Skip to content

A Comparative Study of the Impact of Progressive Muscle Relaxation and Mindfulness Artificial Intelligence-Based on Fatigue Levels and Pain Intensity

A Comparative Study of the Impact of Progressive Muscle Relaxation and Mindfulness Artificial Intelligence-Based on Fatigue Levels and Pain Intensity in Women Suffering from Polycystic Ovary Syndrome: A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200107046044N5
Enrollment
72
Registered
2025-06-09
Start date
2025-07-23
Completion date
Unknown
Last updated
2025-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Polycystic Ovary Syndrome. Polycystic ovarian syndrome

Interventions

Intervention 1: Intervention Group 1: Progressive Muscle Relaxation (PMR): In this group, the patient is placed in a lying down and comfortable position. On the first day, the relaxation training incl

Sponsors

Yasouj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

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

MeasureTime 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

Public ContactMohammadSajjad Mousavi

Ahvaz University of Medical Sciences

sajjad.mousavi2512@gmail.com+98 61 5242 1065

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026