report

  June 10, 2011
• Engaging Stakeholders to Identify and Prioritize Topics for Future Research: Recommended activities and reporting practices

  Research Report

  June 10, 2011
• Realizing the Promise of Web 2.0: Addressing Health Disparities in Vulnerable Populations (Session III)

  White Paper

  September 30, 2010
• Realizing the Promise of Web 2.0: Engaging Community Intelligence (Session II)

  White Paper

  September 30, 2010
• Realizing the Promise of Web 2.0: Marketing and Dissemination of Patient-centered Health Research (Session I)

  White Paper

  September 30, 2010