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The effect of computer-based Stress Inoculation Training (SIT) approach on the pelvic pain, depression, and anxiety in students with primary dysmenorrhea

The effect of computer-based Stress Inoculation Training (SIT) approach on the pelvic pain, depression, and anxiety in students with primary dysmenorrhea

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230130057274N5
Enrollment
100
Registered
2024-04-29
Start date
2021-12-01
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Condition 1: Pelvic pains. Condition 2: Anxiety and depression. Diseases of the genitourinary system Mixed anxiety and depressive disorder

Interventions

Intervention group: Sit treatment method.

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 38 Years

Inclusion criteria

Inclusion criteria: Being Iranian Declaration of consent to participate in the study Age range from 18 to 38 years Having any degree (one, two, or three) of primary dysmenorrhoea having regular menstrual cycles with intervals of 21 to 35 days and a duration of 3 to 10 days at least during the last six months Obtaining a score of 8 or higher on the HADS questionnaire Access to smartphones

Exclusion criteria

Exclusion criteria: History of genital diseases, surgery, and known and chronic underlying diseases Taking birth control pills Having hormonal disorders, irregular menstruation Pelvic infection, burning and itching, and abnormal vaginal discharge Professional sports activities Complaining about another pain in the hip area according to the student Current or history of severe mental illness such as severe depression, bipolar, suicidal thoughts Consumption of psychoactive substances or alcohol and drugs Having symptoms of depression or anxiety Taking anti-depressants and anxiety medications during the study Participation in other psychological interventions such as psychotherapy, meditation, yoga The occurrence of stressful events at least six months before the start of the study

Design outcomes

Primary

MeasureTime frame
Pelvic pains. Timepoint: on the second day of the first menstrual cycle before the study and three consecutive cycles after the intervention. Method of measurement: Short-Form McGill Pain Questionnaire.;Depression. Timepoint: on the second day of the first menstrual cycle before the study and three consecutive cycles after the intervention. Method of measurement: Hospital anxiety and depression questionnaire.;Anxiety. Timepoint: on the second day of the first menstrual cycle before the study and three consecutive cycles after the intervention. Method of measurement: Hospital anxiety and depression questionnaire.

Secondary

MeasureTime frame
Menstrual distress. Timepoint: On the second day of the first menstrual cycle before the study and three consecutive cycles after the intervention. Method of measurement: Moos Menstrual Distress Questionnaire.;Pain self-efficacy. Timepoint: On the second day of the first menstrual cycle before the study and three consecutive cycles after the intervention. Method of measurement: Pain Self-efficacy Questionnaire.;Perceived stress. Timepoint: On the second day of the first menstrual cycle before the study and three consecutive cycles after the intervention. Method of measurement: Perceived Stress Scale Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHajar Adib-Rad

Babol University of Medical Sciences

Adibrad2015@yahoo.com+98 11 3219 0597

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 6, 2026