NCT07639164Not yet recruiting
Stronger Together: Antenatal Depressive Symptoms - Prevalence and Digital Treatment
Source: ClinicalTrials.gov · Last updated 10 Jun 2026
Brief summary (registry, in English)
The main objective of the current research project is to evaluate the usability, satisfaction of the antenatal iCBT program including telephone coaching for antenatal and postnatal depressive symptoms and collect nationally representative data on population-based screening of antenatal depressive and anxiety symptoms. The overarching hypothesis is that iCBT, with easy access and affordability, is user friendly and well accepted. In addition to examining the treatment response by questionnaires, we will study the infant development comprehensively as well as potential physiological changes associated with antenatal depression or its treatment.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 1000 (estimated)
- First submitted
- 5 Jun 2026
- Start date
- 1 Aug 2026
- Primary completion date
- 30 Dec 2030
- Lead sponsor
- University of Turku
- Diseases
- Depression
- NCT number
- NCT07639164
What you commit to
- Study type: Interventional
- Planned participants: 1000
- From 1 Aug 2026 to the primary completion date, 30 Dec 2030
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study design.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- lifetime history of psychotic disorder (e.g. schizophrenia, schizoaffective disorder, bipolar disorder, psychotic depression)
Other
- active suicidal ideation
- severe substance abuse or dependence
- participates in another intervention study aiming at treating the symptoms of antenatal depression
Who the study is looking for
- fluent in written and spoken Finnish or Swedish
- access to computer or mobile phone with internet
- between 12 and 22 weeks pregnant
- screening and baseline score on the EPDS ≥10 points
Age in the registry: 18 years to 55 years · Sex: Female · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University Of Turku Coordinator of this site? Confirm its status | Turku | Finland | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.