Developing the evidence base of patient and public involvement in health and social care research: the case for measuring impact

This publication has 18 references indexed in Scilit:

• Quality and acceptability of patient-reported outcome measures used in chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME): a systematic review
  Quality of Life Research, 2011
• A model for developing outcome measures from the perspectives of mental health service users
  International Review of Psychiatry, 2011
• Can the impact of public involvement on research be evaluated? A mixed methods study
  Health Expectations, 2011
• A model and measure for quality service user involvement in health research
  International Journal of Consumer Studies, 2010
• Citizen and consumer involvement in UK public services
  International Journal of Consumer Studies, 2010
• Evaluation of Ankylosing Spondylitis Quality of Life (EASi-QoL): Reliability and Validity of a New Patient-reported Outcome Measure
  The Journal of Rheumatology, 2010
• Improving the evaluation of therapeutic interventions in multiple sclerosis: the role of new psychometric methods
  Health Technology Assessment, 2009
• The role of service user research in generating knowledge-based health and social care: from conflict to contribution
  Evidence & Policy, 2007
• Principles and indicators of successful consumer involvement in NHS research: Results of a Delphi study and subgroup analysis
  Health Policy, 2006
• Health technology assessment and its influence on health-care priority setting
  International Journal of Technology Assessment in Health Care, 2004