Bryce B Reeve
Biographic Data
| ID | 184755 |
|---|---|
| NAME | Bryce B Reeve |
| GIVEN NAMES | Bryce B |
| FAMILY NAME | Reeve |
| SIGNATURE | REEVE B B |
| AFFILIATIONS | University of North Carolina at Chapel Hill |
| ORCID | 0000-0002-6709-8714 |
| VERIFIED | Yes |
| TOTAL WORKS | 61 |
| TOTAL CITATIONS | 104 |
| AUTHOR COUNT | 61 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2005 |
| LATEST PUBLICATION YEAR | 2026 |
| H-INDEX | 3 |
The spectrum of communication abilities in children with 12 rare neurodevelopmental disorders: A qualitative study with caregivers
BACKGROUND: Our aim was to update an existing model of communication ability for children with rare neurodevelopmental disorders (NDDs) by centring caregiver and family perspectives. This project is part of a larger initiative to improve the measurement of communication ability for these children in the context of clinical trials. METHODS: We conducted concept elicitation interviews with purposively selected clinical experts and caregivers of chi…
Developing an Index to Measure Structural Racism: Methodological Process, Challenges, and Considerations
Access to valid and reliable measures of structural racism is essential for addressing health inequities, yet few validated ecological-level indices exist for assessing structural racism affecting Black and Hispanic populations in the United States. Guided by the National Institute on Minority Health and Health Disparities framework, our interdisciplinary team undertook the development of an ecological-level structural racism index. In the proces…
Identifying High-Priority Ecological-Level Indicators of Structural Racism in Black and Hispanic/Latino Communities
Structural racism manifests as a multifaceted phenomenon in which various social and structural drivers of health can carry different levels of significance and impact. This study used a theory-driven approach to identify high-priority key ecological-level manifestations of structural racism to inform the development of a novel, multilevel, and multidimensional structural racism measure for Black and Hispanic/Latino communities. Based on the Nati…
Cosmin reporting guideline for studies on measurement properties of patient‐reported outcome measures: Version 2.0
Comparison of patient-reported symptoms with multi-item patient-reported outcome measures of fatigue, anxiety, and depression in the clinical care of women undergoing chemotherapy for early breast can…
Recalling what we thought we knew about recall periods: A qualitative descriptive study of how adults diagnosed with cancer use recall periods for patient-reported outcome items about physical functio…
Including a 7-day recall period improves recall consistency for patients when answering physical function PROM items, but there is still room for improvement. The inaccuracy of recall for PROMs in clinical trials influences the ability to calculate the change in treatment outcomes over time and may conceal or emphasize actual treatment effects
What facets of physical function are most important to adults diagnosed with cancer
Evaluating anchor variables and variation in meaningful score differences for PROMIS® Pediatric measures in children and adolescents living with a rheumatic disease
Many of the candidate external anchoring variables did not meet pre-specified criteria for calculating MSDs. Even for those that did, the choice of anchoring variable had a strong impact on the estimated MSD value and were different from other published values. As in adults, establishing pediatric MSDs requires selection of high-quality anchors, as changes in the variables used as anchors can impact MSD values and any subsequent score interpretat…
Health-related quality of life profiles of adults with arthritis and/or fibromyalgia: A cross-sectional study
We identified profiles with consistently impacted HRQOL in arthritis, though one displayed average mental health functioning despite poor physical functioning. These results highlight the value of considering the patient's HRQOL experience alongside treatment options, and the potentially positive impact of non-pharmacological interventions
The Fact-GP5 as a global tolerability measure: Responsiveness and robustness to missing assessments
2003
Development of an ultra-short measure of eight domains of health-related quality of life for research and clinical care: The patient-reported outcomes measurement information system® PROMIS®-16 profil…
The PROMIS-16 Profile provides an attractive brief measure of eight distinct domains of health-related quality of life, representing an ideal screening tool for clinical care, which can help clinicians quickly identify distinct areas of concern that may require further assessment and follow-up. Further research is needed to confirm and extend these findings
Health-related quality of life profiles in adolescents and young adults with chronic conditions
Investigating gender-based differential item functioning on the Kansas City Cardiomyopathy Questionnaire (KCCQ) using qualitative content analysis
Identifying clinically meaningful severity categories for PROMIS pediatric measures of anxiety, mobility, fatigue, and depressive symptoms in juvenile idiopathic arthritis and childhood-onset systemic…
Racial differences in user experiences and perceived value of electronic symptom monitoring in a cohort of black and white bladder and prostate cancer patients
The association of age, literacy, and race on completing patient-reported outcome measures in pediatric oncology
PRO-Bookmarking to Estimate Clinical Thresholds for Patient-reported Symptoms and Function
INTRODUCTION: PRO-Bookmarking is an alternative to traditional methods for deriving cut scores and applying qualitative modifiers to score ranges. METHODS: In PRO-Bookmarking, a working group of stakeholders identifies ranges of scores they judge to credibly define different levels of a patient-reported outcome (PRO). Subsets of items and responses, called "clinical vignettes," are woven into a narrative to represent different levels of the PRO. …
Determining a transitional scoring link between PROMIS® pediatric and adult physical health measures
Assessing responsiveness over time of the PROMIS® pediatric symptom and function measures in cancer, nephrotic syndrome, and sickle cell disease
The prognostic value of pre-diagnosis health-related quality of life on survival: A prospective cohort study of older Americans with lung cancer
Examining health-related quality of life patterns in women with breast cancer
Evaluating measurement invariance across assessment modes of phone interview and computer self-administered survey for the PROMIS measures in a population-based cohort of localized prostate cancer sur…
Use of the SF-36v2 Health Survey as a Screen for Risk of Major Depressive Disorder in a US Population-based Sample and Subgroup With Chronic Pain
STUDY OBJECTIVES: To assess the feasibility of using the SF-36v2 mental health (MH) and mental component summary (MCS) scores for classification of risk for major depressive disorder (MDD), and to determine cut-off scores based on the sensitivity and specificity in a general US representative sample, and a chronic pain subpopulation. METHODS: Data were analyzed from the 2013 US National Health and Wellness Survey (adults 18 y old and above; N=75,…
Sexual Satisfaction and the Importance of Sexual Health to Quality of Life Throughout the Life Course of U.S. Adults
An item-level response shift study on the change of health state with the rating of asthma-specific quality of life: A report from the PROMIS® Pediatric Asthma Study
Measuring Everyday Racial/Ethnic Discrimination in Health Surveys: How Best to Ask the Questions, in One or Two Stages, Across Multiple Racial/Ethnic Groups
While it is clear that self-reported racial/ethnic discrimination is related to illness, there are challenges in measuring self-reported discrimination or unfair treatment. In the present study, we evaluate the psychometric properties of a self-reported instrument across racial/ethnic groups in a population-based sample, and we test and interpret findings from applying two different widely-used approaches to asking about discrimination and unfair…
Comparing Cognitive Interviewing and Psychometric Methods to Evaluate a Racial/Ethnic Discrimination Scale
Proponents of survey evaluation have long advocated the integration of qualitative and quantitative methodologies, but this recommendation has rarely been practiced. The authors used both methods to evaluate the "Everyday Discrimination" scale (EDS), which measures frequency of various types of discrimination, in a multiethnic population. Cognitive testing included 30 participants of various race/ethnic backgrounds and identified items that were …
Posttraumatic Growth and Health-related Quality of Life in a Racially Diverse Cohort of Breast Cancer Survivors
This study examined the relationship between race, religiosity, and posttraumatic growth as well as the association between growth and physical and mental health-related quality of life (HRQOL) in breast cancer survivors ( N = 802; M age = 57.2). Multivariate analyses revealed that African American breast cancer survivors reported higher levels of posttraumatic growth than White women. However, this relationship was mediated by religiosity. We fo…
Sources of Interactional Problems in a Survey of Racial/Ethnic Discrimination
Cross-cultural variability in respondent processing of survey questions may bias results from multiethnic samples. We analyzed behavior codes, which identify difficulties in the interactions of respondents and interviewers, from a discrimination module contained within a field test of the 2007 California Health Interview Survey. In all, 553 (English) telephone interviews yielded 13,999 interactions involving 22 items. Multilevel logistic regressi…
Do Patients Consistently Report Comorbid Conditions Over Time: Results From the Prostate Cancer Outcomes Study
BACKGROUND: Comorbidity is an important dimension of patient health status. However, limited attention has been given to assessing the reliability of patient-reported data on comorbid conditions. OBJECTIVES: We sought to evaluate the consistency of self-report of 12 comorbid conditions at 3 distinct time points and examine the sociodemographic, clinical, health status, and survey factors associated with reliability. STUDY DESIGN: We undertook a l…
Special Issues for Building Computerized-Adaptive Tests for Measuring Patient-Reported Outcomes: The National Institute of Health??s Investment in New Technology
From the National Cancer Institute, National Institutes of Health, Bethesda, Maryland. This article was written by an author in his capacity as an NCI employee, but the views expressed in this paper do not necessarily represent those of the NCI or NIH. Reprints: Bryce B. Reeve, PhD, Outcomes Research Branch, Applied Research Program, Division of Cancer Control and Population Sciences, National Cancer Institute, National Institutes of Health, 6130…
Methodological issues for building item banks and computerized adaptive scales
Applying item response theory (IRT) modeling to questionnaire development, evaluation, and refinement
Developing tailored instruments: Item banking and computerized adaptive assessment
Applying item response theory to enhance health outcomes assessment
IRT health outcomes data analysis project: An overview and summary
Fatigue in breast cancer survivors two to five years post diagnosis: A Heal Study report
Enhancing measurement in health outcomes research supported by Agencies within the US Department of Health and Human Services
The Patient-Reported Outcomes Measurement Information System (PROMIS): Progress of an NIH Roadmap Cooperative Group During its First Two Years
The NIH PROMIS network derived a consensus-based framework for self-reported health, systematically reviewed available instruments and datasets that address the initial PROMIS domains. Qualitative item research led to the first wave of network testing which began in the second year
Psychometric Evaluation and Calibration of Health-Related Quality of Life Item Banks: Plans for the Patient-Reported Outcomes Measurement Information System (PROMIS)
BACKGROUND: The construction and evaluation of item banks to measure unidimensional constructs of health-related quality of life (HRQOL) is a fundamental objective of the Patient-Reported Outcomes Measurement Information System (PROMIS) project. OBJECTIVES: Item banks will be used as the foundation for developing short-form instruments and enabling computerized adaptive testing. The PROMIS Steering Committee selected 5 HRQOL domains for initial f…
Using cognitive interviews to evaluate items for measuring sexual functioning across cancer populations: Improvements and remaining challenges
The Patient-Reported Outcomes Measurement Information System (PROMIS) developed and tested its first wave of adult self-reported health outcome item banks: 2005–2008
Posttraumatic Growth and Health-related Quality of Life in a Racially Diverse Cohort of Breast Cancer Survivors
This study examined the relationship between race, religiosity, and posttraumatic growth as well as the association between growth and physical and mental health-related quality of life (HRQOL) in breast cancer survivors ( N = 802; M age = 57.2). Multivariate analyses revealed that African American breast cancer survivors reported higher levels of posttraumatic growth than White women. However, this relationship was mediated by religiosity. We fo…
Comparing Cognitive Interviewing and Psychometric Methods to Evaluate a Racial/Ethnic Discrimination Scale
Proponents of survey evaluation have long advocated the integration of qualitative and quantitative methodologies, but this recommendation has rarely been practiced. The authors used both methods to evaluate the "Everyday Discrimination" scale (EDS), which measures frequency of various types of discrimination, in a multiethnic population. Cognitive testing included 30 participants of various race/ethnic backgrounds and identified items that were …
Measuring Everyday Racial/Ethnic Discrimination in Health Surveys: How Best to Ask the Questions, in One or Two Stages, Across Multiple Racial/Ethnic Groups
While it is clear that self-reported racial/ethnic discrimination is related to illness, there are challenges in measuring self-reported discrimination or unfair treatment. In the present study, we evaluate the psychometric properties of a self-reported instrument across racial/ethnic groups in a population-based sample, and we test and interpret findings from applying two different widely-used approaches to asking about discrimination and unfair…
Attitudes and Intentions Regarding Abortion Provision Among Medical School Students in South Africa
CONTEXT: Although South Africa liberalized its abortion law in 1996, significant barriers still impede service provision, including the lack of trained and willing providers. A better understanding is needed of medical students' attitudes, beliefs and intentions regarding abortion provision. METHODS: Surveys about abortion attitudes, beliefs and practice intentions were conducted in 2005 and 2007 among 1,308 medical school students attending the …
Monitoring population health for Healthy People 2020: Evaluation of the NIH PROMIS® Global Health, CDC Healthy Days, and satisfaction with life instruments
The Use of Patient-reported Outcomes (PRO) Within Comparative Effectiveness Research: Implications for Clinical Practice and Health Care Policy
BACKGROUND: The goal of comparative effectiveness research (CER) is to explain the differential benefits and harms of alternate methods to prevent, diagnose, treat, and monitor a clinical condition or to improve the delivery of care. To inform decision making, information from the patient's perspective that reflects outcomes that patients care about are needed and can be collected rigorously using appropriate patient-reported outcomes (PRO). It c…
Initial Validation of a Self-Report Measure of the Extent of and Reasons for Medication Nonadherence
BACKGROUND: Self-report measures of medication nonadherence confound the extent of and reasons for medication nonadherence. Each construct is assessed with a different type of psychometric model, which dictates how to establish reliability and validity. OBJECTIVES: To evaluate the psychometric properties of a self-report measure of medication nonadherence that assesses separately the extent of nonadherence and reasons for nonadherence. RESEARCH D…
Isoqol recommends minimum standards for patient-reported outcome measures used in patient-centered outcomes and comparative effectiveness research
Associations of cancer and other chronic medical conditions with SF-6D preference-based scores in Medicare beneficiaries
Cognitive interviewing of the US National Cancer Institute’s Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)
Deriving clinically meaningful cut-scores for fatigue in a cohort of breast cancer survivors: A Health, Eating, Activity, and Lifestyle (Heal) Study
In Response
Institute for Clinical Evaluative Sciences Toronto, ON, Canada †Department of Epidemiology and Biostatistics, Michigan State University East Lansing, MI Supported by an operating grant from the Canadian Institutes of Health Research (CIHR). P.C.A. is also supported in part by a Career Investigator Award from the Heart and Stroke Foundation. The authors declare no conflict of interest
Medicine (53 works) · Psychology (35 works) · Clinical Psychology (29 works) · Clinical Psychology (25 works) · Internal Medicine (24 works) · Public health (24 works) · Quality of Life Research (21 works) · Cancer survivorship and care (20 works) · Gerontology (20 works) · Population (20 works)