Patients’ priorities concerning health research: the case of asthma and COPD research in the Netherlands
Open Access
- 2 August 2005
- journal article
- Published by Wiley in Health Expectations
- Vol. 8 (3) , 253-263
- https://doi.org/10.1111/j.1369-7625.2005.00337.x
Abstract
Background Although patients are increasingly involved in agenda setting within specific fields of health research, they rarely participate in decision-making on the entire breadth of health research, including biomedical research. This might be attributable to a widely held view that patients are incapable of adequate research prioritization due to a lack of relevant knowledge, a failure to look beyond their own individual problems or an inability to objectively consider long-term targets. Aims By conducting transparent and structured consultations with asthma and chronic obstructive pulmonary disease (COPD) patients regarding their health research priorities, we aim to assess the ability of patients to prioritize research in a well-argued way. Methods Patients were consulted through seven focus groups, a feedback meeting, and a questionnaire. The focus groups and the feedback meeting aimed to explore the entire breadth of patients’ problems experienced in relation to their diseases, while the questionnaire aimed to investigate patients’ prioritization of possible research targets focused on solving these problems. Results The focus groups produced a wide range of problems, including those related to health-care organization, social environment, therapy and costs. In terms of research prioritization, patients focused primarily on biomedical issues, particularly aetiology, co-morbidity and effective medication. Conclusions The consultation procedure successfully elicited patients’ research priorities including the underlying arguments. Our results indicate that asthma and COPD patients are capable of research prioritization in a well-argued way and that they highly value biomedical research. Furthermore, as they prioritized some research topics that are not covered by current Dutch research programmes, we argue that patient participation can broaden research agenda setting.Keywords
This publication has 14 references indexed in Scilit:
- Involving consumers in research and development agenda setting for the NHS: developing an evidence-based approachHealth Technology Assessment, 2004
- Development of the National Eye Institute refractive error correction quality of life questionnaire: Focus groupsOphthalmology, 2003
- Involving users in low back pain researchHealth Expectations, 2003
- Overcoming the challenges to consumer involvement in cancer researchHealth Expectations, 2003
- Consumer involvement in health research: fact or fiction?British Journal of Clinical Governance, 2002
- Institutionalizing a transdisciplinary approach to technology development in a Bangladeshi NGOInterdisciplinary Environmental Review, 2002
- The development and validation of a dysphagia-specific quality-of-life questionnaire for patients with head and neck cancer: the M. D. Anderson dysphagia inventory.2001
- Public involvement in health care priority setting: an overview of methods for eliciting valuesHealth Expectations, 1999
- Focus GroupsAnnual Review of Sociology, 1996
- Public health research and lay knowledgeSocial Science & Medicine, 1996