About this trial
Study Type and Aim:
This clinical study aims to examine the effects of haptonomy practices on appreciation of bodily functionality and childbirth self-efficacy among healthy pregnant women. The study seeks to determine whether haptonomy can enhance these two outcomes.
Key Research Questions:
Do haptonomy practices increase appreciation of bodily functionality in pregnant women? Do haptonomy practices increase childbirth self-efficacy in pregnant women?
Comparison:
Researchers will compare an intervention group receiving haptonomy sessions with a control group receiving only routine prenatal care to evaluate the effects of the intervention.
Participants will:
Participants will provide written informed consent to take part in the study. Pregnant women in the intervention group will attend four haptonomy sessions, each lasting approximately 45 minutes and held at 7-day intervals. Sessions will include practices to enhance body awareness, relaxation techniques, connecting with the baby, and affirmations supporting bodily functionality and childbirth self-efficacy.
Pregnant women in the control group will receive routine prenatal care and follow-up only.
All participants will complete pretest and posttest measures assessing appreciation of bodily functionality and childbirth self-efficacy.
Keywords: Haptonomy, Vaginal birth, Pregnancy, Prenatal care, Body functionality appreciation, Birth self-efficacy
Eligibility criteria
Qualifiers
Aged 18 years or older
Spontaneous pregnancy at 28 weeks of gestation
Primiparous (first pregnancy)
Able to read and write in Turkish
Disqualifiers
Any health problems in the mother or fetus
History of complications during pregnancy
Diagnosed psychiatric disorders or use of psychiatric medication
Any physical, mental, or cognitive disabilities
Trial design
Treatments tested in this trial
- Haptonomy
Treatment groups
Sponsors and collaborators
Tokat Gaziosmanpasa University
Lead sponsor
Ondokuz Mayıs University
Sponsor institution
Ondokuz Mayıs University
Collaborator