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NCT04923698 Clinical Trial

Effect of Yoga on Postpartum Depression

Yoga Clinical Trial

Official title:
Yoga on Postpartum Depression

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04923698
Other study ID # Cairo Un110
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 24, 2019
Est. completion date March 30, 2020

Study information
Verified date June 2021
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study was conducted to investigate the effect of yoga on postpartum depression. Subjects: Forty primipara women with postpartum depression (PPD) selected randomly from Kasr El Ainy University Hospital in Cairo complaining of postpartum depression at least one month after childbirth shared in this study.

Description:

This study was conducted to investigate the effect of yoga on postpartum depression. Subjects: Forty primipara women with postpartum depression (PPD) selected randomly from Kasr El Ainy University Hospital in Cairo complaining of postpartum depression at least one month after childbirth shared in this study. Group A (Control group): It consisted of 20 women and treated by antidepressant drugs only for 12 weeks. Group B (Study group): It consisted of 20 women and treated by the same antidepressant drugs as in group A and yoga program, 50 minutes daily,7 days per week for 12 weeks (Total 84 sessions).

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date March 30, 2020
Est. primary completion date March 30, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Their ages were ranged from 20-35 years - Their body mass index was less than 30 kg/m2 Exclusion Criteria: - cardiac arrhythmia, - respiratory problems, - uncontrolled Type I diabetes

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• yoga training
All women in group B were treated by the same antidepressant drugs as in group A and yoga program, 50 minutes daily, 7 days per week for 12 weeks (Total 84 sessions).

Locations
Country Name City State
Egypt Ghada Ebrahim Elrefaye Giza

Sponsors (1)
Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary BMI assessment The weight and height of each woman in both groups (A & B) were measured three months
Secondary Zung self-rating depression scale There are ten positively worded and ten negatively worded questions. Each question is scored on a scale of 1 through 4 three months
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