Vaginismus. Vaginismus
Conditions
Interventions
Intervention 1: The first intervention group: providing transcranial electrical stimulation of the brain using direct current (tDCS) in the form of ten 20-minute sessions with an intensity of two mill
Sponsors
University of Lorestan
Eligibility
Sex/Gender
Female
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: All women diagnosed with vaginismus disorder who have at least a diploma. All women diagnosed with vaginismus disorder who do not have psychotic symptoms. All women diagnosed with vaginismus disorder who do not have substance abuse and psychological disorders (as diagnosed by a psychiatrist or psychologist). All women diagnosed with vaginismus disorder who do not have gynecological diseases (such as infection). All women diagnosed with vaginismus disorder who have been married for at least 1 to 3 years.
Exclusion criteria
Exclusion criteria: All women who have any disorder except vaginismus disorder. All women who have symptoms similar to vaginismus but do not have a Gynecologist diagnosis. All women who are not married or have been married for less than a year. All women who are under 18 years old and over 50 years old. All women who have symptoms of psychosis and take nerve medication. All women whose educational qualification is below diploma.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcome: sexual pain score. Timepoint: 1 to 5 days before the intervention and 1 to 5 days after the intervention. Method of measurement: McGill pain questionnaire.;Secondary outcome: anxiety score. Timepoint: 1 to 5 days before the intervention and 1 to 5 days after the intervention. Method of measurement: Kettle Anxiety Questionnaire.;Individual's executive performance scores. Timepoint: 1 to 5 days before the intervention and 1 to 5 days after the intervention. Method of measurement: Nback memory test, Wisconsin test, Semantic Stroop test. | — |
Secondary
| Measure | Time frame |
|---|---|
| Sexual pain score. Timepoint: Before intervention and after intervention. Method of measurement: McGill Sexual Pain Questionnaire 22 questions.;Anxiety. Timepoint: Before intervention and after intervention. Method of measurement: Kettle Anxiety Questionnaire 40 questions.;Executive functions. Timepoint: Before intervention and after intervention. Method of measurement: Semantic Strope, NB Memory Test, Wisconsin Test. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contactmotahareh nosratabadi
the university of lorestan
Outcome results
None listed