MBSR and NLP, Postpartum Breastfeeding and Depression
Recruiting · NCT06628986 · Interventional (participants receive a specific treatment) · Lead sponsor: Aysegul Kilicli
View the official record on ClinicalTrials.gov →Interventions studied
MBSRNLPcontrol
What this trial is about
The postnatal period is a risky period in which mothers experience regressive and progressive changes and rapid biopsychosocial changes. Since this process affects not only the mother but also the family, mothers are under intense stress due to adaptation to the changes that occur in this period.
Who can take part
Age range
19 Years to 35 Years
Sex
Female
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- 19-35 years old
- caesarean section
- primiparous
- breastfeeding women
Exclusion criteria
- women who refused to participate in the research.
Where it is running
1 location listed.
- Şanlıurfa training and research hospital - Sanliurfa, Eyalet/Yerleşke, Turkey (Türkiye)