The Patient-Reported Outcomes Measurement Information System (PROMIS): progress of an NIH Roadmap cooperative group during its first two years
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Cardiovascular disease self-care interventionsRoutine provision of information on patient-reported outcome measures to healthcare providers and patients in clinical practiceReview of patient-reported outcome measures in chronic hepatitis CPatient reported outcomes in rheumatoid arthritis clinical trialsFurthering the reliable and valid measurement of mental health screening, diagnoses, treatment and outcomes through health information technologyPatient-reported outcomes in routine cancer clinical practice: a scoping review of use, impact on health outcomes, and implementation factorsCapturing and Incorporating Patient-Reported Outcomes into Clinical Trials: Practical Considerations for CliniciansAssessment of chronic postsurgical pain after knee replacement: a systematic reviewApproaches for estimating minimal clinically important differences in systemic lupus erythematosusIntegrating Patient-Reported Outcomes into Spine Surgical Care through Visual Dashboards: Lessons Learned from Human-Centered DesignSharing behavioral data through a grid infrastructure using data standardsValidation of PROMIS ® Physical Function computerized adaptive tests for orthopaedic foot and ankle outcome research.Communicating advanced cancer patients' symptoms via the Internet: a pooled analysis of two randomized trials examining caregiver preparedness, physical burden, and negative mood.Gaps in Aging Research as it Applies to Rheumatologic Clinical Care.Hypertension with unsatisfactory sleep health (HUSH): study protocol for a randomized controlled trial.The e-MSWS-12: improving the multiple sclerosis walking scale using item response theory.Longitudinal patterns of cancer patient reported outcomes in end of life care predict survivalClinical Implications of a Dimensional Approach: The Normal:Abnormal Spectrum of Early Irritability.Introduction: cognitive dysfunction in multiple sclerosisPutting theory to the test: modeling a multidimensional, developmentally-based approach to preschool disruptive behaviorComputerized adaptive testing for follow-up after discharge from inpatient rehabilitation: II. Participation outcomes.Developing the communicative participation item bank: Rasch analysis results from a spasmodic dysphonia sample.Measuring organizational and individual factors thought to influence the success of quality improvement in primary care: a systematic review of instruments.Qualitative analysis of patients' feedback from a PROMs survey of cancer patients in England.Developing core outcomes sets: methods for identifying and including patient-reported outcomes (PROs).Procurement of shared data instruments for Research Electronic Data Capture (REDCap).Cross cultural adaptation and validation of a Spanish version of the Lower Limb Functional IndexMeasuring health-related quality of life in chronic obstructive pulmonary disease: properties of the EQ-5D-5L and PROMIS-43 short formInstruments to assess patient satisfaction after teleconsultation and triage: a systematic review.Subjective well-being measures for children were developed within the PROMIS project: presentation of first results.Qualitative Evaluation of Pediatric Pain Behavior, Quality, and Intensity Item Candidates and the PROMIS Pain Domain Framework in Children With Chronic Pain.Contributions of physical function and satisfaction with social roles to emotional distress in chronic pain: a Collaborative Health Outcomes Information Registry (CHOIR) studyPROMIS measures of pain, fatigue, negative affect, physical function, and social function demonstrated clinical validity across a range of chronic conditions.Recommendations for a first Core Outcome Measurement set for complex regional PAin syndrome Clinical sTudies (COMPACT).Making the Oxford Hip and Knee Scores meaningful at the patient level through normative scoring and registry data.Mortality Risk Prediction: Can Comorbidity Indices Be Improved With Psychosocial Data?Parental Assessment of Status of Congenital Upper Limb Differences: Analysis of the Pediatric Outcomes Data Collection InstrumentDevelopment of a validated patient-reported symptom metric for pediatric eosinophilic esophagitis: qualitative methods.Generalizing Treatment Effect Estimates From Sample to Population: A Case Study in the Difficulties of Finding Sufficient Data.Integrating Patient-Generated Health Data Into Clinical Care Settings or Clinical Decision-Making: Lessons Learned From Project HealthDesign
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P2860
The Patient-Reported Outcomes Measurement Information System (PROMIS): progress of an NIH Roadmap cooperative group during its first two years
description
2007 nî lūn-bûn
@nan
2007 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
The Patient-Reported Outcomes ...... oup during its first two years
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The Patient-Reported Outcomes ...... oup during its first two years
@en
The Patient-Reported Outcomes ...... oup during its first two years
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label
The Patient-Reported Outcomes ...... oup during its first two years
@ast
The Patient-Reported Outcomes ...... oup during its first two years
@en
The Patient-Reported Outcomes ...... oup during its first two years
@nl
prefLabel
The Patient-Reported Outcomes ...... oup during its first two years
@ast
The Patient-Reported Outcomes ...... oup during its first two years
@en
The Patient-Reported Outcomes ...... oup during its first two years
@nl
P2093
P2860
P3181
P1433
P1476
The Patient-Reported Outcomes ...... oup during its first two years
@en
P2093
Bonnie Bruce
Bryce Reeve
Deborah Ader
James F Fries
Karon Cook
Mattias Rose
Nan Rothrock
Richard Gershon
Susan Yount
P2860
P304
P3181
P356
10.1097/01.MLR.0000258615.42478.55
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P433
P50
P577
2007-05-01T00:00:00Z