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Dried black seed grape(vitis vinifera) effect on premenstrual syndrom treatment process

Effect of dried black seed grape (vitis vinifera) on clinical and mood symptom in Students with premenstrual syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015073116123N6
Enrollment
200
Registered
2015-10-24
Start date
2015-10-23
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 syndrom. Premenstrual tension syndrom

Interventions

Intervention 1: Intervention group: Diet controlling
dried black seed grape 90 gram per day, during 7 days before menses, for 2 months. Intervention 2: Control group: Diet controlling, for 2 months.
Treatment - Other
Intervention group: Diet controlling
dried black seed grape 90 gram per day, during 7 days before menses, for 2 months.
Control group: Diet controlling, for 2 months.

Sponsors

Vice Chancellor for Research and Technology,Ahvaz Jundishapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria:age 18-35; residence in dormitory; The risk of moderate and severe forms; The lack of any specific tratment to treat PMS; Regular menstrual cycles every 24 to 35 days; Lack of reproductive system diseases; Non-marital. Exclution criteria:Physical and mental stress in the last three months; Physical illness or medication Consumption; A history of mental illness; Consumption of Antidepressants in recent months; Hormone therapy; Supplements; Having a regular exercise; any specific treatment to treat PMS; Failure to use 80% dried black seed grape during the intervention.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Physical symptom score. Timepoint: Befor and first and second month end of intervention period. Method of measurement: Rossignol and Bonnlander standard questionnaire.;Mood symptom score. Timepoint: Befor and first and second month end of intervention period. Method of measurement: Rossignol and Bonnlander standard questionnaire.;Psychical symptom score. Timepoint: Befor and first and second month end of intervention period. Method of measurement: Rossignol and Bonnlander standard questionnaire.

Secondary

MeasureTime frame
Physical acyivity score. Timepoint: First month and second month after intervention. Method of measurement: International physical activity questionnaire.;Macro nutrients intake. Timepoint: First month and second month after intervention. Method of measurement: 3-day 24-hour recall.;Weight. Timepoint: Before and first and second end of intervention period. Method of measurement: Balance.;Height. Timepoint: Before and first and second end of intervention period. Method of measurement: Stadiometer.;Waist circumference. Timepoint: Before and first and second end of intervention period. Method of measurement: Tape measure.;Hip circumference. Timepoint: Before and first and second end of intervention period. Method of measurement: Tape measure.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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