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Published on: February 16, 2011
Co-Designing a Quality of Life Survey for Mesothelioma: Qualitative and Cognitive Interview Findings
Clare O'Callaghan1, Joanne Brooker2, Sanuki Tissera3
1Caritas Christi and Department of Psychosocial Cancer Care (C.O.C.), St Vincent's Hospital Melbourne, Melbourne, Victoria, Australia; Department of Medicine (C.O.C.), St Vincent's Hospital, The University of Melbourne, Melbourne, Victoria, Australia.
Context:
Mesothelioma is a rare, incurable, and aggressive cancer and "patient-reported outcome" (PRO) data from people living with mesothelioma (PLM) are lacking.
Objectives:
To examine PLM's views about, and cognitive processes whilst answering, a draft quality of life and care survey, to inform survey refinements and implementation into the Victorian Mesothelioma Outcome Registry (VMOR), Australia.
Methods:
Constructivist (qualitative) and co-designed study. An expert-developed draft PRO survey comprised the: EORTC QLQ-C30 health-related quality of life question-set, Australian Hospital Patient Experience Question Set (AHPEQS), and demographic / mesothelioma background questions. Telephone semi-structured and "think aloud" interviews examined PLM's survey views and cognitive processes during responses. Concurrent inductive thematic analysis (survey views) and deductive content analysis (cognitive processes) proceeded.
Results:
PLM believed that the survey would produce information important for improving PLM healthcare but made many content and layout suggestions to reduce respondent confusion, inappropriate answers, and burden. Free-text response options were strongly recommended. Survey content was generally nondistressing but could elicit challenging memories and need for support. Several PLM displayed challenges in executing cognitive processes during survey responses, notably on whether EORTC-QL30 referred to general or mesothelioma-only related health and which hospital care experience the AHPEQS referred to.
Conclusion:
A refined co-designed VMOR PRO survey should yield patient-meaningful qualitative and quantitative evidence to guide the Registry's leadership in what issues are important to patients and their clinical team. While co-designed "viewpoint seeking" and cognitive interviewing studies can improve valid survey outcomes, PRO responses may also be affected by extraneous circumstances, including comorbidities.
Insights
Patient-reported outcome (PRO) data from people with mesothelioma (PLM) is scarce. This study refined a PRO survey through PLM feedback, improving its relevance and usability for mesothelioma care.
Area of Science:
- Oncology
- Patient-Reported Outcomes
- Qualitative Research
Background:
- Mesothelioma is a rare, aggressive cancer with limited patient-reported outcome (PRO) data.
- Understanding the experiences of people living with mesothelioma (PLM) is crucial for improving care.
Purpose of the Study:
- To co-design and refine a PRO survey for the Victorian Mesothelioma Outcome Registry (VMOR).
- To gather PLM perspectives on a draft quality of life and care survey.
- To inform survey implementation by examining PLM's views and cognitive responses.
Main Methods:
- A qualitative, co-designed study using semi-structured and "think aloud" interviews.
- Incorporated the EORTC QLQ-C30, AHPEQS, and demographic/mesothelioma background questions.
- Employed thematic and content analysis to evaluate survey views and cognitive processes.
Main Results:
- PLM provided valuable feedback for survey refinement, suggesting content and layout improvements.
- Free-text response options were recommended to reduce confusion and burden.
- Some participants experienced cognitive challenges with specific survey questions, highlighting the need for clarity.
Conclusions:
- A refined, co-designed VMOR PRO survey will provide patient-meaningful data for healthcare improvement.
- Co-design and cognitive interviewing enhance survey validity.
- PRO data collection should consider potential impacts of comorbidities and other external factors.
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