Quality of Life Research 3/2016

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Inhoudsopgave ( 26 Artikelen )

01-03-2016 | Editorial | Uitgave 3/2016

Introduction to special section on patient-reported outcomes in nonstandard settings

Carolyn E. Schwartz, Dennis A. Revicki

23-06-2015 | Uitgave 3/2016

Ambulatory and diary methods can facilitate the measurement of patient-reported outcomes

Stefan Schneider, Arthur A. Stone

01-03-2016 | Special Section: PROs in Non-Standard Settings (by invitation only) | Uitgave 3/2016

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

01-03-2016 | Special Section: PROs in Non-Standard Settings (by invitation only) | Uitgave 3/2016

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

01-03-2016 | Special Section: PROs in Non-Standard Settings (by invitation only) | Uitgave 3/2016 Open Access

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

Naar de volledige tekst

01-03-2016 | Special Section: PROs in Non-Standard Settings (by invitation only) | Uitgave 3/2016

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

01-03-2016 | Special Section: PROs in Non-Standard Settings (by invitation only) | Uitgave 3/2016

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

03-09-2015 | Special Section: PROs in Non-Standard Settings (by invitation only) | Uitgave 3/2016

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

01-03-2016 | Special Section: PROs in Non-Standard Settings (by invitation only) | Uitgave 3/2016

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

01-03-2016 | Special Section: PROs in Non-Standard Settings (by invitation only) | Uitgave 3/2016

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

09-09-2015 | Special Section: PROs in Non-Standard Settings (by invitation only) | Uitgave 3/2016 Open Access

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

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14-09-2015 | Special Section: PROs in Non-Standard Settings (by invitation only) | Uitgave 3/2016

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

09-09-2015 | Special Section: PROs in Non-Standard Settings (by invitation only) | Uitgave 3/2016

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

01-03-2016 | Uitgave 3/2016

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

05-09-2015 | Uitgave 3/2016

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

04-09-2015 | Uitgave 3/2016

Health-related needs of people with multiple chronic diseases: differences and underlying factors

Petra Hopman, François G. Schellevis, Mieke Rijken

18-08-2015 | Original Paper | Uitgave 3/2016 Open Access

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

Naar de volledige tekst

27-08-2015 | Uitgave 3/2016

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

09-09-2015 | Uitgave 3/2016

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

20-08-2015 | Brief Communication | Uitgave 3/2016

Well-being and environmental quality: Does pollution affect life satisfaction?

Kati Orru, Hans Orru, Marek Maasikmets, Reigo Hendrikson, Mare Ainsaar

25-08-2015 | Uitgave 3/2016 Open Access

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

Naar de volledige tekst

22-08-2015 | Uitgave 3/2016

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

18-08-2015 | Uitgave 3/2016 Open Access

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

Naar de volledige tekst

27-08-2015 | Uitgave 3/2016

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

29-08-2015 | Uitgave 3/2016

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

28-03-2015 | Brief Communication | Uitgave 3/2016 Open Access

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

Naar de volledige tekst

Quality of Life Research

Uitgave 3/2016

Inhoudsopgave ( 26 Artikelen )

Introduction to special section on patient-reported outcomes in nonstandard settings

Ambulatory and diary methods can facilitate the measurement of patient-reported outcomes

Advantages and psychometric validation of proximal intensive assessments of patient-reported outcomes collected in daily life

Use of weekly assessment data to enhance evaluation of a subjective wellbeing intervention

AmbuFlex: tele-patient-reported outcomes (telePRO) as the basis for follow-up in chronic and malignant diseases

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

Symptom clusters in women with breast cancer: an analysis of data from social media and a research study

Mode of administration does not cause bias in patient-reported outcome results: a meta-analysis

Evaluation of point-of-care PRO assessment in clinic settings: integration, parallel-forms reliability, and patient acceptability of electronic QOL measures during clinic visits

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

Patients’ and health professionals’ understanding of and preferences for graphical presentation styles for individual-level EORTC QLQ-C30 scores

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

Evaluating PROMIS® instruments and methods for patient-centered outcomes research: Patient and provider voices in a substance use treatment setting

QLU-C10D: a health state classification system for a multi-attribute utility measure based on the EORTC QLQ-C30

Using a discrete choice experiment to value the QLU-C10D: feasibility and sensitivity to presentation format

Health-related needs of people with multiple chronic diseases: differences and underlying factors

The effectiveness of a preventive health program and vitamin D status in improving health-related quality of life of older Canadians

Smoking status and health-related quality of life: a longitudinal study in young adults

Impact of Alzheimer’s disease on the family caregiver’s long-term quality of life: results from an ALSOVA follow-up study

Well-being and environmental quality: Does pollution affect life satisfaction?

Japanese population norms for preference-based measures: EQ-5D-3L, EQ-5D-5L, and SF-6D

The development of a questionnaire measure of diabetes-related distress in Chinese-speaking patients: the Diabetes-Related Distress Questionnaire (DRDQ)

Dimensionality of the Center for Epidemiologic Studies Depression Scale: an exploratory bi-factor analytic study

Concurrent validity of the PROMIS® pediatric global health measure

Stability of the 13-item sense of coherence (SOC) scale: a longitudinal prospective study in women treated for breast cancer

Dutch–Flemish translation of nine pediatric item banks from the Patient-Reported Outcomes Measurement Information System (PROMIS)®

Uitgave 9/2020

Uitgave 8/2020

Uitgave 7/2020

Uitgave 6/2020

Uitgave 5/2020

Uitgave 4/2020

Uitgave 3/2020

Uitgave 2/2020

Uitgave 1/2020

Uitgave 12/2019

Bohn Stafleu van Loghum

Inhoudsopgave ( 26 Artikelen )

Introduction to special section on patient-reported outcomes in nonstandard settings

Ambulatory and diary methods can facilitate the measurement of patient-reported outcomes

Advantages and psychometric validation of proximal intensive assessments of patient-reported outcomes collected in daily life

Use of weekly assessment data to enhance evaluation of a subjective wellbeing intervention

AmbuFlex: tele-patient-reported outcomes (telePRO) as the basis for follow-up in chronic and malignant diseases

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

Symptom clusters in women with breast cancer: an analysis of data from social media and a research study

Mode of administration does not cause bias in patient-reported outcome results: a meta-analysis

Evaluation of point-of-care PRO assessment in clinic settings: integration, parallel-forms reliability, and patient acceptability of electronic QOL measures during clinic visits

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

Patients’ and health professionals’ understanding of and preferences for graphical presentation styles for individual-level EORTC QLQ-C30 scores

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

Evaluating PROMIS® instruments and methods for patient-centered outcomes research: Patient and provider voices in a substance use treatment setting

QLU-C10D: a health state classification system for a multi-attribute utility measure based on the EORTC QLQ-C30

Using a discrete choice experiment to value the QLU-C10D: feasibility and sensitivity to presentation format

Health-related needs of people with multiple chronic diseases: differences and underlying factors

The effectiveness of a preventive health program and vitamin D status in improving health-related quality of life of older Canadians

Smoking status and health-related quality of life: a longitudinal study in young adults

Impact of Alzheimer’s disease on the family caregiver’s long-term quality of life: results from an ALSOVA follow-up study

Well-being and environmental quality: Does pollution affect life satisfaction?

Japanese population norms for preference-based measures: EQ-5D-3L, EQ-5D-5L, and SF-6D

The development of a questionnaire measure of diabetes-related distress in Chinese-speaking patients: the Diabetes-Related Distress Questionnaire (DRDQ)

Dimensionality of the Center for Epidemiologic Studies Depression Scale: an exploratory bi-factor analytic study

Concurrent validity of the PROMIS® pediatric global health measure

Stability of the 13-item sense of coherence (SOC) scale: a longitudinal prospective study in women treated for breast cancer

Dutch–Flemish translation of nine pediatric item banks from the Patient-Reported Outcomes Measurement Information System (PROMIS)®

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