Condition 1: Premenstrual syndrome. Condition 2: Premenstural Syndrome. Condition 3: Premenstural Syndrome. Condition 4: Premenstural Syndrome. Eating disorders Nonorganic sleep disorders Psychological and behavioural factors associated with disorders or diseases classified elsewhere Unspecified behavioural syndromes associated with physiological disturbances and physical factors
Conditions
Interventions
Intervention 1: The first group (intervention): Perform 8 Sessiones of Auriculotherapy once a week, stimulate pointes of both ears for 5 to 15 seconds by (Excel Pointer) at every meeting. After Auric
The first group (intervention): Perform 8 Sessiones of Auriculotherapy once a week, stimulate pointes of both ears for 5 to 15 seconds by (Excel Pointer) at every meeting. After Auriculotherapy in ea
The second group (intervention): Perform 8 sessions of Mindfulness based cognitive behavioral therapy once a week for 90-120 minutes.
Control group: Before intervention, Week Eight and The twelfth week after the intervention, Will be completed the screening tool premenstrual syndrome. this group will not receive any intervention. bu
Sponsors
Vice Chancellor for Research of Shahid Sadoughi University of Medical Science
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: female students living in dormitories University of Medical Sciences; Having two healthy ears (for auriculotherapy); no history or treatment of disorders like depression or anxiety; eating disorders; anemia; thyroid disease; diabetes; lack of birth control pills for medical reasons; Not taking any herbal medicine and effective treatment of premenstrual syndrome; Not treated with drugs; mental disorders and other non-pharmacological methods; Having at least 30% increase in severity of symptoms within 5 days before menstruation; Non-participation in another related study until the completion of the current study period. Exclusion criteria: Premenstrual dysphoric disorder.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Premenstrual syndrome. Timepoint: Before the intervention, after intervention and one month after intervention. Method of measurement: Premenstrual syndrome screening tool. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactBtoul ghaeidamini
shaheid sadoughi University of Medical Sciences
Outcome results
None listed