- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05132608
Effect of a Social Media-based Health Education Program on Postnatal Care (PNC) Knowledge Among Pregnant Women Using Smartphones in Dhulikhel Hospital
August 28, 2025 updated by: Kalpana Chaudhary, Kathmandu University School of Medical Sciences
Effect of a Social Media-based Health Education Program on Postnatal Care (PNC) Knowledge Among Pregnant Women Using Smartphones in Dhulikhel Hospital: a Randomized Controlled Trial
Its an interventional study conducted to assess the effect of social media-based health education program on PNC knowledge among pregnant women attending Dhulikhel hospital, Nepal.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The study is a two-arm open-label randomized controlled trial conducted among literate pregnant visiting Dhulikhel hospital for ANC check-up.
A computer-based program allocated 229 pregnant women owning smartphone with internet connectivity in a 1:1 ratio to either intervention (n=109) or usual care (n=120).
The investigators assessed PNC knowledge in the participants by interviewing in-person or via phone; questionnaire was adopted from the previous study conducted to determine the knowledge of postnatal care among postpartum mothers in Asmara; that contained 20 knowledge questions with a maximum possible score of 61.
The questionnaire was translated and pretested in Nepali, with the Cronbach alpa of 0.83.
The intervention group received a 16 minutes video developed by using Health belief model via social media and the participants were reminded to view the video every week via telephone for a month.
Control group received usual care.
The primary outcome of the study was PNC knowledge score.
The investigators utilized intent-to-treat analysis and measured the effect of the intervention on PNC knowledge score using linear regression analysis.
Study Type
Interventional
Enrollment (Actual)
229
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Bagmati
-
Dhulikhel, Bagmati, Nepal, 11008
- Kalpana Chaudhary
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- literate pregnant women
- owned a smartphone
- used social media (either What's App, Viber, or Facebook)
- had internet connectivity (WIFI or mobile data)
Exclusion Criteria:
• learning difficulties(dementia) or vision impairment
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Social Media
social media based health education program developed using Health belief model
|
The social media-based health education program consist of 16 minute PNC video in Nepali language guided by Health Belief Model.
The video provided general information on postnatal care including frequency, timing, and place providing postnatal care; danger signs of mother and newborn; different services provided at each PNC visit, and the importance of PNC visit.
The researcher sent PNC videos through instant messaging (IM) software applications such as Viber, What's App, and Facebook messenger to the intervention group.
|
|
No Intervention: Usual care
physical assessment of maternal and foetal wellbeing, screening, treatment, and receiving preventive measures
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
PNC knowledge assessment
Time Frame: 3 months
|
The investigators adopted knowledge assessment questionnaire from the hospital-based cross-sectional study conducted to determine the knowledge of postnatal care among postpartum mothers during discharge in maternity hospitals in Asmara
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Shaye R, Schwaninger B, Hoffman D. Activator construction simplified. J Clin Orthod. 1979 Nov;13(11):773-8. No abstract available.
- Chaudhary K, Nepal J, Shrestha K, Karmacharya M, Khadka D, Shrestha A, Shakya PR, Rawal S, Shrestha A. Effect of a social media-based health education program on postnatal care (PNC) knowledge among pregnant women using smartphones in Dhulikhel hospital: A randomized controlled trial. PLoS One. 2023 Jan 20;18(1):e0280622. doi: 10.1371/journal.pone.0280622. eCollection 2023.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 1, 2021
Primary Completion (Actual)
August 15, 2021
Study Completion (Actual)
August 15, 2021
Study Registration Dates
First Submitted
November 11, 2021
First Submitted That Met QC Criteria
November 23, 2021
First Posted (Actual)
November 24, 2021
Study Record Updates
Last Update Posted (Estimated)
September 5, 2025
Last Update Submitted That Met QC Criteria
August 28, 2025
Last Verified
August 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- 106/20
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.
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