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Mona L Martin

Biographic Data

ID7692918
NAMEMona L Martin
GIVEN NAMESMona L
FAMILY NAMEMartin
SIGNATUREMARTIN M L
AFFILIATIONSWilliams & Associates
ORCID0000-0001-6899-2139
VERIFIEDYes
TOTAL WORKS10
TOTAL CITATIONS0
AUTHOR COUNT10
EDITOR COUNT0
FIRST PUBLICATION YEAR1999
LATEST PUBLICATION YEAR2021
H-INDEX0
  • How patients being treated for non-small cell lung cancer value treatment benefit despite side effects

    Open Access•Mona L Martin, Julia R Correll et al.•ARTICLE•Quality of Life Research•2021

    In these two qualitative sub-studies, patients with advanced NSCLC valued the benefits of their treatment regardless of side effects that they experienced. Patients weighed their options against the seriousness of their disease and expressed their willingness to tolerate their side effects in return for receiving continued treatment benefits

  • Willingness to report treatment-related symptoms of immunotherapy among patients with non-small cell lung cancer

    Open Access•Mona L Martin, Helena Chung et al.•ARTICLE•Quality of Life Research•2021

    Patients have a range of reasons for not reporting their treatment-related symptoms when undergoing immunotherapy for NSCLC. Reasons are more strongly related to determination of the severity versus manageability of patients' experiences of symptoms than they are to the fear of having treatment discontinued

  • Content validity of the ASQoL for use in a non-radiographic axial spondyloarthritis population

    Open Access•Mark C Hwang, Mona L Martin et al.•ARTICLE•Quality of Life Research•2020

    Our results represent an important first step in confirming the relevance of the concepts in the ASQoL to patients with nr-axSpA, supporting quantitative assessment of ASQoL validity in this population

  • Qualitative development of the ‘Questionnaire on Pain caused by Spasticity (QPS),’ a pediatric patient‐reported outcome for spasticity‐related pain in cerebral palsy

    Open Access•Thorin L Geister, Manjari Quintanar-Solares et al.•ARTICLE•Quality of Life Research•2013

    The QPS is a novel instrument for the assessment of spasticity-related pain in children/adolescents with CP that was developed with direct patient input. Its modules allow the use of this instrument in children/adolescents with varied levels of impairment and communication skills

  • Equivalence and measurement properties of an electronic version of the Psoriasis Symptom Inventory

    Open Access•Donald M Bushnell, Mona L Martin et al.•ARTICLE•Quality of Life Research•2013

  • Content Validity—Establishing and Reporting the Evidence in Newly Developed Patient-Reported Outcomes (PRO) Instruments for Medical Product Evaluation

    Open Access•Donald L Patrick, Laurie B Burke et al.•ARTICLE•Value in Health•2011

  • Content Validity—Establishing and Reporting the Evidence in Newly Developed Patient-Reported Outcomes (PRO) Instruments for Medical Product Evaluation

    Open Access•Donald L Patrick, Laurie B Burke et al.•ARTICLE•Value in Health•2011

  • Content validation of two SF-36 subscales for use in type 2 diabetes and non-dialysis chronic kidney disease-related anemia

    Open Access•Mona L Martin, Donald L Patrick et al.•ARTICLE•Quality of Life Research•2010

  • Quality of Life of Women with Urinary Incontinence

    Open Access•Donald M Bushnell, Mona L Martin et al.•ARTICLE•Quality of Life Research•2005

  • Quality of life and parkinson's disease

    Open Access•Donald M Bushnell, Mona L Martin•ARTICLE•Quality of Life Research•1999

No prominent works on this page.

  • Quality of life and parkinson's disease

    Open Access•Donald M Bushnell, Mona L Martin•ARTICLE•Quality of Life Research•1999

  • Quality of Life of Women with Urinary Incontinence

    Open Access•Donald M Bushnell, Mona L Martin et al.•ARTICLE•Quality of Life Research•2005

  • Content validation of two SF-36 subscales for use in type 2 diabetes and non-dialysis chronic kidney disease-related anemia

    Open Access•Mona L Martin, Donald L Patrick et al.•ARTICLE•Quality of Life Research•2010

  • Content Validity—Establishing and Reporting the Evidence in Newly Developed Patient-Reported Outcomes (PRO) Instruments for Medical Product Evaluation

    Open Access•Donald L Patrick, Laurie B Burke et al.•ARTICLE•Value in Health•2011

  • Content Validity—Establishing and Reporting the Evidence in Newly Developed Patient-Reported Outcomes (PRO) Instruments for Medical Product Evaluation

    Open Access•Donald L Patrick, Laurie B Burke et al.•ARTICLE•Value in Health•2011

  • Qualitative development of the ‘Questionnaire on Pain caused by Spasticity (QPS),’ a pediatric patient‐reported outcome for spasticity‐related pain in cerebral palsy

    Open Access•Thorin L Geister, Manjari Quintanar-Solares et al.•ARTICLE•Quality of Life Research•2013

    The QPS is a novel instrument for the assessment of spasticity-related pain in children/adolescents with CP that was developed with direct patient input. Its modules allow the use of this instrument in children/adolescents with varied levels of impairment and communication skills

  • Equivalence and measurement properties of an electronic version of the Psoriasis Symptom Inventory

    Open Access•Donald M Bushnell, Mona L Martin et al.•ARTICLE•Quality of Life Research•2013

  • Content validity of the ASQoL for use in a non-radiographic axial spondyloarthritis population

    Open Access•Mark C Hwang, Mona L Martin et al.•ARTICLE•Quality of Life Research•2020

    Our results represent an important first step in confirming the relevance of the concepts in the ASQoL to patients with nr-axSpA, supporting quantitative assessment of ASQoL validity in this population

  • How patients being treated for non-small cell lung cancer value treatment benefit despite side effects

    Open Access•Mona L Martin, Julia R Correll et al.•ARTICLE•Quality of Life Research•2021

    In these two qualitative sub-studies, patients with advanced NSCLC valued the benefits of their treatment regardless of side effects that they experienced. Patients weighed their options against the seriousness of their disease and expressed their willingness to tolerate their side effects in return for receiving continued treatment benefits

  • Willingness to report treatment-related symptoms of immunotherapy among patients with non-small cell lung cancer

    Open Access•Mona L Martin, Helena Chung et al.•ARTICLE•Quality of Life Research•2021

    Patients have a range of reasons for not reporting their treatment-related symptoms when undergoing immunotherapy for NSCLC. Reasons are more strongly related to determination of the severity versus manageability of patients' experiences of symptoms than they are to the fear of having treatment discontinued

Medicine (10 works) · Physical therapy (6 works) · Psychology (5 works) · Internal Medicine (4 works) · Population (4 works) · Quality of life (healthcare (4 works) · Cognition (3 works) · Health Systems, Economic Evaluations, Quality of Life (3 works) · Nursing (3 works) · Psychometrics (3 works)

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