User’s Guide to Implementing Patient-Reported Outcomes Assessment in Clinical Practice
暂无分享,去创建一个
Thomas E. Elliott | Joanne Greenhalgh | Rachel Hess | Bryce B. Reeve | Joanne Greenhalgh | Neil K. Aaronson | Maria J. Santana | Michele Y. Halyard | Rachel Hess | Deborah M. Miller | Claire F. Snyder | B. Reeve | N. Aaronson | C. Snyder | R. Hess | M. Santana | J. Greenhalgh | M. Halyard | T. E. Elliott
[1] A Bowling,et al. Short Form 36 (SF-36) Health Survey questionnaire: which normative data should be used? Comparisons between the norms provided by the Omnibus Survey in Britain, the Health Survey for England and the Oxford Healthy Life Survey. , 1999, Journal of public health medicine.
[2] J. Greenhalgh. The applications of PROs in clinical practice: what are they, do they work, and why? , 2009, Quality of Life Research.
[3] D. Berwick. The science of improvement. , 2008, JAMA.
[4] T. Cook,et al. Quasi-experimentation: Design & analysis issues for field settings , 1979 .
[5] David Feeny,et al. Framework to assess the effects of using patient-reported outcome measures in chronic care management , 2014, Quality of Life Research.
[6] L E Kazis,et al. Health status reports in the care of patients with rheumatoid arthritis. , 1990, Journal of clinical epidemiology.
[7] Brian R Ott,et al. Patient versus informant perspectives of Quality of Life in Mild Cognitive Impairment and Alzheimer's disease , 2004, International journal of geriatric psychiatry.
[8] Ron D Hays,et al. Comparison of Mail and Telephone in Assessing Patient Experiences in Receiving Care from Medical Group Practices , 2005, Evaluation & the health professions.
[9] M B Callahan,et al. Using quality of life measurement to enhance interdisciplinary collaboration. , 2001, Advances in renal replacement therapy.
[10] Jon Nicholl,et al. Testing survey methodology to measure patients' experiences and views of the emergency and urgent care system: telephone versus postal survey , 2010, BMC medical research methodology.
[11] David Cella,et al. Assessment is not enough: a randomized controlled trial of the effects of HRQL assessment on quality of life and satisfaction in oncology clinical practice , 2007, Psycho-oncology.
[12] Karon F. Cook,et al. Mode effects in the center for epidemiologic studies depression (CES-D) scale: personal digital assistant vs. paper and pencil administration , 2007, Quality of Life Research.
[13] Amy P Abernethy,et al. Commentary: encouraging clinicians to incorporate longitudinal patient-reported symptoms in routine clinical practice. , 2011, Journal of oncology practice.
[14] A. Garratt,et al. Patient experiences with information in a hospital setting: Associations with coping and self-rated health in chronic illness , 2006, Quality of Life Research.
[15] Galina Velikova,et al. Measuring quality of life in routine oncology practice improves communication and patient well-being: a randomized controlled trial. , 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[16] Sydney M. Dy,et al. Asking the right questions: investigating needs assessments and health-related quality-of-life questionnaires for use in oncology clinical practice , 2007, Supportive Care in Cancer.
[17] A Simon Pickard,et al. Proxy Evaluation of Health-Related Quality of Life: A Conceptual Framework for Understanding Multiple Proxy Perspectives , 2005, Medical care.
[18] G. Guyatt,et al. The impact of measuring patient-reported outcomes in clinical practice: a systematic review of the literature , 2008, Quality of Life Research.
[19] X. Badia,et al. Effect of Mode of Administration on I–PSS Scores in a Large BPH Patient Population , 2001, European Urology.
[20] M. Kochen,et al. A systematic review: how to choose appropriate health-related quality of life (HRQOL) measures in routine general practice? , 2005, Journal of Zhejiang University. Science. B.
[21] J. Vonk,et al. Day-to-day measurement of patient-reported outcomes in exacerbations of chronic obstructive pulmonary disease , 2013, International journal of chronic obstructive pulmonary disease.
[22] Ron D. Hays,et al. Don’t middle your MIDs: regression to the mean shrinks estimates of minimally important differences , 2014, Quality of Life Research.
[23] Ron D Hays,et al. Evaluating the Statistical Significance of Health-Related Quality-Of-Life Change in Individual Patients , 2005, Evaluation & the health professions.
[24] Gillian King,et al. The Internet is valid and reliable for child-report: an example using the Activities Scale for Kids (ASK) and the Pediatric Quality of Life Inventory (PedsQL). , 2009, Journal of clinical epidemiology.
[25] Frank J. Snoek,et al. Monitoring and Discussing Health-Related Quality of Life in Adolescents With Type 1 Diabetes Improve Psychosocial Well-Being , 2008, Diabetes Care.
[26] Kathryn M McPherson,et al. Assessment of quality of life and participation within an outpatient rehabilitation setting , 2009, Disability and rehabilitation.
[27] Victor M Montori,et al. Harmonizing and consolidating the measurement of patient-reported information at health care institutions: a position statement of the Mayo Clinic , 2014, Patient related outcome measures.
[28] D. Osoba,et al. Translating the science of patient-reported outcomes assessment into clinical practice. , 2007, Journal of the National Cancer Institute. Monographs.
[29] John Dowling,et al. Interview vs. paper-and-pencil administration of the McGill pain questionnaire , 1981, PAIN.
[30] D Feldman-Stewart,et al. Communicating quality of life information to cancer patients: a study of six presentation formats. , 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[31] Lotte Haverman,et al. Effectiveness of a Web-Based Application to Monitor Health-Related Quality of Life , 2013, Pediatrics.
[32] Lotte Haverman,et al. Development and implementation of a patient reported outcome intervention (QLIC-ON PROfile) in clinical paediatric oncology practice. , 2010, Patient education and counseling.
[33] Gordon H Guyatt,et al. Exploration of the value of health-related quality-of-life information from clinical research and into clinical practice. , 2007, Mayo Clinic proceedings.
[34] N. Aaronson,et al. Effects of mode of administration (MOA) on the measurement properties of the EORTC QLQ-C30: a randomized study , 2010, Health and quality of life outcomes.
[35] Milo A Puhan,et al. Interviewer versus self-administered health-related quality of life questionnaires - Does it matter? , 2011, Health and quality of life outcomes.
[36] Yang Liu,et al. PROMIS® Parent Proxy Report Scales: an item response theory analysis of the parent proxy report item banks , 2012, Quality of Life Research.
[37] R. Gershon,et al. The future of outcomes measurement: item banking, tailored short-forms, and computerized adaptive assessment , 2007, Quality of Life Research.
[38] H. Duivenvoorden,et al. Effectiveness of health-related quality-of-life measurement in clinical practice: a prospective, randomized controlled trial in patients with chronic liver disease and their physicians , 2008, Quality of Life Research.
[39] P. Fayers,et al. Evaluating the effectiveness of using PROs in clinical practice: a role for cluster-randomised trials , 2008, Quality of Life Research.
[40] Richard Norman,et al. Does mode of administration matter? Comparison of online and face-to-face administration of a time trade-off task , 2010, Quality of Life Research.
[41] Anthony L Back,et al. Electronic self-report assessment for cancer and self-care support: results of a multicenter randomized trial. , 2014, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[42] M. Donaldson,et al. Taking PROs and patient-centered care seriously: incremental and disruptive ideas for incorporating PROs in oncology practice , 2008, Quality of Life Research.
[43] Lotte Haverman,et al. Monitoring health-related quality of life in paediatric practice: development of an innovative web-based application , 2011, BMC pediatrics.
[44] I J Higginson,et al. Using quality of life measures in the clinical setting , 2001, BMJ : British Medical Journal.
[45] Otto B. Walter,et al. Development and evaluation of a computer adaptive test for ‘Anxiety’ (Anxiety-CAT) , 2007, Quality of Life Research.
[46] Jonathan Sussman,et al. Multidisciplinary health care professionals' perceptions of the use and utility of a symptom assessment system for oncology patients. , 2011, Journal of oncology practice.
[47] C. Dowrick,et al. Does testing for depression influence diagnosis or management by general practitioners? , 1995, Family practice.
[48] J H Wasson,et al. A randomized trial of the use of patient self-assessment data to improve community practices. , 1999, Effective clinical practice : ECP.
[49] P. Ubel,et al. Reducing the Influence of Anecdotal Reasoning on People’s Health Care Decisions: Is a Picture Worth a Thousand Statistics? , 2005, Medical decision making : an international journal of the Society for Medical Decision Making.
[50] L. Kalra,et al. Who should measure quality of life? , 2001, BMJ : British Medical Journal.
[51] Matthias Rose,et al. Logistics of collecting patient-reported outcomes (PROs) in clinical practice: an overview and practical examples , 2009, Quality of Life Research.
[52] Hua Zheng,et al. Integrating Patient-reported Outcomes Into Orthopaedic Clinical Practice: Proof of Concept From FORCE-TJR , 2013, Clinical orthopaedics and related research.
[53] A. Bezjak,et al. Cancer patients' preferences for communicating clinical trial quality of life information: A qualitative study , 2003, Quality of Life Research.
[54] N. Aaronson,et al. Use of health‐related quality‐of‐life assessments in daily clinical oncology nursing practice , 2008, Cancer.
[55] Michael Friedman,et al. Developing brief scales for use in clinical practice: the reliability and validity of single-item self-report measures of depression symptom severity, psychosocial impairment due to depression, and quality of life. , 2006, The Journal of clinical psychiatry.
[56] Kathleen N. Lohr,et al. Using patient-reported outcomes in clinical practice: challenges and opportunities , 2009, Quality of Life Research.
[57] Albert W Wu,et al. When using patient-reported outcomes in clinical practice, the measure matters: a randomized controlled trial. , 2014, Journal of oncology practice.
[58] Victor M Montori,et al. Perspective: The Role of Numeracy in Health Care , 2008, Journal of health communication.
[59] F Davidoff,et al. Toward stronger evidence on quality improvement. Draft publication guidelines: the beginning of a consensus project , 2005, Quality and Safety in Health Care.
[60] Sherry Holcomb,et al. Validation of the EQ-5D quality of life instrument in patients after myocardial infarction , 2005, Quality of Life Research.
[61] Qiuling Shi,et al. Automated symptom alerts reduce postoperative symptom severity after cancer surgery: a randomized controlled clinical trial. , 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[62] A Donner,et al. Statistical considerations in the design and analysis of community intervention trials. , 1996, Journal of clinical epidemiology.
[63] C. McHorney,et al. Health status assessment methods for adults: past accomplishments and future challenges. , 1999, Annual review of public health.
[64] References , 1971 .
[65] Sheilah Hogg-Johnson,et al. Minimal change is sensitive, less specific to recovery: a diagnostic testing approach to interpretability. , 2011, Journal of clinical epidemiology.
[66] N. Aaronson,et al. Health-related quality-of-life assessments and patient-physician communication: a randomized controlled trial. , 2002, JAMA.
[67] M. Stek,et al. The American Urological Association symptom index: does mode of administration affect its psychometric properties? , 1995, The Journal of urology.
[68] Amy P Abernethy,et al. Supporting clinical practice decisions with real-time patient-reported outcomes. , 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[69] Simon Gilbody,et al. Should we screen for depression? , 2006, BMJ : British Medical Journal.
[70] David Feeny,et al. Assessing the use of health-related quality of life measures in the routine clinical care of lung-transplant patients , 2010, Quality of Life Research.
[71] Lisa M. Schwartz,et al. The Role of Numeracy in Understanding the Benefit of Screening Mammography , 1997, Annals of Internal Medicine.
[72] R. Sheldon,et al. Statistical issues encountered in the comparison of health-related quality of life in diseased patients to published general population norms: problems and solutions. , 1999, Journal of clinical epidemiology.
[73] Christopher J. McCarthy,et al. Paper-and-Pencil Or Online? , 2002, Assessment.
[74] J. Ankri,et al. Agreement between patients' and proxies' reports of quality of lifein Alzheimer's disease , 2004, Quality of Life Research.
[75] B. Parasuraman,et al. Electronic Versus Paper Questionnaires: A Further Comparison in Persons with Asthma , 2003, The Journal of asthma : official journal of the Association for the Care of Asthma.
[76] M. Donaldson,et al. Using patient-reported outcomes in clinical oncology practice: benefits, challenges and next steps , 2006, Expert review of pharmacoeconomics & outcomes research.
[77] Albert W Wu,et al. What can I do? Recommendations for responding to issues identified by patient-reported outcomes assessments used in clinical practice. , 2012, The journal of supportive oncology.
[78] D. Campbell,et al. EXPERIMENTAL AND QUASI-EXPERIMENT Al DESIGNS FOR RESEARCH , 2012 .
[79] R. Hays,et al. Prospects and challenges in using patient-reported outcomes in clinical practice , 2008, Quality of Life Research.
[80] F. Davidoff,et al. What is “quality improvement” and how can it transform healthcare? , 2007, Quality and Safety in Health Care.
[81] L W Chambers,et al. Sensitivity to Change and the Effect of Mode of Administration on Health Status Measurement , 1987, Medical care.
[82] David Feeny,et al. Effects of mode and order of administration on generic health-related quality of life scores. , 2009, Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research.
[83] Lea Maes,et al. Comparison of a computer-administered and paper-and-pencil-administered questionnaire on health and lifestyle behaviors. , 2006, The Journal of adolescent health : official publication of the Society for Adolescent Medicine.
[84] M. Donaldson,et al. Use of Patient‐Reported Outcomes in Clinical Oncology Practice: A Nonvisit Approach to Patient Care Based on the IOM Report , 2007, The Journal of ambulatory care management.
[85] H A Guess,et al. Does the mode of questionnaire administration affect the reporting of urinary symptoms? , 1995, Urology.
[86] Nicholas J. Talley,et al. Patient reported outcomes in gastroesophageal reflux disease: An overview of available measures , 2005, Quality of Life Research.
[87] Aziz Sheikh,et al. Concordance between supervised and postal administration of the Mini Asthma Quality of Life Questionnaire (MiniAQLQ) and Asthma Control Questionnaire (ACQ) was very high. , 2005, Journal of clinical epidemiology.
[88] Bernhard Holzner,et al. Do neurooncological patients and their significant others agree on quality of life ratings? , 2009, Health and quality of life outcomes.
[89] Matthias Rose,et al. Method of administration of PROMIS scales did not significantly impact score level, reliability, or validity. , 2014, Journal of clinical epidemiology.
[90] Julian Thumboo,et al. Quality of life scores differed according to mode of administration in a review of three major oncology questionnaires. , 2006, Journal of clinical epidemiology.
[91] W. Kapoor,et al. Patient Difficulty Using Tablet Computers to Screen in Primary Care , 2008, Journal of General Internal Medicine.
[92] L. Delbeke. Quasi-experimentation - design and analysis issues for field settings - cook,td, campbell,dt , 1980 .
[93] Ethan Basch,et al. Electronic patient‐reported outcome systems in oncology clinical practice , 2012, CA: a cancer journal for clinicians.
[94] R Lilford,et al. Effects of redesigned community postnatal care on womens' health 4 months after birth: a cluster randomised controlled trial , 2002, The Lancet.
[95] Gary Donaldson,et al. Patient-reported outcomes and the mandate of measurement , 2008, Quality of Life Research.
[96] C. Shaw,et al. Mode of data elicitation, acquisition and response to surveys: a systematic review. , 2012, Health technology assessment.
[97] A Smith,et al. Feasibility and compliance of automated measurement of quality of life in oncology practice. , 2003, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[98] David M. Murray,et al. Design and Analysis of Group- Randomized Trials , 1998 .
[99] E H Wagner,et al. Chronic disease management: what will it take to improve care for chronic illness? , 1998, Effective clinical practice : ECP.
[100] Rachel Hess,et al. A Randomized Controlled Pilot Trial of the Functional Assessment Screening Tablet to Engage Patients at the Point of Care , 2014, Journal of General Internal Medicine.
[101] Janel Hanmer,et al. Mode of Administration Is Important in US National Estimates of Health-Related Quality of Life , 2007, Medical care.
[102] Joseph C Cappelleri,et al. Applying quality-of-life data formally and systematically into clinical practice. , 2007, Mayo Clinic proceedings.
[103] A Simon Pickard,et al. Proxy Assessment of Health-Related Quality of Life in African American and White Respondents With Prostate Cancer: Perspective Matters , 2009, Medical care.
[104] Vilai Kuptniratsaikul,et al. Anxiety and depressive symptoms after stroke in 9 rehabilitation centers. , 2008, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.
[105] Joanne Greenhalgh,et al. Tacit and encoded knowledge in the use of standardised outcome measures in multidisciplinary team decision making: a case study of in-patient neurorehabilitation. , 2008, Social science & medicine.
[106] Bryant T Karras,et al. Enhancing patient-provider communication with the electronic self-report assessment for cancer: a randomized trial. , 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[107] Yvonne Birks,et al. Pitfalls in the interpretation of standardised quality of life instruments for individual patients? A qualitative study in colorectal cancer , 2013, Quality of Life Research.
[108] G R Baker,et al. Strengthening the contribution of quality improvement research to evidence based health care , 2006, Quality and Safety in Health Care.
[109] A. Wu,et al. The effect of mode of administration on Medical Outcomes Study health ratings and EuroQol scores in AIDS , 2004, Quality of Life Research.
[110] Albert W Wu,et al. The Use of Patient-reported Outcomes (PRO) Within Comparative Effectiveness Research: Implications for Clinical Practice and Health Care Policy , 2012, Medical care.
[111] Eugene C Nelson,et al. Good Measurement for Good Improvement Work , 2004, Quality management in health care.
[112] Jeffrey W. Jutai,et al. Psychosocial Impact of Assistive Devices Scale , 2016 .
[113] H. Putter,et al. Effectiveness of the introduction of an International Classification of Functioning, Disability and Health-based rehabilitation tool in multidisciplinary team care in patients with rheumatoid arthritis. , 2007, Arthritis and rheumatism.
[114] Allan Donner,et al. Design and Analysis of Cluster Randomization Trials in Health Research , 2001 .
[115] R L Street,et al. Using Health Status Surveys in Medical Consultations , 1994, Medical care.
[116] K Magruder-Habib,et al. Improving Physicians' Recognition and Treatment of Depression in General Medical Care: Results From a Randomized Clinical Trial , 1990, Medical care.
[117] Lars Hansson,et al. Structured patient–clinician communication and 1-year outcome in community mental healthcare , 2007, British Journal of Psychiatry.
[118] N K Aaronson,et al. Quality of life assessment in daily clinical oncology practice: a feasibility study. , 1998, European journal of cancer.
[119] Joann G. Elmore,et al. Open Notes: Doctors and Patients Signing On , 2010, Annals of Internal Medicine.
[120] J. Foley,et al. Redefining functionality and treatment efficacy in multiple sclerosis , 2009, Neurology.
[121] L. von Essen,et al. Measuring health-related quality of life in adolescents and young adults: Swedish normative data for the SF-36 and the HADS, and the influence of age, gender, and method of administration , 2006, Health and quality of life outcomes.
[122] S. Acaster,et al. Methods for interpreting change over time in patient-reported outcome measures , 2013, Quality of Life Research.
[123] G. Kemmler,et al. A new approach to combining clinical relevance and statistical significance for evaluation of quality of life changes in the individual patient. , 2010, Journal of clinical epidemiology.
[124] John H Wasson,et al. A Controlled Trial of Methods for Managing Pain in Primary Care Patients With or Without Co-Occurring Psychosocial Problems , 2006, The Annals of Family Medicine.
[125] P S Kurtin,et al. Monitoring dialysis patients' health status. , 1994, American journal of kidney diseases : the official journal of the National Kidney Foundation.
[126] David Cella,et al. A Randomized Study of Electronic Diary versus Paper and Pencil Collection of Patient-Reported Outcomes in Patients with Non-Small Cell Lung Cancer , 2008, The patient.
[127] V. Duyan,et al. Effects of sociodemographic characteristics, illness process, and social support on the levels of perceived quality of life in veterans. , 2006, Military medicine.
[128] Albert W. Wu,et al. Advances in the Use of Patient Reported Outcome Measures in , 2013 .
[129] Sandra E. Black,et al. Utility-based Quality of Life Measures in Alzheimer’s Disease , 2006, Quality of Life Research.
[130] Chih-Hung Chang,et al. Patient-reported outcomes measurement and management with innovative methodologies and technologies , 2007, Quality of Life Research.
[131] Robyn Attewell,et al. A comparison of an electronic version of the SF-36 General Health Questionnaire to the standard paper version , 2002, Quality of Life Research.
[132] Sydney M. Dy,et al. Needs assessments can identify scores on HRQOL questionnaires that represent problems for patients: an illustration with the Supportive Care Needs Survey and the QLQ-C30 , 2010, Quality of Life Research.
[133] Donald Berwick,et al. Developing and Testing Changes in Delivery of Care , 1998, Annals of Internal Medicine.
[134] Laurence H. Baker,et al. Clinical Trials: Design, Conduct, and Analysis , 1987 .
[135] P. Sandercock,et al. Framework for design and evaluation of complex interventions to improve health , 2000, BMJ : British Medical Journal.
[136] Roxanne Jensen,et al. PatientViewpoint: a website for patient-reported outcomes assessment , 2009, Quality of Life Research.
[137] Jeanne M. Landgraf,et al. Feasibility, reliability, and validity of adolescent health status measurement by the Child Health Questionnaire Child Form (CHQ-CF): internet administration compared with the standard paper version , 2007, Quality of Life Research.
[138] P. Ewell. No Significant Difference , 1999 .
[139] R. Fitzpatrick,et al. Impact of patient-reported outcome measures on routine practice: a structured review. , 2006, Journal of evaluation in clinical practice.
[140] ZOE HILDON,et al. Impact of format and content of visual display of data on comprehension, choice and preference: a systematic review. , 2012, International journal for quality in health care : journal of the International Society for Quality in Health Care.
[141] Hiroko Yamashita,et al. Using the EORTC-QLQ-C30 in clinical practice for patient management: identifying scores requiring a clinician’s attention , 2013, Quality of Life Research.
[142] J. Fortenberry,et al. Comparability of a computer-assisted versus written method for collecting health behavior information from adolescent patients. , 1999, The Journal of adolescent health : official publication of the Society for Adolescent Medicine.
[143] Reyis Kurt,et al. Computer-assisted assessment of depression and function in older primary care patients , 2004, Comput. Methods Programs Biomed..
[144] K. Meadows,et al. The effectiveness of the use of patient-based measures of health in routine practice in improving the process and outcomes of patient care: a literature review. , 1999, Journal of evaluation in clinical practice.
[145] Ramesh Farzanfar,et al. Automated monitoring of symptoms during ambulatory chemotherapy and oncology providers’ use of the information: a randomized controlled clinical trial , 2014, Supportive Care in Cancer.
[146] C. Moinpour,et al. Development, feasibility and compliance of a web-based system for very frequent QOL and symptom home self-assessment after hematopoietic stem cell transplantation , 2005, Quality of Life Research.
[147] G J Martin,et al. Impact of screening for mental health concerns on health service utilization and functional status in primary care patients. , 1996, Archives of internal medicine.
[148] Ron D Hays,et al. Equivalence of mail and telephone responses to the CAHPS Hospital Survey. , 2005, Health services research.
[149] M. Eaton,et al. Surrogate decision making for genetic testing for Alzheimer disease. , 1999, Genetic testing.
[150] David Cella,et al. Recommendations on evidence needed to support measurement equivalence between electronic and paper-based patient-reported outcome (PRO) measures: ISPOR ePRO Good Research Practices Task Force report. , 2009, Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research.
[151] Michael Seid,et al. Reliability, Validity, and Responsiveness of the Pediatric Quality of Life Inventory™ (PedsQL™) Generic Core Scales and Asthma Symptoms Scale in Vulnerable Children With Asthma , 2010, The Journal of asthma : official journal of the Association for the Care of Asthma.
[152] Ingrid Mühlhauser,et al. What constitutes evidence-based patient information? Overview of discussed criteria. , 2010, Patient education and counseling.
[153] J Alonso,et al. Provision of feedback on perceived health status to health care professionals: a systematic review of its impact. , 2000, Medical care.
[154] W. Gaissmaier,et al. Numbers can be worth a thousand pictures: individual differences in understanding graphical and numerical representations of health-related information. , 2012, Health psychology : official journal of the Division of Health Psychology, American Psychological Association.
[155] Sebastian Muller,et al. Statistical Design For Research , 2016 .
[156] G P Samsa,et al. Are health-related quality-of-life measures affected by the mode of administration? , 1996, Journal of clinical epidemiology.
[157] Hadi Kharrazi,et al. Measure once, cut twice d adding patient-reported outcome measures to the electronic health record for comparative effectiveness research , 2013 .
[158] J. Verhoef,et al. The impact of introducing an ICF-based rehabilitation tool on staff satisfaction with multidisciplinary team care in rheumatology: an exploratory study , 2008, Clinical rehabilitation.
[159] J. M. McCoy,et al. Improving patient quality of life with feedback to physicians about functional status , 1995, Journal of General Internal Medicine.
[160] Joanne Greenhalgh,et al. The use of patient reported outcome measures in routine clinical practice: lack of impact or lack of theory? , 2005, Social science & medicine.