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Background <p>Across low- and middle-income countries (LMICs), patients and the public remain involved only to a limited extent in respiratory health research. In this Photovoice project, people living with chronic respiratory diseases (CRDs) and carers partnered with the research team, shifting researcher-led processes towards co-production that influenced study design, conduct, analysis, and dissemination. This case study reports and reflects on the patient and public involvement (PPI) approach and its impacts.</p> Methods and processes <p>We conducted PPI-related activities throughout a Photovoice project to capture lived experiences of breathlessness, adaptation, and resilience across three engagement levels: (1) community awareness and screening, (2) healthcare-providers (HCPs) reflection, and (3) policy co-design. Two PPI carers reviewed all patient-facing materials for clarity and cultural sensitivity and advised on recruitment through treating physicians to build trust. Three PPI members and two participants contributed to the thematic validation. Participants took part in dissemination, co-curated the exhibitions and the <i>Living with CRD</i> photobook, and co-drafted a policy brief. The team thematically analysed reflections, discussions, and facilitator notes to identify key enablers and challenges.</p> PPI impact and reflections <p>PPI shaped every stage of the study. Their inputs influenced recruitment approaches, interpretation of lived-experience data, and design of dissemination materials. Participants described a sense of being ‘heard’ for the first time and expressed pride in contributing to change. The Photovoice exhibitions connected communities, clinicians, and policymakers, leading to co-developed recommendations through exhibition dialogues and the policy workshop.</p> Conclusion <p>This Photovoice project demonstrates how PPI partners can strengthen study relevance, enrich interpretation, and support dissemination to clinicians and policymakers in LMIC settings. Their engagement with design, analysis, and dissemination illustrates feasible co-production that builds trust, fosters empowerment and generates actionable, context-sensitive recommendations.</p>

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Amplifying the voices of people with chronic respiratory diseases (CRDs) care through photovoice: a case study of patient and public involvement in Klang, Malaysia

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年3月7日

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  • Jayakayatri Jeevajothi Nathan,
  • Hani Salim,
  • Ai Theng Cheong,
  • Norita Hussein,
  • Nik Sherina Hanafi,
  • Bee Kiau Ho,
  • Salbiah Mohamad Isa,
  • Noriah Ismail,
  • Fatin-Syazwani Abd-Malek,
  • Kent Ka Kian Goh,
  • Sheron Sir Loon Goh,
  • Nursyuhada Sukri,
  • Melissa Ali,
  • Mohammad Nur Eman Nazlan,
  • Tengku Azelawati Tuan Abdul Azid,
  • Hilary Pinnock,
  • Ee Ming Khoo

摘要

Background

Across low- and middle-income countries (LMICs), patients and the public remain involved only to a limited extent in respiratory health research. In this Photovoice project, people living with chronic respiratory diseases (CRDs) and carers partnered with the research team, shifting researcher-led processes towards co-production that influenced study design, conduct, analysis, and dissemination. This case study reports and reflects on the patient and public involvement (PPI) approach and its impacts.

Methods and processes

We conducted PPI-related activities throughout a Photovoice project to capture lived experiences of breathlessness, adaptation, and resilience across three engagement levels: (1) community awareness and screening, (2) healthcare-providers (HCPs) reflection, and (3) policy co-design. Two PPI carers reviewed all patient-facing materials for clarity and cultural sensitivity and advised on recruitment through treating physicians to build trust. Three PPI members and two participants contributed to the thematic validation. Participants took part in dissemination, co-curated the exhibitions and the Living with CRD photobook, and co-drafted a policy brief. The team thematically analysed reflections, discussions, and facilitator notes to identify key enablers and challenges.

PPI impact and reflections

PPI shaped every stage of the study. Their inputs influenced recruitment approaches, interpretation of lived-experience data, and design of dissemination materials. Participants described a sense of being ‘heard’ for the first time and expressed pride in contributing to change. The Photovoice exhibitions connected communities, clinicians, and policymakers, leading to co-developed recommendations through exhibition dialogues and the policy workshop.

Conclusion

This Photovoice project demonstrates how PPI partners can strengthen study relevance, enrich interpretation, and support dissemination to clinicians and policymakers in LMIC settings. Their engagement with design, analysis, and dissemination illustrates feasible co-production that builds trust, fosters empowerment and generates actionable, context-sensitive recommendations.