Mindfulness and neurolinguistic programs for postpartum mothers
the Effect of MBSR and NLP Applications on Fatigue, Sleep Quality, Lactation and Postpartum Depression in the Postpartum Period After Caesarean Section
This study is testing if mindfulness and neurolinguistic programming can help new mothers who had a C-section feel better and manage issues like fatigue and postpartum depression.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 90 (estimated) |
| Ages | 19 Years to 35 Years |
| Sex | Female |
| Sponsor | University of Gaziantep Academic / other |
| Locations | 1 site (Sanliurfa, Eyalet/Yerleşke) |
| Trial ID | NCT06628986 on ClinicalTrials.gov |
What this trial studies
This study investigates the effects of mindfulness-based stress reduction (MBSR) and neurolinguistic programming (NLP) on postpartum mothers who have undergone a caesarean section. It aims to address common issues such as fatigue, sleep disturbances, breastfeeding challenges, and postpartum depression. By implementing these interventions, the study seeks to improve the overall well-being of mothers during the critical postnatal period. The research will compare outcomes between those receiving the interventions and a control group.
Who should consider this trial
Good fit: Ideal candidates for this study are women aged 19-35 who have had a caesarean section and are first-time mothers currently breastfeeding.
Not a fit: Patients who are not breastfeeding or who have refused to participate in the research may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the mental and physical health of postpartum mothers, improving their breastfeeding experience and reducing depression.
How similar studies have performed: While the specific combination of MBSR and NLP for postpartum issues is novel, similar approaches have shown promise in addressing mental health and breastfeeding challenges in other populations.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 19-35 years old * caesarean section * primiparous * breastfeeding women Exclusion Criteria: * women who refused to participate in the research.
Where this trial is running
Sanliurfa, Eyalet/Yerleşke
- Şanlıurfa training and research hospital — Sanliurfa, Eyalet/Yerleşke, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: AYŞEGÜL KILIÇLI, Dr.
- Email: aysegul_ay_9@hotmail.com
- Phone: 04143181717
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.