The Effect of Mindfulness-Based Intervention and Haptonomy Application on Birth Self-Efficacy, Prenatal Attachment and Anxiety Levels of Pregnant Women With Fear of ChildBirth

Bayburt University

Status: Not yet enrolling

Conditions: Haptonomy; Attachment; Mindfulness; Fear of Childbirth; Self-Efficacy

Treatments: Other: Mindfulness Training; Other: Haptonomy Training

Study type: Interventional

Funder types: Other

Identifiers

NCT06956898

14219

Details and patient eligibility

About

Fear of childbirth is a common condition encountered during pregnancy. Women with fear of childbirth have reduced birth self-efficacy, and it leads to mental health problems in the prenatal and postnatal periods, reducing mother-infant bonding. Therefore, it is of critical importance to implement effective and applicable interventions focused on health and well-being to reduce fear of childbirth. Considering the increasing cesarean section rates today, holistic intervention strategies that can positively affect the birth experiences of pregnant women and support their psychological well-being are needed. In this sense, mindfulness and haptonomy applications, which are holistic intervention strategies, will allow us to meet the psychological and emotional needs of pregnant women with fear of childbirth and improve their birth experiences.

No study has been found in the literature that systematically evaluates the effects of a holistic intervention strategy for women with fear of childbirth during pregnancy. This study will enable the development of new and effective intervention strategies that can be used in prenatal and postnatal care practices and will guide clinical practices to make pregnant women's birth experiences more positive. In this study, the effects of mindfulness-based intervention and haptonomy application on childbirth self-efficacy, prenatal attachment and anxiety levels in pregnant women experiencing fear of childbirth will be evaluated. This research will be conducted as a randomized controlled experimental study. The data of the research will consist of 225 women (75 in the mindfulness group, 75 in the haptonomy group, and 75 in the control group) who applied to the Erzurum City Hospital Gynecology and Obstetrics Clinic between 01.06.2024 and 01.07.2025. The data will be collected face to face using the "Personal Information Form", "Wijma Childbirth Expectation/Experience Scale Version A", "Prenatal Attachment Inventory", and "State Anxiety Scale".

Enrollment: 225 estimated patients

Sex: Female

Ages: 18 to 45 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Being a primary school graduate,
• Women in their 28th week of pregnancy,
• Being primigravida,
• Women with a healthy pregnancy,
• Women with a Wijma Childbirth Expectation/Experience Scale version A score of ≥38,
• Women who agree to participate in the study and do not have any chronic health problems that would prevent them from participating.

Exclusion criteria

• Pregnant women who did not agree to participate in the study or who left the study at any stage of the study will constitute the study.

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

---

225 participants in 3 patient groups

Mindfulness Group

Experimental group

Description:

Providing mindfulness training

Treatment:

Other: Mindfulness Training

Haptonomy Group

Experimental group

Description:

Providing haptonomy training

Treatment:

Other: Haptonomy Training

Control Group

No Intervention group

Description:

No intervention will be applied to the control group.