- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07462585
Impact of the Model Health Behaviour Mother 1000 Days of Life Health Online-Based on Prenatal, Intranatal, and Postnatal
The goal of this quasi-experimental interventional study is to learn whether an online-based Health Behavior Mother intervention during the first 1000 days of life can improve maternal care behavior in third-trimester pregnant women in the working area of the Pematang Jaya Community Health Center, Langkat Regency, Indonesia. The main questions it aims to answer are:
- Does the online Health Behavior Mother intervention improve maternal knowledge regarding prenatal, intranatal, and postnatal care during the first 1000 days of life?
- Does the online Health Behavior Mother intervention improve maternal attitudes regarding prenatal, intranatal, and postnatal care during the first 1000 days of life?
- Does the online Health Behavior Mother intervention improve maternal practices regarding prenatal, intranatal, and postnatal care during the first 1000 days of life?
Participants will be third-trimester pregnant women who live in the working area of the Pematang Jaya Community Health Center and agree to participate in the study.
Participants will:
- Complete a pre-test questionnaire measuring maternal knowledge, attitudes, and practices regarding care during the first 1000 days of life.
- Receive eight sessions of online health education related to prenatal care, childbirth preparation, and postnatal care.
- Participate in online discussions and monitoring through digital communication platforms.
- Complete a post-test questionnaire to evaluate changes in knowledge, attitudes, and practices after the intervention.
The intervention includes educational materials on:
- Prenatal care (ANC visits, high-risk screening, maternal and fetal nutrition, psychological preparation for childbirth)
- Intranatal care (pain management, early breastfeeding initiation, emergency management)
- Postnatal care (maternal health, lactation counseling, family planning, and newborn care)
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
North of Sumatera
-
Medan, North of Sumatera, Indonesia
- Universitas Sumatera Utara
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Pregnant women in their third trimester.
- Residing in the working area of Pematang Jaya Community Health Center.
- Willing to participate and provide informed consent.
Exclusion Criteria:
- Pregnant women not in their third trimester
- Not residing in the working area of Pematang Jaya Community Health Center.
- Unwilling to participate or unable to provide informed consent
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Model Health Behaviour Mother 1000 Days of Life Health
|
The Health Behavior Mother 1000 Days of Life intervention is an online-based health education program targeting mothers in Langkat during prenatal, intranatal, and postnatal periods.
It includes eight structured sessions delivered and monitored online, covering prenatal care (ANC, high-risk screening, fetal nutrition, psychological preparation, childbirth), intranatal care (pain management, early breastfeeding, emergency management), and postnatal care (maternal health, lactation counseling, family planning, newborn care).
Trained community leaders assist in delivering content on stunting prevention and maternal-child health.
Maternal knowledge, attitudes, and skills are assessed through questionnaires and observational tools.
The intervention aims to improve maternal health behaviors and reduce stunting risk in children during the first 1000 days of life.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from Baseline in Maternal Knowledge, Attitudes, and Practices on Prenatal, Intranatal, and Postnatal Care
Time Frame: From enrollment (third trimester of pregnancy) to 1 month postpartum, during which 8 online counseling sessions were delivered and monitored.
|
Changes in maternal knowledge, attitudes, and practices regarding prenatal to postnatal periods care before and after the eight-session online Health Behavior Mother 1000 Days of Life intervention.
Knowledge is assessed using True/False items (correct =1, incorrect =0) and converted to a percentage score (0-100), where higher scores indicate better knowledge.
Knowledge is categorized as good (76-100%), fair (65-75%), and poor (≤56%).
Attitudes are measured using a five-point Likert scale (1-5) and converted to percentages (0-100); higher scores indicate more positive attitudes (>50% positive, ≤50% negative).
Practices related to antenatal care, birth preparation, postpartum care, and breastfeeding are assessed by interview and categorized as practice or not practice.
The instrument showed good reliability (Cronbach's alpha = 0.855) and content validity through expert review.
The primary outcome is the change between baseline (third trimester) and post-intervention.
|
From enrollment (third trimester of pregnancy) to 1 month postpartum, during which 8 online counseling sessions were delivered and monitored.
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- No: 611/KEPK/USU/2025
- Talenta and Langkat (Other Identifier: University of North Sumatera)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Pregnancy
-
Far Eastern Memorial HospitalCompletedCornual PregnancyTaiwan
-
Peking Union Medical College HospitalPeking Union Medical CollegeUnknownPregnancy | Pregnancy Related | Infant | Pregnancy Disease | Risk FactorChina
-
Kafrelsheikh UniversityNot yet recruitingEctopic PregnancyEgypt
-
Meir Medical CenterRecruiting
-
Bagcilar Training and Research HospitalRecruitingEctopic PregnancyTurkey (Türkiye)
-
MELISA Institute Genomics & Proteomics Research...RecruitingHealthy | Pregnancy | Early Pregnancy | Early Pregnancy Loss | ChildbirthChile
-
Ufuk UniversityNot yet recruitingPregnancy Complications | Pregnancy Loss | Pregnancy Preterm
-
Hadassah Medical OrganizationCompleted
-
Turku University HospitalUniversity of TurkuCompleted
-
Centre Hospitalier Universitaire de Saint EtienneCompletedProlonged PregnancyFrance
Clinical Trials on the Model Health Behaviour Mother 1000 Days of Life Health Online-Based on Prenatal, Intranatal, and Postnatal
-
Istanbul University - CerrahpasaRecruiting
-
Ankara Yildirim Beyazıt UniversityCompleted
-
Biruni UniversityCompletedOveractive Bladder
-
Chinese University of Hong KongRecruitingNon Communicable Diseases | Health-risk BehavioursHong Kong
-
Memorial Sloan Kettering Cancer CenterBoehringer Ingelheim; National Comprehensive Cancer NetworkCompletedHead and Neck Cancer | Squamous Cell CancerUnited States