Uitgave 3/2016
Special section: Patient-reported Outcomes in Non-Standard Settings
Inhoudsopgave (26 Artikelen)
Introduction to special section on patient-reported outcomes in nonstandard settings
Carolyn E. Schwartz, Dennis A. Revicki
Ambulatory and diary methods can facilitate the measurement of patient-reported outcomes
Stefan Schneider, Arthur A. Stone
Advantages and psychometric validation of proximal intensive assessments of patient-reported outcomes collected in daily life
Eve B. Carlson, Nigel P. Field, Josef I. Ruzek, Richard A. Bryant, Constance J. Dalenberg, Terrence M. Keane, David A. Spain
Use of weekly assessment data to enhance evaluation of a subjective wellbeing intervention
Lucia Colla, Matthew Fuller-Tyszkiewicz, Adrian J. Tomyn, Ben Richardson, Justin D. Tomyn
AmbuFlex: tele-patient-reported outcomes (telePRO) as the basis for follow-up in chronic and malignant diseases
Liv Marit Valen Schougaard, Louise Pape Larsen, Anne Jessen, Per Sidenius, Liv Dorflinger, Annette de Thurah, Niels Henrik Hjollund
Evaluation of pedometry as a patient-centered outcome in patients undergoing hematopoietic cell transplant (HCT): a comparison of pedometry and patient reports of symptoms, health, and quality of life
Antonia V. Bennett, Bryce B. Reeve, Ethan M. Basch, Sandra A. Mitchell, Mathew Meeneghan, Claudio L. Battaglini, Abbie E. Smith-Ryan, Brett Phillips, Thomas C. Shea, William A. Wood
Symptom clusters in women with breast cancer: an analysis of data from social media and a research study
Sarah A. Marshall, Christopher C. Yang, Qing Ping, Mengnan Zhao, Nancy E. Avis, Edward H. Ip
Mode of administration does not cause bias in patient-reported outcome results: a meta-analysis
Claudia Rutherford, Daniel Costa, Rebecca Mercieca-Bebber, Holly Rice, Liam Gabb, Madeleine King
Evaluation of point-of-care PRO assessment in clinic settings: integration, parallel-forms reliability, and patient acceptability of electronic QOL measures during clinic visits
Pranav Sharma, Rodney L. Dunn, John T. Wei, James E. Montie, Scott M. Gilbert
Implementation of the Kids-CAT in clinical settings: a newly developed computer-adaptive test to facilitate the assessment of patient-reported outcomes of children and adolescents in clinical practice in Germany
D. Barthel, K. I. Fischer, S. Nolte, C. Otto, A. -K. Meyrose, S. Reisinger, M. Dabs, U. Thyen, M. Klein, H. Muehlan, T. Ankermann, O. Walter, M. Rose, U. Ravens-Sieberer
Patients’ and health professionals’ understanding of and preferences for graphical presentation styles for individual-level EORTC QLQ-C30 scores
W. Kuijpers, J. M. Giesinger, A. Zabernigg, T. Young, E. Friend, I. M. Tomaszewska, N. K. Aaronson, B. Holzner
Evaluating a new methodology for providing individualized feedback in healthcare on quality of life and its importance, using the WHOQOL-BREF in a community population
Alison M. Llewellyn, Suzanne M. Skevington
Evaluating PROMIS® instruments and methods for patient-centered outcomes research: Patient and provider voices in a substance use treatment setting
Kelly L. Johnston, Suzanne M. Lawrence, Nathan E. Dodds, Lan Yu, Dennis C. Daley, Paul A. Pilkonis
QLU-C10D: a health state classification system for a multi-attribute utility measure based on the EORTC QLQ-C30
M. T. King, D. S. J. Costa, N. K. Aaronson, J. E. Brazier, D. F. Cella, P. M. Fayers, P. Grimison, M. Janda, G. Kemmler, R. Norman, A. S. Pickard, D. Rowen, G. Velikova, T. A. Young, R. Viney
Using a discrete choice experiment to value the QLU-C10D: feasibility and sensitivity to presentation format
R. Norman, R. Viney, N. K. Aaronson, J. E. Brazier, D. Cella, D. S. J. Costa, P. M. Fayers, G. Kemmler, S. Peacock, A. S. Pickard, D. Rowen, D. J. Street, G. Velikova, T. A. Young, M. T. King
Health-related needs of people with multiple chronic diseases: differences and underlying factors
Petra Hopman, François G. Schellevis, Mieke Rijken
The effectiveness of a preventive health program and vitamin D status in improving health-related quality of life of older Canadians
J. P. Ekwaru, A. Ohinmaa, Paul J. Veugelers
Smoking status and health-related quality of life: a longitudinal study in young adults
Jing Tian, Alison J. Venn, Leigh Blizzard, George C. Patton, Terry Dwyer, Seana L. Gall
Impact of Alzheimer’s disease on the family caregiver’s long-term quality of life: results from an ALSOVA follow-up study
Tarja H. Välimäki, Janne A. Martikainen, Kristiina Hongisto, Saku Väätäinen, Harri Sintonen, Anne M. Koivisto
Well-being and environmental quality: Does pollution affect life satisfaction?
Kati Orru, Hans Orru, Marek Maasikmets, Reigo Hendrikson, Mare Ainsaar
Japanese population norms for preference-based measures: EQ-5D-3L, EQ-5D-5L, and SF-6D
Takeru Shiroiwa, Takashi Fukuda, Shunya Ikeda, Ataru Igarashi, Shinichi Noto, Shinya Saito, Kojiro Shimozuma
The development of a questionnaire measure of diabetes-related distress in Chinese-speaking patients: the Diabetes-Related Distress Questionnaire (DRDQ)
Huey-Fen Wang, Neng-Chun Yu, Wayne H-H Sheu, Mei Chang Yeh
Dimensionality of the Center for Epidemiologic Studies Depression Scale: an exploratory bi-factor analytic study
Ted C. T. Fong, Cecilia L. W. Chan, Rainbow T. H. Ho, Jessie S. M. Chan, Celia H. Y. Chan, S. M. Ng
Concurrent validity of the PROMIS® pediatric global health measure
Christopher B. Forrest, Carole A. Tucker, Ulrike Ravens-Sieberer, Ramya Pratiwadi, JeanHee Moon, Rachel E. Teneralli, Brandon Becker, Katherine B. Bevans
Stability of the 13-item sense of coherence (SOC) scale: a longitudinal prospective study in women treated for breast cancer
Carina Lindblad, Kerstin Sandelin, Lena-Marie Petersson, Camelia Rohani, Ann Langius-Eklöf
Dutch–Flemish translation of nine pediatric item banks from the Patient-Reported Outcomes Measurement Information System (PROMIS)®
Lotte Haverman, Martha A. Grootenhuis, Hein Raat, Marion A. J. van Rossum, Eline van Dulmen-den Broeder, Karel Hoppenbrouwers, Helena Correia, David Cella, Leo D. Roorda, Caroline B. Terwee