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Studying the effect of oral capsule of parsley on anxiety and depression in menopause women

Studying the effect of oral capsule of parsley on anxiety and depression in menopause women: A randomized triple blinded controlled trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250608066117N1
Enrollment
64
Registered
2025-06-10
Start date
2025-06-21
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Anxiety and depression in menopaused women.

Interventions

Intervention 1: Intervention group: will receive one oral capsule containing 250 mg of parsley powder twice daily, at least half an hour after breakfast and after dinner (total daily dose will be 500

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 60 Years

Inclusion criteria

Inclusion criteria: Willingness to participate in the study Having at least primary education Age 45 to 60 years No menstrual bleeding or spotting for at least the past year Mild to moderate symptoms of anxiety and depression based on the Spielberger State-Trait Anxiety Inventory and Beck Depression Inventory

Exclusion criteria

Exclusion criteria: Allergy to parsley Major depression requires specialized treatment People with thoughts of suicide and self-harm Having all known physical disorders and diseases, such as kidney, liver, heart, thyroid, bleeding diseases, malignancies, degenerative and autoimmune diseases Use of antidepressants and tranquilizers in the past 3 months Having a history of stressful events or unfortunate events in the last 6 months, such as the death of a spouse or loved one Having a history of drug and alcohol abuse Simultaneous use of medicinal herbs for any reason

Design outcomes

Primary

MeasureTime frame
Depression score on the Beck Depression Inventory. Timepoint: At the beginning of the study and weeks 4 and 8 after the intervention. Method of measurement: The Beck Depression Inventory will be used to measure depression.;Anxiety score on the Spielberger State-Trait Inventory. Timepoint: At the beginning of the study and weeks 4 and 8 after the intervention. Method of measurement: The Spielberger Trait State Inventory will be used to measure anxiety.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParastoo Daemi Mojdehi

Ahvaz University of Medical Sciences

edumaum@ajums.ac.ir+98 61 3311 0000

Outcome results

None listed

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