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Investigating the effectiveness of Mindfulness Based Stress Reduction(MBSR) through artificial intelligence on anxiety and pain caused by primary dysmenorrhea

Investigating the effectiveness of Mindfulness Based Stress Reduction(MBSR) through artificial intelligence on anxiety and pain caused by primary dysmenorrhea in the students of Medical Sciences

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250909067200N1
Enrollment
132
Registered
2025-09-21
Start date
2025-10-11
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Primary Dysmenorrhea. Pain and other conditions associated with female genital organs and menstrual cycle

Interventions

Intervention 1: Intervention group: Mindfulness-based stress reduction counseling through artificial intelligence. Intervention 2: Control group: During the study, people in the control group do not u

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Not having a known physical or mental illness or using anti-stress medications Absence of anxiety and depression No known chronic pelvic disease No surgery within the past three months Avoid using birth control pills, painkillers, and other herbal medicines, as well as relaxation or acupressure to relieve primary dysmenorrhea. Dysmenorrhea onset before age 20 and regular menstrual cycles with intervals of 21-35 days Mild to moderate pain intensity with a score of 4 to 8

Exclusion criteria

Exclusion criteria: Unwillingness to cooperate Having a known physical or mental illness or using anti-stress medications Having severe pain, scoring higher than 8 Dysmenorrhea starting after age 20 or having irregular menstrual cycles Using birth control pills, painkillers, and other herbal remedies, as well as relaxation techniques or acupressure to relieve primary dysmenorrhea History of surgery in the past three months Having a known chronic pelvic disease Suffering from anxiety and depression

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: Before and two weeks after the start of the intervention. Method of measurement: Spielberger State-Trait Anxiety Inventory.;Pain. Timepoint: Before and two weeks after the start of the intervention. Method of measurement: Pain intensity questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Behnam

Kerman University of Medical Sciences

bhnamfatmh468@gmail.com+98 935 926 6275

Outcome results

None listed

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