ClinicalTrials.gg
Not yet recruitingNCT07890077GEMPOUpdated Oct 22, 2026

Effectiveness of GEMPO E-Education on Fathers' Self-Efficacy and Ability in Newborn Care

An interventional study of GEMPO Electronic Education in Fathers' Self-Efficacy and Ability in Newborn Care, sponsored by Musnaini Musnaini. Not yet recruiting at 1 site in Indonesia. Open to male participants, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-22.

Sponsored by Musnaini Musnaini · Not applicable, Interventional, and Other

Updated Oct 22, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Sex
Male
01

Study summary

This study aims to evaluate the effectiveness of GEMPO (Holding, Bathing, and Diaper Changing) e-education on fathers' self-efficacy and ability to care for newborns. The study will involve fathers of newborns aged 0-28 days. Fathers in the intervention group will receive GEMPO e-education, while fathers in the control group will receive routine or standard health education. Self-efficacy and newborn care abilities will be measured before and after the intervention. The findings are expected to provide information on the role of electronic education in supporting fathers' involvement and skills in newborn care.

Read the detailed description

This study will evaluate the effectiveness of GEMPO (Holding, Bathing, and Diaper Changing) e-education on fathers' self-efficacy and ability in newborn care.

The study will use a Cluster Randomized Controlled Trial design with a pretest-posttest control group. The study will be conducted in four community health centers in Pekanbaru, Riau, Indonesia: Puskesmas Rumbai, Puskesmas Rumbai Bukit, Puskesmas Umban Sari, and Puskesmas Karya Wanita.

The study population will consist of fathers who have newborns aged 0-28 days and meet the eligibility criteria. The health centers will be randomly allocated to the intervention or control group. Participants in the intervention group will receive GEMPO e-education covering holding, bathing, and diaper changing for newborns. Participants in the control group will receive routine or standard education provided by the health facilities without the GEMPO e-education video.

Fathers' self-efficacy and ability in newborn care will be assessed before and after the intervention. The study will compare changes in these outcomes within and between the intervention and control groups to evaluate the effectiveness of GEMPO e-education.

02

Conditions studied

  • Fathers' Self-Efficacy and Ability in Newborn Care

Keywords

  • GEMPO
  • Newborn care
  • Fathers
  • Self-Efficacy
  • Electronic Education
  • Newborn Care Education
03

In context

Lead sponsor

This is the only study on the registry with Musnaini Musnaini as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Male
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Fathers who have a newborn aged 0-28 days.
  2. Fathers who live in the same household as the newborn.
  3. Fathers who are involved in daily newborn care.
  4. Fathers who own a smartphone capable of accessing the GEMPO E-Education video through YouTube.
  5. Fathers who are willing to participate and provide written .

Exclusion criteria

Exclusion Criteria:

  1. Fathers who have previously participated in formal training on newborn care.
  2. Fathers or newborns whose condition prevents them from participating in all study procedures.
  3. Participants who withdraw from the study or do not complete all study procedures.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    GEMPO E-Education Group

    Participants assigned to the intervention group will receive GEMPO e-education, consisting of educational materials and an approximately -15 minute video covering newborn holding, bathing, and diaper changing techniques. The educational materials will be delivered through WhatsApp with access to the video via YouTube. Fathers' self-efficacy and ability in newborn care will be assessed before and after the intervention.

    Behavioral: GEMPO Electronic Education

  • No intervention
    Control Grup

    Participants assigned to the control group will receive routine health education according to the standard procedures of the health facilities. Fathers' self-efficacy and ability in newborn care will be assessed before and after the study period.

Interventions

  • BehavioralGEMPO Electronic Education

    GEMPO Electronic Education is an educational intervention for fathers of newborns aged 0-28 days. The intervention provides educational materials and videos on three essential newborn care skills: holding a newborn, bathing a newborn, and changing a newborn's diaper. The educational materials are delivered electronically via WhatsApp. Participants receive the educational content according to the study protocol, with evaluation conducted to assess the outcomes specified in the research protocol.

06

What researchers measure

Primary outcomes

  1. Fathers' Self-Efficacy in Newborn Care

    Self-efficacy score of fathers in performing essential newborn care, assessed using the study-specified instrument. The outcome is evaluated by comparing scores before and after the intervention.

    Time frame: Baseline before intervention and immediately after completion of the intervention.

07

Study locations

1 site
  • Puskesmas
    Pekanbaru, Riau, Indonesia
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Oct 2026; primary completion for Nov 2026, 1 month later.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 18, 2026
First posted
Oct 22, 2026
StartEst.
Oct 5, 2026
Primary completionEst.
Nov 10, 2026
CompletionEst.
Nov 10, 2026
Last update
Oct 22, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 22, 2026
Show all 1 update
  1. Oct 22, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07890077
Lead sponsor
Musnaini Musnaini
Responsible party
Musnaini Musnaini (Master's Student, Universitas Riau) — Sponsor-investigator
First posted
Oct 22, 2026
Start date
Oct 5, 2026 (estimated)
Primary completion
Nov 10, 2026 (estimated)
Completion
Nov 10, 2026 (estimated)
Last update
Oct 22, 2026

Study contacts

musnaini musnaini musnaini
Contact
musnaini0000@gmail.com
+62 82346052843 ext. +62 8234605284

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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