- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06719895
Web-Based Newborn Care Education for Primiparous Pregnant Women
December 5, 2024 updated by: Veysel Can, Yuzuncu Yıl University
For pregnant women expecting their first baby, readiness during pregnancy is an important factor in successfully performing hygienic care for their babies.
This study was planned to determine the effect of web-based education on the readiness levels of primiparous pregnant women for newborn hygienic care practices.
In this study, the aim was to support pregnant women and mothers after birth in newborn care and to develop their application skills with the web-based education program given to primiparous pregnant women.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
100
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
-
-
Tuşba
-
VAN, Tuşba, Turkey, 65000
- Recruiting
- Van Yuzuncu Yıl University
-
Contact:
- veysel can, asst. prof
- Phone Number: 05342532015
- Email: veyselcan@yyu.edu.tr
-
-
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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Aged between 15 and 19 years
- Being 19 years old and above
- Being literate
- Being primigravida
- Having a single baby (not twins or more)
- Being a volunteer to participate in the study
- Having no health problems for the mother and the baby
- Having a computer, tablet or smart phone and the ability to use it
- Having regular internet access
Exclusion Criteria:
- The mother being 18 years of age or younger
- Being multigravida and/or multiparous
- Having a health problem related to the mother or the baby
- Not having a smart phone or wireless internet during the study period
- Not filling out the survey forms incompletely and not watching videos about hygienic care of the newborn
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: Health Services Research
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: control
|
|
|
Experimental: web based education
|
experimental
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mothers' readiness levels for hygienic care of newborns
Time Frame: first test and final test 4 weeks after the first test, one month
|
Mothers' readiness levels for hygienic care of newborns
|
first test and final test 4 weeks after the first test, one month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
November 19, 2024
Primary Completion (Estimated)
January 10, 2025
Study Completion (Estimated)
January 10, 2025
Study Registration Dates
First Submitted
November 19, 2024
First Submitted That Met QC Criteria
December 5, 2024
First Posted (Estimated)
December 6, 2024
Study Record Updates
Last Update Posted (Estimated)
December 6, 2024
Last Update Submitted That Met QC Criteria
December 5, 2024
Last Verified
December 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- web based
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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