Meditation in Early Labor: Impact on Self-Efficacy and Childbirth Fear in First-Time Mothers

NCT ID: NCT07201220

Last Updated: 2025-10-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-07-01

Study Completion Date

2025-10-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Aim-Introduction:

The feeling of uncertainty about what will happen during labor, and the mother's perception of inadequacy regarding childbirth, can lead to anxiety and stress in some pregnant women, resulting in fear of childbirth and avoidance behaviors. This study was conducted to examine whether there are significant differences in childbirth self-efficacy and fear of childbirth between primiparous pregnant women who practiced meditation and those who did not during the first stage of labor.

Materials and Methods:

This experimental study is planned to be conducted between 01.04.2025 and 01.08.2025 with a total of 60 pregnant women (30 in the experimental group and 30 in the control group) who applied to the delivery unit of a tertiary hospital in Turkey and were in the first stage of labor. After informing the pregnant women about the study and the procedures to be implemented, written informed consent was obtained from those who agreed to participate. Subsequently, the pre-tests of the relevant scales and the data collection form were administered. The relaxation meditation during childbirth was applied to the experimental group, followed by the post-tests of the same scales.

Data were collected using the "Childbirth Self-Efficacy Inventory Short Form" and the "Wijma Delivery Expectancy/Experience Questionnaire (W-DEQ) Version A." Descriptive statistics and hypothesis tests will be used for data analysis.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Introduction:

This study aims to examine whether there are significant differences in childbirth self-efficacy and fear of childbirth between primiparous pregnant women who practice meditation (experimental group) and those who do not (control group) during the first stage of labor. Childbirth is a physiological process for every woman, but feelings of uncertainty, perceived inadequacy, anxiety, and stress can lead to fear of childbirth and avoidance behavior. Studies show that 6.3-75% of pregnant women experience fear of childbirth, with 6-10% affected severely. This fear can be influenced by biological, psychological, social, and secondary factors such as previous traumatic experiences or negative birth stories. Furthermore, gestational age and parity also play important roles in the emergence of birth fear.

Fear of childbirth can result in complications such as prolonged labor, emergency or elective cesarean delivery, postpartum depression, post-traumatic stress disorder, and disruption in mother-infant bonding. Various methods, including cognitive-behavioral techniques, psychoeducation, and relaxation therapies like hypnobirthing, are used to manage this fear. Research suggests that birth fear is not solely linked to pain or information deficits but to many other factors, including a woman's sense of self-efficacy.

Self-efficacy refers to a person's belief in their ability to complete tasks or overcome challenges. A woman with high self-efficacy is more likely to manage stress-inducing situations, such as labor, by trusting her own capabilities. Increasing self-efficacy and reducing fear of childbirth can be achieved through relaxation techniques, one of which is meditation. Meditation involves mental training that helps individuals find strength and solutions to problems, promoting relaxation that may alleviate both mental and physical tension. During pregnancy and labor, meditation can assist in reducing anxiety and enhancing positive birth experiences.

Aim:

The study aims to investigate whether relaxation through meditation in the first stage of labor can enhance self-efficacy and reduce fear of childbirth in primiparous women, contributing to a less stressful and anxious labor process. Gestational age and parity are known to influence childbirth fear. The research will evaluate whether meditation can help reduce anxiety and foster self-efficacy, aiding in a more manageable birth experience.

Research Problem:

Does a significant difference exist between the self-efficacy and fear of childbirth of primiparous women who receive meditation during the first stage of labor and those who do not?

Keywords: Primiparous pregnancy, Meditation, Childbirth Self-Efficacy, Fear of Childbirth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Meditation

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

After informing the pregnant women about the study and the procedures to be implemented, informed consent will be obtained from those who agree to participate. Following this, participants will complete the data collection form, and pre-test questionnaires will be administered. Subsequently, relaxation meditation will be played via headphones during labor, and the questionnaires will be applied again as post-tests.
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

A Randomized Controlled Experimental Study

Experimental Group:

30 primiparous women in the first stage of labor receive relaxation meditation during labor. Pre- and post-tests using the Childbirth Self-Efficacy Inventory Short Form and W-DEQ Version A are applied. Data collected between 01.04.2025 and 01.08.2025 at a tertiary hospital in Turkey.

Control Group:

30 primiparous women in the first stage of labor receive standard care without intervention. The same pre- and post-tests are applied. Data collected in the same period and setting.

Group Type EXPERIMENTAL

meditation

Intervention Type BEHAVIORAL

The study is planned to include 60 pregnant women (30 in the experimental group and 30 in the control group) in the first stage of labor. After informing the participants about the study and obtaining informed consent, pre-test scales will be administered. Relaxation meditation will be applied during labor for the experimental group, followed by post-test scales.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

meditation

The study is planned to include 60 pregnant women (30 in the experimental group and 30 in the control group) in the first stage of labor. After informing the participants about the study and obtaining informed consent, pre-test scales will be administered. Relaxation meditation will be applied during labor for the experimental group, followed by post-test scales.

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

Primiparous pregnant women

In the first stage of labor

Singleton pregnancy

Aged 18 and above

Able to provide informed consent

No high-risk pregnancy or psychiatric diagnosis

Exclusion Criteria

Multiparous women

High-risk pregnancy

Previous experience with meditation during labor

Communication difficulties
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Seyhan District Health Directorate, Adana

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

EMEL SALCAN

PHD Midwife

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Seyhan İlçe Sağlık Müdürlüğü

Adana, Adana, Turkey (Türkiye)

Site Status RECRUITING

Seyhan İlçe Sağlık Müdürlüğü

Seyhan, Adana, Turkey (Türkiye)

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

EMEL SALCAN

Role: primary

05061727755

EMEL SALCAN

Role: primary

05061727755

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2022.03.06/123

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.