Effectiveness of a Pregnancy Care App on Maternal Knowledge and Anxiety in Pregnant Women

NCT ID: NCT07229989

Last Updated: 2026-01-14

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

COMPLETED

Clinical Phase

NA

Total Enrollment

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-09-18

Study Completion Date

2025-12-30

Brief Summary

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

1. Objective:

To evaluate the effectiveness of the Pregnancy Care mobile application in improving maternal knowledge and reducing anxiety in preparation for childbirth, through an educational and holistic therapy-based approach.
2. Key Questions:

1. Can the Pregnancy Care app improve pregnant women's knowledge about pregnancy and childbirth preparation?
2. Is the app effective in reducing anxiety levels among pregnant women before delivery?
3. What are the changes in knowledge and anxiety levels before and after the intervention in the group using the app compared to the control group?
3. Procedure:

This study uses a quasi-experimental design with a pre-test and post-test approach involving two groups:

1. Intervention group: Participants will use the Pregnancy Care app for one week. The app includes educational content on physical and emotional changes during pregnancy, nutritional and activity needs, and childbirth preparation. It also features holistic therapy components such as antenatal yoga, acupressure, guided relaxation, meditation, self-hypnosis, mindfulness, deep breathing, journaling, and hope-based affirmations.
2. Control group: Participants will receive standard education without using the app.

Measurements will be taken before and after the intervention using validated questionnaires to assess knowledge and anxiety levels. The data will be analyzed to determine the effectiveness of the app in enhancing maternal readiness for childbirth

Detailed Description

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

Background:

Anxiety before childbirth is a common issue among pregnant women and can negatively affect the delivery process and maternal-infant health. Adequate knowledge and psychological support are essential to help mothers feel more prepared and confident.

Study Purpose:

To develop and evaluate the Pregnancy Care mobile application as a digital intervention aimed at improving maternal knowledge and reducing anxiety through educational content and holistic therapy.

App Content: The Pregnancy Care app integrates:

Educational modules covering:

Physical and emotional changes during pregnancy Nutritional and activity needs Stages of labor and delivery Pain management and breathing techniques Postpartum care and breastfeeding

Holistic therapy features:

Body: Antenatal yoga, acupressure, massage points Mind: Guided relaxation, meditation, self-hypnosis, mindfulness, deep breathing Soul: hope affirmations, spiritual and motivational content

Study Design:

A quasi-experimental design with two groups:

Intervention group: Uses the pcycare for 21 day Control group: Receives standard education without the pcycare

Measurement and Analysis:

Pre-test and post-test assessments are conducted using validated questionnaires to measure maternal knowledge and anxiety levels. Data are analyzed to determine the effectiveness of the app in improving childbirth preparedness.

Conditions

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

Pregnancy

Study Design

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

Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

This study uses a quasi-experimental design with a pre-test and post-test approach. Participants are assigned to one of two groups: an intervention group using the Pregnancy Care app for 21 day, and a control group receiving standard education. The study aims to evaluate the app's effectiveness in improving maternal knowledge and reducing anxiety before childbirth.
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

This study does not involve masking or blinding. All participants and investigators are aware of the group assignments and the intervention being used.

Study Groups

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

Intervention Group

Arm Type: Experimental Arm Name: Intervention Group Description: Participants in this group will use the pcycare digital for 21 day The app includes educational content and holistic therapy.

Group Type EXPERIMENTAL

PcyCare (Pregnancy Care) App

Intervention Type BEHAVIORAL

The Pregnancy Care App is a mobile-based self-learning platform designed to improve maternal knowledge and reduce anxiety before childbirth. It includes educational modules on pregnancy and labor preparation, as well as holistic therapy features such as antenatal yoga, acupressure, guided relaxation, meditation, self-hypnosis, mindfulness, deep breathing, journaling, and hope-based affirmations. Participants in the intervention group will use the app for two week.

control group

Arm Type: Active Comparator Arm Name: Control Group Description: Participants in this group will receive standard maternal education without using the mobile application.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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

PcyCare (Pregnancy Care) App

The Pregnancy Care App is a mobile-based self-learning platform designed to improve maternal knowledge and reduce anxiety before childbirth. It includes educational modules on pregnancy and labor preparation, as well as holistic therapy features such as antenatal yoga, acupressure, guided relaxation, meditation, self-hypnosis, mindfulness, deep breathing, journaling, and hope-based affirmations. Participants in the intervention group will use the app for two week.

Intervention Type BEHAVIORAL

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Mobile Health for Maternal Education Digital Holistic Therapy for Pregnancy

Eligibility Criteria

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

Inclusion Criteria

1. Pregnant women aged 20-40 years
2. Gestational age between 28 and 35 weeks
3. Able to read and understand the language used in the PcyCare platform
4. Owns a smartphone, tablet, or computer with internet access
5. Provides informed consent to participate

Exclusion Criteria

1. High-risk pregnancy requiring intensive medical care
2. Severe psychiatric or cognitive disorders that would prevent platform use
3. Participation in another conflicting educational or intervention study
Minimum Eligible Age

20 Years

Maximum Eligible Age

35 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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

Lincoln University College Malaysia

OTHER

Sponsor Role lead

Responsible Party

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

Nurul Jannah, M.Tr.Keb

Principle Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Nurul Jannah, M.Tr.Keb

Role: PRINCIPAL_INVESTIGATOR

Lincoln University College Malaysia

Locations

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

Disctrict

Semarang, Central Java, Indonesia

Site Status

Countries

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

Indonesia

Other Identifiers

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

LUC_02_Jannah

Identifier Type: OTHER

Identifier Source: secondary_id

LUC_02_Jannah

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

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