Comparative investigation between the effectiveness of Dry Cupping and counselling with Mindfulness-Based Cognitive Therapy approach (MBCT) on women’s conception rate with Poly-Cystic Ovary Syndrome

INTERVENTION: Intervention 1: In Intervention group, dry cupping therapy is performed by three special glasses twice a week for two months during the cleansing period .The dry cupping will put under the abdomen in the upper pubic area . The glasses or cups for cupping have 5 sizes that are selected according to the size of the individual. The person is placed on the bed lying on his back and where the cupping is performed is exposed. The first cup is placed above the pubis symphysis or four fingers below the umbilicus. The other two glasses are placed to the right and left of the first glass at a distance of about 2.5 cm, and again their distance to the umbilicus of four fingers is closed. The end of the cups is connected to the suction device. The body is sucked towards the top of the glass and becomes red and full of blood. The glasses remain for seven minutes and then the suction is cut off and the cups are gently removed . In fact, 12 sessions of cupping therapy should be performed in two months. All members of this group were referred to Hakim Emadeddin Shirazi Health Center of Iranian Medicine in Shiraz for cupping and were performed by a trained minister under the supervision of a traditional medicine specialist. Intervention 2: Intervention group: Counseling group with Mindfulness‐Based Cognitive Therapy approach (MBCT):In this group, eight sessions will be held for 120 to 150 minutes with 45 minutes a day of exercise, which can be accompanied by a one‐day mind‐guided program in 6th week. In the first 4 sessions, the focus is on inner experiences and in the second half is on life challenges. All sessions begin with a formal exercise (body checking, mindfulness movement, or sitting meditation practice).Short mindfulness exercises, such as three‐minute breathing and conscious w CONDITION: infertile women due to poly cystic ovary syndrome. PRIMARY OUTCOME: Conception rate. Timepoint: Fertilization rate will assess based on Beta HCG test in all three groups(if delayed menstruation occurs) at four times: immediately after treatment, one month after treatment, two months after treatment, three months after treatment. Method of measurement: Beta HCG test. SECONDARY OUTCOME: Changes in Luteinizing hormone. Timepoint: At four times: immediately after the end of treatment, one month after the end of treatment, two months after the end of treatment, three months after the end of treatment. Method of measurement: Luteinizing hormone test. INCLUSION CRITERIA: Married women with infertility with definitive diagnosis of polycystic ovary syndrome based on Rotterdam criteria by gynecologists Lack of known mental illnesses under treatment Do not use psychotropic drugs and narcotics Married women Ability to read, write and speak Persian Do not attend counseling sessions or medication for fertility Couples agree to have vaginal sex (for example, two to three times a week) around the time of ovulation during the time of the study No endometrial cancer or cervical cancer The subject should not have a history of deep vein thrombosis or pulmonary embolism