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

This trial accepts healthy volunteers

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

Design model

Parallel

Treatments tested in this trial

  • Haptonomy

    Behavioral

    Pregnant participants will receive a four-session haptonomy intervention, each lasting approximately 45 minutes. The sessions aim to enhance body awareness, reduce childbirth-related anxiety, and support birth self-efficacy. The intervention includes breathing exercises, relaxation techniques, and activities promoting maternal-fetal interaction.

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: Haptonomy InterventionExperimental treatment 1 intervention
Group B: ControlNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

The sociodemographic characteristics of the participants and their homogeneous distribution according to the experimental and control groups

Pregnancy Introductory Form: The pregnancy introductory form, developed based on the literature, was designed to evaluate the demographic and obstetric characteristics of individuals during pregnancy, their birth preferences, fears, social support status, and similar factors. The form consists of a total of 15 questions.

Time frame
baseline
2

Body Functionality Appreciation Scale:

This unidimensional 7-item scale measures individuals' appreciation of their body's functionality. It evaluates psychological aspects such as body functionality awareness, body positivity, and body acceptance. The scale is scored on a 5-point Likert scale (1=Strongly disagree, 5=Strongly agree), with total scores ranging from 7 to 35. Higher scores indicate a greater level of appreciation and respect for what one's body can do. The Turkish adaptation reported a Cronbach's alpha of 0.83.

Time frame
12 weeks
3

Birth Self-Efficacy Inventory:

This inventory measures self-efficacy levels during labor. It consists of two subscales: outcome expectancy (OE) and efficacy expectancy (EE), each containing 16 items. Total scores range from 32 to 320. Responses are rated on a 1-10 Likert scale. In the OE subscale, 1 means "not at all useful" and 10 means "very useful." In the first 13 items of the EE subscale, 1 means "completely sure" and 10 means "not at all sure," while items 14-16 are scored in reverse: 1 means "not at all sure" and 10 means "completely sure." Items 1-13 of the EE subscale are reverse-scored. The overall Cronbach's alpha reliability coefficient of the inventory is 0.82.

Time frame
12 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Tokat Gaziosmanpasa University

Lead sponsor

Ondokuz Mayıs University

Sponsor institution

Ondokuz Mayıs University

Collaborator

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