Investigating the effect of mindfulness based cognitive therapy on sexual satisfaction and distress of married women with cyclic mastalgia

Not Applicable

Conditions: Condition 1: Cyclic mastalgia. Condition 2: sexual satisfaction. Condition 3: sexual distress.
Mastodynia
N64.4

Registration Number: IRCT20240520061847N1

Lead Sponsor: Qazvin University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Pending

Sex: Female

Target Recruitment: 72

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

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

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
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.