Polycystic Ovary Syndrome. Polycystic ovarian syndrome
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Ability to communicate and respond to the Multidimensional Fatigue Inventory and Visual Analogue Scale Age between 18 and 40 years Willingness to participate in the study and signing the informed consent form Definitive diagnosis of polycystic ovary syndrome by the relevant specialist physician Scoring 60 or above on the Multidimensional Fatigue Inventory Having chronic pain or similar symptoms such as lower abdominal pain or pain caused by ovarian issues No prior training or participation in studies similar to the current research within the past 6 months
Exclusion criteria
Exclusion criteria: Not meeting the inclusion criteria Presence of severe psychological disorders (such as major depression or severe anxiety) requiring specialized treatment Physical or mental disabilities—individuals who, due to their condition, are unable to perform relaxation or mindfulness exercises Use of sleeping pills, anti-anxiety, or antidepressant medications prior to the intervention Worsening of symptoms and the need for immediate medical treatment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The fatigue score is derived from the Multidimensional Fatigue Inventory. Timepoint: Before and after the interventions. Method of measurement: Multidimensional Fatigue Inventory.;Pain score based on Visual Analogue Scale. Timepoint: Severity of pain before, during and after the intervention. Method of measurement: Visual Analogue Scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Ahvaz University of Medical Sciences