Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/37854
Appears in Collections:Psychology Journal Articles
Peer Review Status: Refereed
Title: Research priorities in vulvodynia: A modified Delphi study
Author(s): Lountzi, Athina Zoi
Abhyankar, Purva
Durand, Hannah
Contact Email: athinazoi.lountzi@stir.ac.uk
Keywords: vulvodynia
research
prioritisation
expert engagement
Issue Date: 2025
Date Deposited: 21-Oct-2025
Citation: Lountzi AZ, Abhyankar P & Durand H (2025) Research priorities in vulvodynia: A modified Delphi study. <i>Women's Health</i>, 21. https://doi.org/10.1177/17455057251378957
Abstract: Background: Vulvodynia is a chronic, unexplained pain in and around the vulva, likely involving an interplay of biological and psychosocial factors. Women with vulvodynia often experience delayed diagnoses, ineffective treatments, and significant quality of life impacts, compounded by social stigma and negative healthcare experiences. Despite its prevalence, our understanding of vulvodynia and its impacts remains limited. Objectives: To establish research priorities that address critical knowledge deficits and improve outcomes for individuals affected by vulvodynia. Design: A mixed-methods participatory study using a modified electronic Delphi (e-Delphi) approach combined with focus groups. Methods: A three-phase modified e-Delphi process was combined with focus groups to gather insights from patients, clinicians, and researchers with expertise in vulvodynia. In Phase 1, participants generated research topics through surveys and focus group discussions. In Phase 2, these topics were rated and ranked by participants to generate a preliminary “top 10” list of priorities. In Phase 3, participants re-rated and re-ranked the preliminary list to achieve consensus on the final research priorities. Results: The top three priorities identified were: (1) Creating a person-centred care pathway and increasing awareness, education, and training of clinicians on vulvodynia, (2) Development of multidisciplinary pain teams, and (3) Creating accessible information for patients on treatment options and self-care advice. Conclusion: This study highlights the importance of integrating the perspectives of those with lived experience, healthcare professionals, and researchers to identify research priorities with the greatest potential for impact. Findings provide a roadmap for future vulvodynia research, support efficient resource allocation, and inform policy development. Furthermore, these results provide a foundation for grassroots initiatives to improve awareness, education, and care for individuals affected by vulvodynia.
DOI Link: 10.1177/17455057251378957
Rights: This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
Licence URL(s): http://creativecommons.org/licenses/by/4.0/

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