CompletedNot Applicable

Somatocognitive Therapy in Treatment of Provoked Vestibulodynia - a Feasibility Study

Norway10 participantsStarted 2019-02-01

Plain-language 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.

Who can participate

Age range18 Years – 35 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Confirmed provoked vestibulodynia diagnosis Exclusion Criteria: * vulvar pain is not clearly linked to intercourse or pressure applied to vestibule or usage of tampon * active infection or dermatologic lesion in the vulvar region

What they're measuring

Recruitment rate

Timeframe: 5 months

Follow-up rate

Timeframe: 8 months

Adherence

Timeframe: 8 months

Evaluation of Tampon test as a primary outcome measure - score variance

Timeframe: 8 months

Adverse events

Timeframe: 8 months

Evaluation of Tampon test as a primary outcome measure - qualitative interviews

Timeframe: 8 months

Trial details

NCT IDNCT04208204

SponsorOslo Metropolitan University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2020-07-31

View on ClinicalTrials.gov More Provoked Vestibulodynia trials