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Comparative investigation of the effect of Fenugreek seed - flax seed and soy on the severity of depression at menopause

Comparative investigation of the effect of Fenugreek seed - flax seed and soy on the severity of depression at menopause

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT201110262545N2
Enrollment
120
Registered
2012-04-18
Start date
2009-09-16
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

Depression. Depressive episode

Interventions

Intervention 1: Participants in first group by 6 grams of Fenugreek daily for 8 consecutive weeks, every day will be taken orally. Intervention 2: Participants in second group by 25 grams of flaxseed
Treatment - Drugs
Participants in first group by 6 grams of Fenugreek daily for 8 consecutive weeks, every day will be taken orally
Participants in second group by 25 grams of flaxseed daily for 8 consecutive weeks, every day will be taken orally
Participants in third groups by 25 grams of Soy daily for 8 consecutive weeks, every day will be taken orally
Participants in Control group by 25 grams of Sorbitol daily for 8 consecutive weeks, every day will be taken orally .

Sponsors

Vice chancellor for research Arak University of Medical Sciences.
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: amenorrhea during the previous 12 months; with reporting menopausal depression; normal blood pressure; without use of estrogen and progesterone; without use anti depressant and anti anxiety drugs during the previous 6 months; without use of anticoagulants and NSAIDs for example ibuprofen; with out history of asthma and allergy. Exclusion criteria:Incorrect use of herbal plants; home change; skin irritation .

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Depression score. Timepoint: before intervention and two months after. Method of measurement: Beck depression questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNaimeh Akbaritorkestani

Arak University of Medical Sciences

tnaimeh@yahoo.com+98 86 1417 3501

Outcome results

None listed

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