Primary dysmenorrhea.
Conditions
Interventions
Intervention 1: Intervention group: Hypnotherapy. Hypnotherapy will be performed in three sessions of 20 minutes for the experimental group individually.In the first session, hypnotherapy is introduce
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Conscious consent to participate in research Single students living in dormitories Suffering age 25-18 years Having regular menstrual periods Having primary dysmenorrhea for at least two consecutive previous periods No application of complementary medicine methods during the last two months Painful menstruation in most menstrual cycles with a pain score of at least 4 out of 10 according to the Visual Analogue Scale (VAS) during two periodic periods Hypnosis of people
Exclusion criteria
Exclusion criteria: Any known disease of the genital tract Secondary dysmenorrhea History of abdominal or pelvic surgery Endometriosis Tobacco use (cigarettes, hookah and drugs), alcohol Speech, hearing, and mental problems Heart, kidney, respiratory, diabetes, asthma, hypothyroidism or hyperthyroidism, epilepsy and other patients in need of medication Sudden weight loss Special diet (vegetarian) Do professional exercise and intense physical exercises Use of herbs, traditional and complementary medicine during the last two months Psychological problems and diseases requiring medication (bipolar disorder, psychosis, major depression, obsession, borderline disorders, dependent personality disorder, schizoid personality disorder, paranoid personality disorder) based on self-reported research units Having coagulation disorders and taking anticoagulants Existence of depression in the individual based on the score obtained from the DASS21 questionnaire
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain score. Timepoint: Before. Immediately and two months after the intervention. Method of measurement: Pain ruler.;Number of pain days. Timepoint: Before. Immediately and two months after the intervention. Method of measurement: Asking the patient.;Bleeding volume. Timepoint: Before. Immediately and two months after the intervention. Method of measurement: PBLAC chart. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Mahboobeh Valiani
Esfahan University of Medical Sciences
Outcome results
None listed