Grant: Project Grant
Université de Sherbrooke
$730,576.00
Efficacy of dry needling for reducing pain during intercourse in women with provoked vestibulodynia: A multicenter randomized controlled trial
FY 2024-25
Summary
Chronic vulvar pain is a highly prevalent and debilitating condition affecting up to 16% of women. The most common subtype of vulvar pain, provoked vestibulodynia (PVD), is characterized by a sharp pain at the entry of the vagina in response to pressure or attempted vaginal penetration. Women with PVD not only present with psychological distress and significant disruption in all aspects of sexual function, but they are also confronted with limited effective treatment options. Dry needling (DN) could fill this therapeutic gap. Similar to acupuncture, this approach involves the insertion of fine needles into the tissues. However, its mechanisms of action are quite different. DN specifically targets muscle tension/stiffness, which has been shown to play a key role in PVD. Therefore, our multidisciplinary team, working together for more than 15 years, has conducted novel research to prepare for the current proposal. We have developed cutting-edge technologies to assess the pelvic floor muscles (PFM), acquired internationally recognized expertise in DN, and studied its effects on skeletal muscles and pain control mechanisms. After designing a DN treatment protocol tailored to the affected muscles in PVD, our randomized pilot study confirmed that our state-of-the-art DN treatment protocol is feasible and acceptable for treating PVD and the promising findings obtained provide support for conducting a large-scale study.
The proposed multicenter double-blind randomized controlled trial aims to establish the efficacy of DN for reducing pain in women with PVD. Women will be randomized to receive either sham or real DN for 8 weekly sessions. Validated outcome measures will be assessed at baseline, post-treatment and at the 6-month follow-up.
The current proposal addresses the urgent need to develop novel treatment options for women with PVD. If proven effective, DN could be proposed as a first-line low-risk treatment.
Department
Program
Project Grant
Recipient
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
523751
Name
Morin Melanie
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Gender and Health
Theme2
Clinical
Prcname2
Gender, Sex & Health
Projecttitle
Efficacy of dry needling for reducing pain during intercourse in women with provoked vestibulodynia: A multicenter randomized controlled trial
Programtype2
Operating Grants
Orgnameinp2
Université de Sherbrooke
Cihramount2
$730,576
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Chronic Pelvic Pain; Dry Needling; Dyspareunia; Elastography; Pelvic Floor Dysfunction; Physiotherapy; Sexual Function; Vulvodynia; Women'S Health
Abstract
Chronic vulvar pain is a highly prevalent and debilitating condition affecting up to 16% of women. The most common subtype of vulvar pain, provoked vestibulodynia (PVD), is characterized by a sharp pain at the entry of the vagina in response to pressure or attempted vaginal penetration. Women with PVD not only present with psychological distress and significant disruption in all aspects of sexual function, but they are also confronted with limited effective treatment options. Dry needling (DN) could fill this therapeutic gap. Similar to acupuncture, this approach involves the insertion of fine needles into the tissues. However, its mechanisms of action are quite different. DN specifically targets muscle tension/stiffness, which has been shown to play a key role in PVD. Therefore, our multidisciplinary team, working together for more than 15 years, has conducted novel research to prepare for the current proposal. We have developed cutting-edge technologies to assess the pelvic floor muscles (PFM), acquired internationally recognized expertise in DN, and studied its effects on skeletal muscles and pain control mechanisms. After designing a DN treatment protocol tailored to the affected muscles in PVD, our randomized pilot study confirmed that our state-of-the-art DN treatment protocol is feasible and acceptable for treating PVD and the promising findings obtained provide support for conducting a large-scale study.
The proposed multicenter double-blind randomized controlled trial aims to establish the efficacy of DN for reducing pain in women with PVD. Women will be randomized to receive either sham or real DN for 8 weekly sessions. Validated outcome measures will be assessed at baseline, post-treatment and at the 6-month follow-up.
The current proposal addresses the urgent need to develop novel treatment options for women with PVD. If proven effective, DN could be proposed as a first-line low-risk treatment.
Competitiondate
202503
Approvedterm2
4 yrs 0 mth
Pinamesdelim
Morin, Melanie
Approvedterm
4 ans 0 mois
Cihrcontribution2
~ $730,576~ $0~