# The importance of partnership in chronic pain – co-creation of tomorrow's pain care by working together in research, implementation, and knowledge dissemination

**Authors:** Paulin Andréll, Birgit Heckemann, Anna Grimby-Ekman, Gunilla Göran, Marie-Louise Olsson, Roger Johansson, Paula Forslund, Axel Wolf

PMC · DOI: 10.3389/fpain.2026.1765233 · Frontiers in Pain Research · 2026-03-09

## TL;DR

This paper emphasizes the value of collaboration between patients, healthcare professionals, and researchers to improve chronic pain care and raise awareness.

## Contribution

The paper highlights the role of partnership and patient involvement in co-creating effective chronic pain care strategies.

## Key findings

- Partnership between patients and healthcare professionals improves clinical and economic outcomes in pain care.
- Patient and public involvement helps identify deficiencies in pain care and shape relevant research.
- Collaboration leads to better awareness and implementation of chronic pain research in clinical practice.

## Abstract

Chronic pain is a long-term condition that affects the daily lives, identities, and well-being of millions of people worldwide. Effective pain care remains limited. Moreover, lack of knowledge and awareness among healthcare professionals and patients, combined with the invisibility of pain, often leads to disbelief, delayed diagnosis, prolonged suffering, and significant societal costs. Novel approaches are necessary to improve pain care, as most countries’ healthcare systems are struggling to provide adequate support for persons living with chronic pain. This article highlights the importance of partnership in chronic pain management. We present examples from Sweden that demonstrate the benefits of stakeholder collaboration to improve pain care. Partnership between patients and healthcare professionals is a core element of person-centered care (PCC). We present PCC as a necessary strategy that combines ethical commitment with demonstrable clinical and economic benefits. We highlight the unique value of patient and public involvement (PPI) in pain research and innovation, where patients with lived experience can help researchers identify deficiencies in pain care and service provision, formulate relevant research questions, and develop projects that address real needs and priorities. Finally, we provide concrete examples of successful cooperation between patients, healthcare professionals, patient associations, and researchers in raising awareness of chronic pain and translating research findings into clinical practice. Collaboration among healthcare professionals, patient associations, and researchers is essential to make the best use of knowledge and lived experience to co-create and implement effective pain care, advance research, and raise awareness of chronic pain in healthcare and society.

## Full-text entities

- **Diseases:** pain (MESH:D010146), Chronic pain (MESH:D059350)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC13006614/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC13006614/full.md

---
Source: https://tomesphere.com/paper/PMC13006614