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A randomized controlled trial investigating feasibility, acceptability and effects of dry needling for provoked vestibulodynia

J Pain. 2025 Nov 7:105596. doi: 10.1016/j.jpain.2025.105596. Online ahead of print.

ABSTRACT

This study aimed to investigate the feasibility, acceptability, and effects of dry needling in women with provoked vestibulodynia. Forty-six women diagnosed with provoked vestibulodynia were randomized to receive six weekly sessions of either real or sham dry needling. Participants, investigators and data analysts were blinded. Feasibility outcomes (adherence to treatment, questionnaire completion and dropout rate) and side effects were measured throughout the study. Pain intensity during intercourse (numeric rating scale) was measured at baseline and posttreatment, and acceptability (questionnaire) was assessed posttreatment. Women in the realDN group attended 99% of the planned treatment sessions, compared to 91% in the shamDN group. Additionally, 100% of questionnaires were completed in the realDN group, compared to 93% in the shamDN group. All participants in the realDN group completed the study. In contrast, two participants in the shamDN group withdrew. For the main side effects, 96% of the participants in the realDN group and 52% in the shamDN group experienced muscle aches (p <.001). Moreover, 35% experienced autonomic reactions in the realDN group, while these were not observed in the shamDN group (p <. 001). All participants reported high levels of acceptability across all dimensions, with no significant difference between groups. The realDN group showed a significant decrease in pain intensity compared to the shamDN group (mean difference between groups 2.4; 95%CI 1.4-3.3; p <.001). Our findings support the feasibility and acceptability of dry needling to treat women with provoked vestibulodynia and showed a significant effect in reducing pain. PERSPECTIVE: This article presents the results of a novel study examining the feasibility and acceptability of using dry needling to treat women suffering from provoked vestibulodynia and lays the groundwork to inform a future randomized controlled trial.

PMID:41207407 | DOI:10.1016/j.jpain.2025.105596

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