Clinical Trials Logo

Clinical Trial Summary

A total of 36 volunteers of postpartum women within 7 days with significant breast engorgement, will be recruited in China Medical University Hospital, Taichung, Taiwan. The participants will be randomly assigned into 3 groups, each of 12 people, namely, routine care group, routine care plus electrical-acupuncture experiment group, and routine care plus transcutaneous electrical nerve stimulation group.


Clinical Trial Description

Participants will receive once a day, three consecutive days of interventions in each group, including identical routine care. On each visit, severity index (SI) subject to the extent of erythema, tension and pain over breast will be assessed. Questionnaires of Breastfeeding Self-Efficacy Scale (BSES-SF) and of Edinburgh postnatal depression scale (EPDS) will be performed. Heart-rate variability was evaluated and recorded via a real-time handheld HRV device. Oxycontin, Cortisol, sodium and potassium levels in breastmilk will be tested . A telephone follow-up will be performed in 30 days after completion of treatment, and the data will be collected and analyzed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04998565
Study type Interventional
Source China Medical University Hospital
Contact
Status Terminated
Phase N/A
Start date September 12, 2017
Completion date July 31, 2019

See also
  Status Clinical Trial Phase
Completed NCT03665038 - A Study to Assess the Safety of Brexanolone in the Treatment of Adolescent Female Participants With Postpartum Depression (PPD) Phase 3
Recruiting NCT06042972 - Risk of Maternal Depression From 1 Year to 4 Years Postpartum in Yvelines
Completed NCT04813341 - Effectiveness of Mat Pilates and Aerobic Training on Fatigue and Depression N/A
Completed NCT04135612 - The Impact of a Daily Smartphone-based Communication Among Postpartum Women on Breastfeeding Rates N/A
Recruiting NCT05595486 - Baby2Home (B2H) Mobile Health Application N/A
Not yet recruiting NCT04516668 - Effect of Tele-consultation in Addition With Psychiatric Follow-up During COVID-19 in Women Who Have Medical History of Post-partum Depression
Completed NCT05215028 - Optimization of Mother-child Dyad Follow-up by a Multidomain Application: Real-world Cross Sectional Study
Recruiting NCT04129476 - Effect of a Cooperative Education Program Based on Precede-Proceed Model During Pregnancy on Postpartum Depression N/A
Recruiting NCT04193462 - Relationship-Based Intervention for Post-Partum Depression N/A
Completed NCT03638687 - Neuroimaging Epigenetics of Prospective Postpartum Depression Biomarkers
Active, not recruiting NCT03052374 - Video-Feedback Interaction Guidance for Improving Interactions Between Depressed Mothers and Their Infants ("VID-KIDS") N/A
Active, not recruiting NCT04940585 - ROSE in Sunset Park N/A
Terminated NCT04011592 - Efficacy And Tolerability Of Sub-Anesthetic Ketamine In Postpartum Depression Phase 2
Recruiting NCT05887115 - Nurse Family Partnership for Women With Previous Live Births N/A
Completed NCT04818047 - Adaptation and Pilot Testing of Web and Mobile Interface for the VID-KIDS Intervention N/A
Not yet recruiting NCT05643898 - "Mamá, te Entiendo" App-based Intervention for Reducing Depressive Symptoms in Postpartum Women N/A
Terminated NCT04264520 - Initial Intervention Efficacy for an Online PTSD Intervention for Pregnant Women N/A
Recruiting NCT04845347 - A Wearable Morning Light Treatment for Postpartum Depression N/A
Enrolling by invitation NCT05186272 - mHealth Mindfulness Intervention for Pregnant Black and Latina Women at Risk of Postpartum Depression Phase 3
Completed NCT04087317 - Vaginal Postpartum Pain Management Protocol Comparison N/A