Ignite Creation Date:
2024-05-06 @ 7:08 PM
Last Modification Date:
2024-10-26 @ 3:01 PM
Study NCT ID:
NCT05909514
Status:
RECRUITING
Last Update Posted:
2024-01-09
First Post:
2023-05-05
Brief Title:
Investigating the Effectiveness of PelvicSenseR on Pain and Sexual Outcomes in Provoked Vestibulodynia
Sponsor:
Dr Caroline Pukall
Organization:
Queens University
Study Overview
Official Title:
Investigating the Effectiveness of PelvicSenseR on Pain and Sexual Outcomes in Provoked Vestibulodynia
Status:
RECRUITING
Status Verified Date:
2024-01
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study will examine the effectiveness of the PelvicSense 3-month online program on pain and other outcomes in those with provoked vestibulodynia This study is prospective in nature and will involve several assessment points baseline immediately post-treatment at the end of the 3 month program and 3-month follow up All aspects of the study will be conducted remotely eg online email video calls and participants will be at least 18 years of age fluent in English and experience pain due to provoked vestibulodynia for at least 3 months with a physician diagnosis Participants are expected to continue their treatment as usual and this information will be documented throughout the study
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None