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Influence of the implementation of Leventhal self-regulation model on Illness perception and pain severity of primary dysmenorrhea

Influence of the implementation of Leventhal self-regulation model on Illness perception and pain severity of primary dysmenorrhea

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190625044002N2
Enrollment
120
Registered
2020-01-06
Start date
2020-01-21
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

Primary dysmenorrhea. Primary dysmenorrhea

Interventions

Intervention 1: Intervention group: Training based on Leventhal self-regulation model. Based on the Leventhal self-regulation model and based on the results obtained from subscales of questionnaires c

Sponsors

Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
14 Years to 19 Years

Inclusion criteria

Inclusion criteria: The resident of Qazvin Have regular menstruation Experience at least 2 years of menstruation Severity of pain in menstruation 4 or more than 4 Enroll in high school Ages 14 to 19 years old

Exclusion criteria

Exclusion criteria: The presence of secondary dysmenorrhoea and its underlying causes History of known mental illnesses Substance abuse history (self-declaration) Surgical history of women Unwilling to participate in the study. Being Married Mandatory drug use in the last 6 months Not attending meetings (attendance at all meetings is obligatory)

Design outcomes

Primary

MeasureTime frame
Pain intensity of primary dysmenorrheal. Timepoint: Measurement of menstrual pain intensity one and two months before the intervention, one month and three months after the intervention. Method of measurement: Measurement of menstrual pain with visual analog scale for pain.

Secondary

MeasureTime frame
Illness Perception. Timepoint: Measurement of Illness Perception before the intervention, one month and three months after the intervention. Method of measurement: Illness Perception Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSomayeh Asgari

Qazvin University of Medical Sciences

s.asgari71@gmail.com+98 28 3333 6003

Outcome results

None listed

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