Condition 1: Cyclic mastalgia. Condition 2: sexual satisfaction. Condition 3: sexual distress. Mastodynia
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Having breast pain for more than 5 days per month according to the Cardiff breast pain table and pain intensity greater than 4 in every 5 days according to the objective pain ruler . Married women Age range of 20 years to before menopause Having regular menstrual periods Willingness to participate in the study
Exclusion criteria
Exclusion criteria: Having marital conflicts based on the person's statement Pregnancy Breastfeeding Suffering from physical and mental illnesses (self-reported) Personal or family history of breast cancer receiving medical treatment to reduce breast pain in the last three months Using hormonal methods to prevent pregnancy History of surgery or breast sampling
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sexual satisfaction score in the Sexual Satisfaction Scale for Women. Timepoint: Measurement of sexual satisfaction at the beginning of the study (before the intervention) and in the follow-ups one and three months after the intervention. Method of measurement: The Sexual Satisfaction Scale for Women.;Sexual distress score in the Sexual Satisfaction Scale for Women. Timepoint: Measurement of sexual distress at the beginning of the study (before the intervention) and in the follow-ups one and three months after the intervention. Method of measurement: The Sexual Satisfaction Scale for Women.;Mindfulness score in The Five Facet Mindfulness Questionnaire. Timepoint: Measurement of mindfulness at the beginning of the study (before the intervention) and in the follow-ups one and three months after the intervention. Method of measurement: The Five Facet Mindfulness Questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| The intensity of breast pain according to the score of Visual analog scale. Timepoint: At the beginning of the study (before the start of the intervention) and in the follow-ups 1 and 3 months after the intervention. Method of measurement: Visual analog scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Qazvin University of Medical Sciences