Literature DB >> 16220630

Respondent burden in clinical research: when are we asking too much of subjects?

Connie M Ulrich1, Gwenyth R Wallen, Autumn Feister, Christine Grady.   

Abstract

Keywords:  Biomedical and Behavioral Research

Mesh：

Year:  2005        PMID： 16220630

Source DB:  PubMed          Journal:  IRB        ISSN： 0193-7758


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  29 in total

1.  Evaluating quality of life in patients with asthma and rhinitis: English adaptation of the rhinasthma questionnaire.

Authors:  Hubert Chen; Miriam G Cisternas; Patricia P Katz; Theodore A Omachi; Laura Trupin; Edward H Yelin; John R Balmes; Paul D Blanc
Journal:  Ann Allergy Asthma Immunol       Date:  2011-01-08       Impact factor: 6.347

Review 2.  Emerging empirical evidence on the ethics of schizophrenia research.

Authors:  Laura B Dunn; Philip J Candilis; Laura Weiss Roberts
Journal:  Schizophr Bull       Date:  2005-10-19       Impact factor: 9.306

3.  Invited Commentary: The Tao of Clinical Cohort Analysis-When the Transitions That Can Be Spoken of Are Not the True Transitions.

Authors:  Stephen J Mooney
Journal:  Am J Epidemiol       Date:  2017-04-15       Impact factor: 4.897

4.  [As valuable as an organ donation. Enrollment in a clinical study requires patient willingness to make sacrifices].

Authors:  W Golder
Journal:  Z Rheumatol       Date:  2015-06       Impact factor: 1.372

5.  Development of the Lesbian, Gay, and Bisexual Affirmative Counseling Self-Efficacy Inventory - Short Form (LGB-CSI-SF).

Authors:  Frank R Dillon; Edward J Alessi; Shelley Craig; Ryan C Eber-Sole; Snehal M Kumar; Christine Spadola
Journal:  Psychol Sex Orientat Gend Divers       Date:  2015-03

6.  Perceptions of Response Burden Associated with Completion of Patient-Reported Outcome Assessments in Oncology.

Authors:  Thomas M Atkinson; Carolyn E Schwartz; Leah Goldstein; Iliana Garcia; Daniel F Storfer; Yuelin Li; Jie Zhang; Bernard H Bochner; Bruce D Rapkin
Journal:  Value Health       Date:  2018-08-31       Impact factor: 5.725

7.  Measurement properties of the Client-centered Care Questionnaire (CCCQ): factor structure, reliability and validity of a questionnaire to assess self-reported client-centeredness of home care services in a population of frail, older people.

Authors:  M E Muntinga; L B Mokkink; D L Knol; G Nijpels; A P D Jansen
Journal:  Qual Life Res       Date:  2014-02-28       Impact factor: 4.147

8.  Reducing patient burden to the FACT-Melanoma quality-of-life questionnaire.

Authors:  Richard J Swartz; George P Baum; Robert L Askew; Judy Lynn Palmer; Merrick I Ross; Janice N Cormier
Journal:  Melanoma Res       Date:  2012-04       Impact factor: 3.599

9.  Systematic review of global functioning and quality of life in people with psychotic disorders.

Authors:  A G Nevarez-Flores; K Sanderson; M Breslin; V J Carr; V A Morgan; A L Neil
Journal:  Epidemiol Psychiatr Sci       Date:  2018-10-01       Impact factor: 6.892

10.  Developing a Model of the Benefits and Burdens of Research Participation in Cancer Clinical Trials.

Authors:  Connie M Ulrich; Kathleen A Knafl; Sarah J Ratcliffe; Therese S Richmond; Christine Grady; Claiborne Miller-Davis; Gwenyth R Wallen
Journal:  AJOB Prim Res       Date:  2012
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