The Patient-Reported Outcomes Measurement Information System (PROMIS): progress of an NIH Roadmap cooperative group during its first two years - Test2 - elhamkhani - TriplyDB

The Patient-Reported Outcomes Measurement Information System (PROMIS): progress of an NIH Roadmap cooperative group during its first two years

The Patient-Reported Outcomes Measurement Information System (PROMIS): progress of an NIH Roadmap cooperative group during its first two years

http://www.wikidata.org/entity/Q24634716

about

Cardiovascular disease self-care interventions Routine provision of information on patient-reported outcome measures to healthcare providers and patients in clinical practice Review of patient-reported outcome measures in chronic hepatitis C Patient reported outcomes in rheumatoid arthritis clinical trials Furthering the reliable and valid measurement of mental health screening, diagnoses, treatment and outcomes through health information technology Patient-reported outcomes in routine cancer clinical practice: a scoping review of use, impact on health outcomes, and implementation factors Capturing and Incorporating Patient-Reported Outcomes into Clinical Trials: Practical Considerations for Clinicians Assessment of chronic postsurgical pain after knee replacement: a systematic review Approaches for estimating minimal clinically important differences in systemic lupus erythematosus Integrating Patient-Reported Outcomes into Spine Surgical Care through Visual Dashboards: Lessons Learned from Human-Centered Design Sharing behavioral data through a grid infrastructure using data standards Validation 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 survival Clinical Implications of a Dimensional Approach: The Normal:Abnormal Spectrum of Early Irritability.Introduction: cognitive dysfunction in multiple sclerosis Putting theory to the test: modeling a multidimensional, developmentally-based approach to preschool disruptive behavior Computerized 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 Index Measuring health-related quality of life in chronic obstructive pulmonary disease: properties of the EQ-5D-5L and PROMIS-43 short form Instruments 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) study PROMIS 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 Instrument Development 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

P2860

Q23923299-4D89AFC4-5AF5-4F3A-B8B2-3810DD859206 Q24186707-B095DEED-29A4-435A-851F-7732B759F984 Q26828825-4F59782B-9DD6-411A-8536-14A60F8C7CEC Q26852960-B1D55CEF-41AB-4481-991B-598C60135AAA Q26864764-3803F405-10DA-485C-A43A-98716A25AC12 Q27004014-0E82C498-FC8C-472F-88FF-B1266D28E2AE Q27007773-004D3BDF-D3E3-4FB1-AC22-D5DCAAA562D2 Q27008476-D9D6594E-DB67-4F84-8D27-030F223EBF2F Q27021623-69FE1E66-4145-4B55-96C5-E07D2A329EA5 Q28647471-AE1D1476-2EE4-4C0E-84DD-49B30359AA00 Q28656438-0F51C10E-C141-426E-BC16-FF011C8B9169 Q28675887-FBFBCF39-108F-4284-98BF-8A778BBF44EC Q30224051-98F0BEAE-B72B-4FEB-94C6-785A7B82C570 Q30240678-C78EB6FA-665A-4328-BD76-4F35A744431A Q30252196-C56D5B02-441C-484B-8B73-D28E918B7EA0 Q30276511-DAD3514E-AF19-4643-AD99-5DBE080909CD Q30278080-253C1E3C-A780-41A1-ADAC-84225D9D6A33 Q30357348-647CBF77-1339-4F6D-A60D-057E3F9BB417 Q30415225-1088303A-C428-4F27-AC0E-A80ECC9D7646 Q30418895-D6359DFF-808E-4788-86CC-D5A0473AF93A Q30439889-CB00436F-12CA-45AC-A5A2-0B0621DFA245 Q30475861-2108DB23-3A29-4A53-B32F-2B2A3418B482 Q30535829-17AC7A0A-1AC2-4548-878E-5C4F66C5F511 Q30539378-2A226C12-B22A-465F-8F5C-D1419269AF0F Q30571178-5D8BCE7B-4910-4B0D-854A-CDAC6DC0C26E Q30577350-B34D5F52-9B95-4E76-A51C-5DE67F5642CD Q30579250-FD85FDBC-624F-4139-AE57-1C9F913FC4F5 Q30581735-4EBC4809-8BB5-4FFE-A6C7-E74B358F4E56 Q30582266-F82C6039-6469-4876-9540-ED7B779A772D Q30585780-C883CB87-EFC2-470A-B93E-096C839E84F5 Q30684690-87619283-5F72-4A55-8D48-26AAC17D7932 Q30782152-A5B48AEA-A92C-4AB6-9025-D8F85006B3F4 Q30830391-F1F94332-E230-4FE6-828B-799C5C55303C Q30852024-D51D2BB1-0158-4072-8151-88A0A6E44BD2 Q30989982-DCFFE770-3B1B-493C-89A8-81F29DDD39E3 Q30999448-C61D6F4F-F5A5-4970-B949-8887077E07C2 Q31038273-3E019E6C-9554-4F13-B7A1-F4C9F13B4897 Q31041358-7FC6A7B2-2C05-474B-B9FE-F0D98C0EC441 Q31119659-801CC71C-026D-4345-BFE1-012EDE0517D0 Q31137776-EFB5F8F1-FAB0-44AA-B6E7-4AE0435FD49E

P2860

The Patient-Reported Outcomes Measurement Information System (PROMIS): progress of an NIH Roadmap cooperative group during its first two years

http://www.wikidata.org/entity/Q24634716

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

@ast

The Patient-Reported Outcomes ...... oup during its first two years

@en

The Patient-Reported Outcomes ...... oup during its first two years

@nl

type

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

P1433

Q24634716-7F2521A9-6D3D-43AA-B6B1-760BB0CC60B5

P1476

Q24634716-86BF0762-550B-44F3-8E7A-7F536460830D

P2093

Q24634716-04895B83-774F-4B13-947D-131784262E29

Q24634716-06ACF378-A701-4A69-B19F-1A7E98A5491E

Q24634716-0797C219-87D3-41ED-BC2B-E512F91FE79D

Q24634716-17C2F813-EC45-4D21-8BC9-481F935F188E

Q24634716-37C11771-06D5-45DA-99E5-BFF168C9A4AF

Q24634716-71B96C81-393E-40AA-B26E-432ACE99DC50

Q24634716-83C77BBA-4371-44CE-85EE-2A3ECBDD0EA0

Q24634716-A4500756-F5D0-4D3D-BD5E-4B2021A9356E

Q24634716-C6639DF3-2CFE-4522-AEF9-CD830F73DA2F

P2860

Q24634716-197A4961-3DB1-405E-A72E-CA883BCF08C6

Q24634716-25050D01-3C6C-4356-AA26-C4F40D6556F8

Q24634716-2932C70E-390A-4AE6-BD9B-DEE177E11205

Q24634716-40011AA6-B2DB-4C20-A848-FA4881537DFD

Q24634716-40363F16-1E98-4CC0-80A0-9750493AE1C7

Q24634716-4870DF2C-D761-44FD-B691-C52763F385AC

Q24634716-76E9D0D4-60B3-4ECE-86D7-D47F925DD5F4

Q24634716-8852FF82-A491-4E60-89A3-2916678954AD

Q24634716-8F1085A3-91CC-4BF1-9DDE-7D5F3747F90B

Q24634716-C070F29C-AA4C-4F9D-92F2-D7734858D274

P304

Q24634716-1A0E7180-BAE2-41D7-AD54-3702C83E8A75

P31

Q24634716-8A513856-856D-4822-B908-2EE74480410E

P3181

Q24634716-763C93DC-65B2-48F0-8DCF-0C106AC65EC2

P356

Q24634716-AA5679E5-C8FD-4C80-8AAA-7A5AFC73A4DE

P407

Q24634716-569EC8AE-E819-4F78-872B-F87E8CE94731

P433

Q24634716-1065AC71-D58F-441F-9E35-34D30C7D08CE

P478

Q24634716-3401FCA6-0C4E-46C9-A165-F6DE758CC841

P50

Q24634716-FD6CDAB2-C0CC-4746-91CA-C320C5181FC3

P577

Q24634716-7E939643-42FF-45CC-AA3C-58EADEA5F0CB

P698

Q24634716-6193D08D-5256-4534-9387-06697EB91839

P921

Q24634716-7C7B5973-7E0A-4B8F-8C3E-C87126FCCD43

P932

Q24634716-3F5E3B60-E6D0-4EBC-A63F-FA7137B155FB

P3181

P356

01.MLR.0000258615.42478.55

P1433

P1476

The Patient-Reported Outcomes ...... oup during its first two years

@en

P2093

Bonnie Bruce

http://www.w3.org/2001/XMLSchema#string

Bryce Reeve

http://www.w3.org/2001/XMLSchema#string

Deborah Ader

http://www.w3.org/2001/XMLSchema#string

James F Fries

http://www.w3.org/2001/XMLSchema#string

Karon Cook

http://www.w3.org/2001/XMLSchema#string

Mattias Rose

http://www.w3.org/2001/XMLSchema#string

Nan Rothrock

http://www.w3.org/2001/XMLSchema#string

Richard Gershon

http://www.w3.org/2001/XMLSchema#string

Susan Yount

http://www.w3.org/2001/XMLSchema#string

P2860

Item banking to improve, shorten and computerize self-reported fatigue: an illustration of steps to create a core item bank from the FACIT-Fatigue Scale.

An item response theory-based pain item bank can enhance measurement precision.

Evaluation of item candidates: the PROMIS qualitative item review.

Considerations for developing interfaces for collecting patient-reported outcomes that allow the inclusion of individuals with disabilities

Item response theory and health outcomes measurement in the 21st century.

Psychometric evaluation and calibration of health-related quality of life item banks: plans for the Patient-Reported Outcomes Measurement Information System (PROMIS).

Methods of assessing prevalent cardiovascular disease in the Cardiovascular Health Study.

Item response theory analyses of physical functioning items in the medical outcomes study.

The promise of PROMIS: using item response theory to improve assessment of patient-reported outcomes.

Calibration of an item pool for assessing the burden of headaches: an application of item response theory to the headache impact test (HIT).

P304

S3-S11

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P3181

652998

http://www.w3.org/2001/XMLSchema#string

P356

10.1097/01.MLR.0000258615.42478.55

http://www.w3.org/2001/XMLSchema#string

P407

P433

5 Suppl 1

http://www.w3.org/2001/XMLSchema#string

P478

45

http://www.w3.org/2001/XMLSchema#string

P50

P577

2007-05-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

17443116

http://www.w3.org/2001/XMLSchema#string

P921

P932

2829758

http://www.w3.org/2001/XMLSchema#string