The Effect of Haptonomy Practice on Body Functionality Appreciation and Childbirth Self-Efficacy in Pregnant Women

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-50
SponsorTokat Gaziosmanpasa University

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

80 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Tokat Gaziosmanpasa University

Lead sponsor

Ondokuz Mayıs University

Sponsor institution

Ondokuz Mayıs University

Collaborator