Patients' Attitudes and Preferences About Participation and Recruitment Strategies in Clinical Trials
Authors:
- Amit SoodASAmit Sood
- Kavita PrasadKPKavita Prasad
- Laveena ChhatwaniLCLaveena Chhatwani
- Eri ShinozakiESEri Shinozaki
- Stephen S. ChaSCStephen S. Cha
- Laura L. LoehrerLLLaura L. Loehrer
- Dietlind L. Wahner-RoedlerDWDietlind L. Wahner-Roedler
- 1 March 2009
- journal article
- Published by Elsevier in Mayo Clinic Proceedings
- Vol. 84 (3) , 243-247
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- Offering participants results of a clinical trial: sharing results of a negative studyThe Lancet, 2005
- Public Attitudes Regarding Willingness to Participate in Medical Research StudiesSocial Work in Public Health, 2000
- Relation between agendas of the research community and the research consumerThe Lancet, 2000
- Barriers to Participation in Randomised Controlled TrialsJournal of Clinical Epidemiology, 1999
- Ethical aspects of clinical trials: the attitudes of the public and out‐patientsJournal of Internal Medicine, 1999
- What do I want from health research and researchers when I am a patient?BMJ, 1995
- The Recruitment of Research Participants:Social Work in Health Care, 1993
- Recruitment experience in clinical trials: Literature summary and annotated bibliographyControlled Clinical Trials, 1987
- Applying results of randomised trials to clinical practice: impact of losses before randomisation.BMJ, 1984
- Streptomycin Treatment of Pulmonary Tuberculosis: A Medical Research Council InvestigationBMJ, 1948