Roxanne E Jensen
Dados Biográficos
| ID | 5542435 |
|---|---|
| NOME | Roxanne E Jensen |
| PRENOMES | Roxanne E |
| SOBRENOME | Jensen |
| ASSINATURA | JENSEN R E |
| AFILIAÇÕES | Georgetown University |
| ORCID | 0000-0002-4632-1091 |
| VERIFICADO | Sim |
| TOTAL DE OBRAS | 12 |
| TOTAL DE CITAÇÕES | 0 |
| TOTAL COMO AUTOR | 12 |
| TOTAL COMO EDITOR | 0 |
| PRIMEIRO ANO DE PUBLICAÇÃO | 2007 |
| ANO MAIS RECENTE DE PUBLICAÇÃO | 2024 |
| ÍNDICE H | 0 |
Salivary, lacrimal and nasal (Salans) measure to assess side effects following radioactive iodine treatment
Examination of individual and multiple comorbid conditions and health-related quality of life in older cancer survivors
Applying PRO Reference Values to Communicate Clinically Relevant Information at the Point-of-care
INTRODUCTION: The inclusion of reference values for common patient-reported outcomes (PROs) measures in clinical care settings provides a clinically relevant context for an individual patient's PRO scores. PRO reference values are currently not reported in clinical care settings. This is a missed opportunity, as clinicians are familiar with the presence and interpretation of reference values, commonly provided alongside laboratory test results. I…
The challenge of measuring intra-individual change in fatigue during cancer treatment
Validation of the PROMIS physical function measures in a diverse US population-based cohort of cancer patients
The Role of Technical Advances in the Adoption and Integration of Patient-reported Outcomes in Clinical Care
BACKGROUND: Patient-reported outcomes (PROs) are gaining recognition as key measures for improving the quality of patient care in clinical care settings. Three factors have made the implementation of PROs in clinical care more feasible: increased use of modern measurement methods in PRO design and validation, rapid progression of technology (eg, touchscreen tablets, Internet accessibility, and electronic health records), and greater demand for me…
Engaging Latina cancer survivors, their caregivers, and community partners in a randomized controlled trial
Patient-reported Outcomes (PROs)
Patient-centered outcomes research (PCOR) aims to improve care quality and patient outcomes by providing information that patients, clinicians, and family members need regarding treatment alternatives, and emphasizing patient input to inform the research process. PCOR capitalizes on available data sources and generates new evidence to provide timely and relevant information and can be conducted using prospective data collection, disease registrie…
A computerized adaptive version of the SF-36 is feasible for clinic and Internet administration in adults with HIV
DYNHA SF-36 is a computerized adaptive test version of the SF-36 Health Survey. The feasibility of administering a modified DYNHA SF-36 to adults with HIV was evaluated with Johns Hopkins University Moore (HIV) Clinic patients (N=100) and Internet consumer health panel members (N=101). Participants completed the DYNHA SF-36, modified to capture seven health domains [(physical function (PF), role function (RF, without physical or emotional attribu…
Relevant content for a patient-reported outcomes questionnaire for use in oncology clinical practice
PatientViewpoint
Gender and Racial Disparities in the Management of Diabetes Mellitus Among Medicare Patients
Sem obras proeminentes nesta página.
Gender and Racial Disparities in the Management of Diabetes Mellitus Among Medicare Patients
PatientViewpoint
Relevant content for a patient-reported outcomes questionnaire for use in oncology clinical practice
A computerized adaptive version of the SF-36 is feasible for clinic and Internet administration in adults with HIV
DYNHA SF-36 is a computerized adaptive test version of the SF-36 Health Survey. The feasibility of administering a modified DYNHA SF-36 to adults with HIV was evaluated with Johns Hopkins University Moore (HIV) Clinic patients (N=100) and Internet consumer health panel members (N=101). Participants completed the DYNHA SF-36, modified to capture seven health domains [(physical function (PF), role function (RF, without physical or emotional attribu…
Patient-reported Outcomes (PROs)
Patient-centered outcomes research (PCOR) aims to improve care quality and patient outcomes by providing information that patients, clinicians, and family members need regarding treatment alternatives, and emphasizing patient input to inform the research process. PCOR capitalizes on available data sources and generates new evidence to provide timely and relevant information and can be conducted using prospective data collection, disease registrie…
Engaging Latina cancer survivors, their caregivers, and community partners in a randomized controlled trial
Validation of the PROMIS physical function measures in a diverse US population-based cohort of cancer patients
The Role of Technical Advances in the Adoption and Integration of Patient-reported Outcomes in Clinical Care
BACKGROUND: Patient-reported outcomes (PROs) are gaining recognition as key measures for improving the quality of patient care in clinical care settings. Three factors have made the implementation of PROs in clinical care more feasible: increased use of modern measurement methods in PRO design and validation, rapid progression of technology (eg, touchscreen tablets, Internet accessibility, and electronic health records), and greater demand for me…
The challenge of measuring intra-individual change in fatigue during cancer treatment
Applying PRO Reference Values to Communicate Clinically Relevant Information at the Point-of-care
INTRODUCTION: The inclusion of reference values for common patient-reported outcomes (PROs) measures in clinical care settings provides a clinically relevant context for an individual patient's PRO scores. PRO reference values are currently not reported in clinical care settings. This is a missed opportunity, as clinicians are familiar with the presence and interpretation of reference values, commonly provided alongside laboratory test results. I…
Examination of individual and multiple comorbid conditions and health-related quality of life in older cancer survivors
Salivary, lacrimal and nasal (Salans) measure to assess side effects following radioactive iodine treatment
Medicine (12 obras) · Cancer survivorship and care (8 obras) · Computer Science (5 obras) · Gerontology (4 obras) · Internal Medicine (4 obras) · Nursing (4 obras) · Physical therapy (4 obras) · Population (4 obras) · Psychometrics (4 obras) · Childhood Cancer Survivors' Quality of Life (3 obras)