Skip to main content

ETHNOS_APP

Home • Search • Journals • List 0

Charles S Cleeland

Biographic Data

ID5542310
NAMECharles S Cleeland
GIVEN NAMESCharles S
FAMILY NAMECleeland
SIGNATURECLEELAND C S
AFFILIATIONSThe University of Texas MD Anderson Cancer Center
ORCID0000-0002-1460-6527
VERIFIEDYes
TOTAL WORKS10
TOTAL CITATIONS0
AUTHOR COUNT10
EDITOR COUNT0
FIRST PUBLICATION YEAR1970
LATEST PUBLICATION YEAR2025
H-INDEX0
  • Defining critical symptom parameters for an ePRO-based management pathway during systemic treatment for advanced upper gastrointestinal cancer: A longitudinal study

    Open Access•Xin Shelley Wang, M Murphy et al.•ARTICLE•Quality of Life Research•2025

  • Interpreting Patient-reported Outcome Scores for Clinical Research and Practice: Definition, Determination, and Application of Cutpoints

    Qiuling Shi, Tito R Mendoza et al.•ARTICLE•Medical Care•2019•References: 42

    OBJECTIVES: Cutpoints are specific numeric values used to create discrete categories for patient-reported outcome (PRO) items or scales. Cutpoints are widely used in both clinical research and practice. This article offers a definition for cutpoints, describes strategies for determining actionable cutpoints, and discusses considerations related to interpreting cutpoints in clinical applications. METHODS: We clarify the definition of cutpoints for…

  • Patient-reported lung symptoms as an early signal of impending radiation pneumonitis in patients with non-small cell lung cancer treated with chemoradiation: An observational study

    Open Access•Jinbo Yue, Qiuling Shi et al.•ARTICLE•Quality of Life Research•2018

  • An exploration of differences between Japan and two European countries in the self-reporting and valuation of pain and discomfort on the EQ-5D

    Open Access•Yan Feng, Mike Herdman et al.•ARTICLE•Quality of Life Research•2017

    This study provides evidence of between-country differences in the self-reporting and valuation of health, including pain/discomfort, when using EQ-5D in general population samples. The results suggest a need for caution when comparing or aggregating EQ-5D self-reported data in multi-country studies

  • Utility of a patient-reported outcome in measuring functional impairment during autologous stem cell transplant in patients with multiple myeloma

    Open Access•Nina Shah, Qiuling Shi et al.•ARTICLE•Quality of Life Research•2017

  • The utility of patient-reported outcome measures among patients with myalgic encephalomyelitis/chronic fatigue syndrome

    Open Access•Kyle W Murdock, Xin Shelley Wang et al.•ARTICLE•Quality of Life Research•2016

  • Using group-based trajectory modeling to examine heterogeneity of symptom burden in patients with head and neck cancer undergoing aggressive non-surgical therapy

    Open Access•Qiuling Shi, Tito R Mendoza et al.•ARTICLE•Quality of Life Research•2013

  • Prognostic value of patient-reported symptom interference in patients with late-stage lung cancer

    Open Access•Bradley J Barney, Xin Shelley Wang et al.•ARTICLE•Quality of Life Research•2013

  • The Association between Symptom Burdens and Utility in Chinese Cancer Patients

    Open Access•Ya-Chen Tina Shih, Xin Shelley Wang et al.•ARTICLE•Quality of Life Research•2006

  • MMPI Profiles in Exacerbation and Remission of Multiple Sclerosis

    Open Access•Charles S Cleeland, Charles G Matthews et al.•ARTICLE•Psychological Reports•1970

    Profile analysis of MMPI profiles generated by 30 patients displaying exacerbation (E) or remission (R) of the symptoms of multiple sclerosis is reported. Profiles classified as “abnormal” were significantly more frequent in the E group. Significantly more E patients had elevations on D greater than 70. The ordering of elevations of the clinical scales was similar in both groups

No prominent works on this page.

  • MMPI Profiles in Exacerbation and Remission of Multiple Sclerosis

    Open Access•Charles S Cleeland, Charles G Matthews et al.•ARTICLE•Psychological Reports•1970

    Profile analysis of MMPI profiles generated by 30 patients displaying exacerbation (E) or remission (R) of the symptoms of multiple sclerosis is reported. Profiles classified as “abnormal” were significantly more frequent in the E group. Significantly more E patients had elevations on D greater than 70. The ordering of elevations of the clinical scales was similar in both groups

  • The Association between Symptom Burdens and Utility in Chinese Cancer Patients

    Open Access•Ya-Chen Tina Shih, Xin Shelley Wang et al.•ARTICLE•Quality of Life Research•2006

  • Using group-based trajectory modeling to examine heterogeneity of symptom burden in patients with head and neck cancer undergoing aggressive non-surgical therapy

    Open Access•Qiuling Shi, Tito R Mendoza et al.•ARTICLE•Quality of Life Research•2013

  • Prognostic value of patient-reported symptom interference in patients with late-stage lung cancer

    Open Access•Bradley J Barney, Xin Shelley Wang et al.•ARTICLE•Quality of Life Research•2013

  • The utility of patient-reported outcome measures among patients with myalgic encephalomyelitis/chronic fatigue syndrome

    Open Access•Kyle W Murdock, Xin Shelley Wang et al.•ARTICLE•Quality of Life Research•2016

  • An exploration of differences between Japan and two European countries in the self-reporting and valuation of pain and discomfort on the EQ-5D

    Open Access•Yan Feng, Mike Herdman et al.•ARTICLE•Quality of Life Research•2017

    This study provides evidence of between-country differences in the self-reporting and valuation of health, including pain/discomfort, when using EQ-5D in general population samples. The results suggest a need for caution when comparing or aggregating EQ-5D self-reported data in multi-country studies

  • Utility of a patient-reported outcome in measuring functional impairment during autologous stem cell transplant in patients with multiple myeloma

    Open Access•Nina Shah, Qiuling Shi et al.•ARTICLE•Quality of Life Research•2017

  • Patient-reported lung symptoms as an early signal of impending radiation pneumonitis in patients with non-small cell lung cancer treated with chemoradiation: An observational study

    Open Access•Jinbo Yue, Qiuling Shi et al.•ARTICLE•Quality of Life Research•2018

  • Interpreting Patient-reported Outcome Scores for Clinical Research and Practice: Definition, Determination, and Application of Cutpoints

    Qiuling Shi, Tito R Mendoza et al.•ARTICLE•Medical Care•2019•References: 42

    OBJECTIVES: Cutpoints are specific numeric values used to create discrete categories for patient-reported outcome (PRO) items or scales. Cutpoints are widely used in both clinical research and practice. This article offers a definition for cutpoints, describes strategies for determining actionable cutpoints, and discusses considerations related to interpreting cutpoints in clinical applications. METHODS: We clarify the definition of cutpoints for…

  • Defining critical symptom parameters for an ePRO-based management pathway during systemic treatment for advanced upper gastrointestinal cancer: A longitudinal study

    Open Access•Xin Shelley Wang, M Murphy et al.•ARTICLE•Quality of Life Research•2025

Medicine (9 works) · Internal Medicine (7 works) · Cancer survivorship and care (6 works) · Physical therapy (5 works) · Psychology (4 works) · Quality of life (healthcare (4 works) · Clinical Psychology (3 works) · Clinical Psychology (3 works) · Head and Neck Cancer Studies (3 works) · Cancer (2 works)

Ethnos_APP • Open Source Project • MIT License • Frontend v2.0.0 • Privacy and Cookies • API Documentation: api.ethnos.app/docs • API Source Code: GitHub • DOI: 10.5281/zenodo.17049435 • Frontend Source Code: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae