Home-based Transcranial Direct Current Stimulation in Postpartum Depression: the Feasibility Study and Pilot Study
Launched by ANA GANHO ÁVILA · Sep 7, 2021
Trial Information
Current as of June 26, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial is looking at a new way to help new mothers who are experiencing postpartum depression (PPD), which is a type of depression that can occur after giving birth. The study will test a method called home-based Transcranial Direct Current Stimulation (tDCS). This method uses a gentle electric current applied to the scalp to help improve brain function and mood. Researchers want to see if using tDCS at home, combined with online support and telehealth services, can effectively help mothers with PPD.
To take part in this trial, women between the ages of 18 and 45 who have experienced moderate to severe depression after having a baby may be eligible. Participants should not be taking any medication for their depression and must have had a healthy delivery. Those who have previously used tDCS or have other serious mental health issues may not qualify. If you join the study, you can expect to use the tDCS device at home while also receiving support through an online system. This research aims to collect information that could lead to a larger trial in the future to confirm the effectiveness of this approach for treating postpartum depression.
Gender
FEMALE
Eligibility criteria
- Inclusion Criteria:
- • Medication-free women with moderate to severe MD episode according to the Montgomery Asberg Depression Rating Scale (MADRS\>7), and peripartum onset, diagnosed before delivery or between the second week and month 6 postpartum
- • Between 18-45 years of age
- • Pregnancy to term
- • Uncomplicated delivery to a healthy newborn
- • Must be able to manage the technical aspects of the intervention.
- Exclusion Criteria:
- • tDCS contraindications
- • Previous experience with tDCS
- • Mental health disorder other than unipolar depression or anxiety
- • Suicidal ideation.
About Ana Ganho ávila
Ana Ganho Ávila is a dedicated clinical trial sponsor committed to advancing medical research through innovative study designs and rigorous methodologies. With a focus on enhancing patient outcomes, the organization collaborates with healthcare professionals and research institutions to conduct high-quality clinical trials across various therapeutic areas. Their expertise encompasses protocol development, regulatory compliance, and data management, ensuring that each study adheres to the highest ethical standards. By prioritizing patient safety and scientific integrity, Ana Ganho Ávila aims to contribute significantly to the development of new therapies and improve healthcare solutions.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Patients applied
Trial Officials
Ana Ganho-Ávila, PhD
Principal Investigator
University of Coimbra
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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