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Effect of Cognitive Behavioral Therapy on premenstrual syndrome

Effects of Cognitive- Behavioral Therapy on Health Related Quality of Life of Females with Premenstrual Syndrome

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015062822960N1
Enrollment
40
Registered
2015-10-21
Start date
2015-07-31
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Premenstrual Syndrome. Premenstrual tension syndrome

Interventions

Intervention 1: Intervention group: Participants in the intervention group, will receive ten weekly 90-minute group cognitive-behavioral therapy sessions (each session, 90 minutes ). The intervention
Treatment - Other
Intervention group: Participants in the intervention group, will receive ten weekly 90-minute group cognitive-behavioral therapy sessions (each session, 90 minutes ). The intervention will consist of
control group: The subjects of control group received no interventions until the end of the study

Sponsors

Vicechancellor for research, Shahid Chamran University of Midical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: having regular menstrual cycles (24-35days); do not taking hormonal, psychotropic, vitamins, oral contraceptives at the time; not being pregnant or lactating; not experiencing stressors such as marriage, surgery, death of relatives, and etc. during the previous three months; not being under any kind of treatment to relieve the symptoms during the study and not having internal, gynecological, and psychiatric disorders. Exclusion criteria: Absence of the above conditions.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Health Related Quality of Life. Timepoint: Before intervention, 70 days after the start of intervention, 2month after the end of intervention. Method of measurement: Health Related Quality of Life Questionaire.

Secondary

MeasureTime frame
Premenstrual Syndrome. Timepoint: before intervention, 70 days after the start of intervention, 2 month after the end of intervention. Method of measurement: Daily Record of Severity of Problems.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Izadi-Mazidi

Shahed University

Maryam.izadi.psy@gmail.com+98 215121362

Outcome results

None listed

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