The comparison of in person pelvic floor physiotherapy for vaginismus with not in person online treatment
Not Applicable
- Conditions
- vaginismus.VaginismusN94.2
- Registration Number
- IRCT20140811018760N8
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 70
Inclusion Criteria
The study subjects are women suffering from vaginismus who will refer to the mentioned centers in 2023-2024. Based on DSM-5 criteria, the participants will enter the intervention group (in-person treatment) and the control group (not in-person treatment). Participants will be 20-40 years with severity of vaginismus 3 or 4 according to the Lamont classification (5-8).
Exclusion Criteria
Secondary vaginismus, lack of cooperation to continue treatment and follow-up evaluation, untreated vaginal infection, perineal ulcer, anal ulcer, neuromuscular diseases such as myasthenia gravis, vulvodynia, urinary tract problems.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Successful and painless penetration report. Timepoint: At the beginning(before the start of intervention) and 14 days and 6 months after the start of the intervention. Method of measurement: patient report.
- Secondary Outcome Measures
Name Time Method Vaginismus severity. Timepoint: at the beginning (before the start of intervention) and 14 days and 6 months after beginning of the intervention. Method of measurement: Lamont scale.;Pain intensity. Timepoint: at the beginning (before the start of intervention) and 14 days and 6 months after beginning of the intervention. Method of measurement: numerical pain score (NPS).;Sexual function. Timepoint: at the beginning (before the start of intervention) and 14 days and 6 months after beginning of the intervention. Method of measurement: female sexual function index.