The Effect Of Oral Capsules Of Jujube Fruit Extract On The Prevention Of Postpartum Depressio

Recruitment & Eligibility

Status: Pending

Sex: Female

Target Recruitment: 128

Inclusion Criteria

Conscious Consent Of The Mother
Women 18-40 Years Old
Recent Pregnancy Asked
No History Of Recurrent Miscarriage Or Infertility
Resident Of Torbate Jam
Live With His Wife
On The 10th Day After Normal Delivery Without Complications (Complication: Any Obstetric Complications Such As High Blood Pressure, Diabetes Or Hospitalization Of The Mother Due To Postpartum Complications)
Having A Low-Risk Pregnancy (Low-Risk Pregnancy: A Pregnancy That Has No Potential Side Effects That Threaten The Health Of The Mother And Fetus)
Having A Mobile Phone Number
No Stress, Depression And Severe Anxiety (Depression And Severe Anxiety: Scores Of 24 And Above On The Stress Subscale And 15 And More On The Anxiety Subscale And 21 And More On The DASS-21 Questionnaire)
Score Less Than 12 On The Edinburgh Depression Test
Do Not Be Allergic To Jujube
No Accidents (Accidents Such As The Death Or Hospitalization Of A Family Member During The Last Three Months)
Do Not Currently Be Treated For Depression
Have No Medical History (Medical Conditions: Hypertension, Hypothyroidism And Parathyroidism, Heart Disease, Kidney Disease, Hypertension Under Treatment, Migraine, Epilepsy, Respiratory Disease, Hyperlipidemia, Diabetes)
Do Not Have Any Mental Illness (Mental Illness: A History Of Depression Or Neurological Disease Or Any Other Mental Disorder According To The Patient)

Exclusion Criteria

Reluctance To Continue Research
Do Not Take The Drug For Two Consecutive Days
Incidence Of Jujube Allergy
Major Stress During Study(Major Stress: Serious Illness Of Yourself Or A Spouse, Death Of A Loved One, Unemployment, Accidents And Severe Family Disputes)
Depression While Studying With A Psychiatrist Diagnosis
The Baby Has An Abnormality Or The Baby Dies
Change Of Residence During The Study
Smoking, Drinking Alcohol Or Taking Any Drugs

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Depression Score Before And After The Intervention. Timepoint: At The Beginning Of The Study And At The End Of The Second, Fourth And Sixth Weeks After Entering The Study, The Depression Score Will Be Measured. Method of measurement: Edinburgh Postpartum Depression Screening Questionnaire.

Secondary Outcome Measures

Name	Time	Method
Satisfaction With The Sex Of The Baby. Timepoint: At The Beginning Of The Study. Method of measurement: Demographic And Midwifery Profile Questionnaire.