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Somatocognitive Therapy in Treatment of Provoked Vestibulodynia - a Feasibility Study — ProLoVe  

Provoked Vestibulodynia Clinical Trial

Official title:
Somatocognitive Therapy in Treatment of Provoked Vestibulodynia - Process of Change and User Experience

Clinical Trial Summary

This study examines feasibility of R&D activities in the planned randomized controlled trial where effectiveness of somatocognitive therapy intervention will be compared to treatment as usual in provoked vestibulodynia.

Clinical Trial Description

Provoked vestibulodynia is a multifactorial, persistent pain condition, affecting young women. It represents the most common cause of pain during sexual intercourse. Existing treatment approaches are predominantly based on clinical experience, observational studies, or reports of expert committees. Although, physiotherapy is one of the most commonly recommended treatments, high quality randomized controlled trials are needed to assess its effectiveness.

This is a phase I, feasibility study with the purpose of testing R&D activities for a planned full size RCT. Additionally, patients experiences with the somatocognitive therapy intervention, assessment measures and condition itself will be collected using qualitative interviews. The results will be applied to adjust time-line of the treatment, outcome measures and therapeutic approach before commencing full scale RCT. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04208204
Study type Interventional
Source Oslo Metropolitan University
Contact
Status Completed
Phase N/A
Start date February 1, 2019
Completion date July 31, 2020
View Details
See also
  Status Clinical Trial Phase
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Recruiting NCT05909514 - Investigating the Effectiveness of PelvicSense(R) on Pain and Sexual Outcomes in Provoked Vestibulodynia N/A
Completed NCT04234542 - Is Low Level Laser Therapy (LLLT) Effective for Reducing Pain Experienced by Women With Provoked Vestibulodynia? N/A
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