Skip to content

The effect of Ocimum Basilicum on postpartum depression

The effect of Ocimum Basilicum capsule on postpartum depression symptoms: A Randomized Controled Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220926056046N2
Enrollment
78
Registered
2023-02-21
Start date
2023-03-14
Completion date
Unknown
Last updated
2023-03-13

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

Conditions

postpartum depression. Mood disorder due to known physiological condition with depressive features

Interventions

Intervention 1: Intervention group: Participants in the intervention group will receive 2 capsules of 500 mg containing dried green basil leaf powder daily for eight weeks. Intervention 2: Control gro

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 49 Years

Inclusion criteria

Inclusion criteria: Having a vaginal term birth or cesarean section Having a healthy baby Being literate in reading and writing

Exclusion criteria

Exclusion criteria: Obtaining a score of 13 and above in the Edinburgh Questionnaire Mental retardation Chronic diseases aggravated during pregnancy Occurrence of a stressful event such as death or diagnosis of an incurable disease in first-degree family members, divorce, within three months. Before starting the study

Design outcomes

Primary

MeasureTime frame
Postpartum depression score. Timepoint: Before the start of the intervention and the end of the eighth week after the start of the intervention. Method of measurement: Edinburgh depression questionnaire.

Secondary

MeasureTime frame
Postpartum sleep quality score. Timepoint: The end of the eighth week after the start of the intervention. Method of measurement: Postpartum sleep quality questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMonireh Abdi

Tabriz University of Medical Sciences

m85438a@gmail.com+98 903 818 5438

Outcome results

None listed

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