The effectiveness of happiness training on quality of life and negative and positive affection in women with premenstrual syndrome

Study of the effectiveness of happiness training on quality of life and negative and positive affection in women with premenstrual syndrome: a randomized controlled clinical trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20120718010324N47

Enrollment

Registered

2018-12-08

Start date

2018-10-31

Completion date

Unknown

Last updated

2019-01-14

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: For the intervention group, eight 120-minute sessions of group counseling once a week will be provided. Intervention 2: The control group will receive routine cares.

Eligibility

Sex/Gender

Female

Age

15 Years to 48 Years

Inclusion criteria

Inclusion criteria: Women who have symptoms of premenstrual syndrome Having age between 15 to 48 Having at least secondary education Having a normal menstrual cycle (21-35 days).

Exclusion criteria

Exclusion criteria: History of physical illness Taking psychoactive drugs Suffering from personality disorder and mood disorders

Design outcomes

Primary

Measure	Time frame
Negative and positive affection. Timepoint: Before intervention, eight weeks after the intervention. Method of measurement: Negative and positive affection questionnaire.;Quality of life. Timepoint: Before intervention, eight weeks after the intervention. Method of measurement: Quality of life questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHajizadeh Khadije

Tabriz University of Medical Sciences

hajizade_k@yahoo.com+98 41 3479 6770

Outcome results

None listed

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