The Effect of the E-Mobile Health Application on Postpartum Adaptation

Pregnant Women Clinical Trial

Official title:

The Effect of the E-Mobile Health Application for Pregnant Women Created Based on the Roy's Adaptation Model on Postpartum Adaptation

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04783324
• Other study ID #: SultanOzkan
• Status: Completed
• Phase: N/A
• Start date: March 25, 2021
• Est. completion date: August 29, 2021

Study information

• Verified date: October 2021
• Source: Gazi University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this research is to determine the effect of the e-mobile health application on postpartum adaptation. The study will consist of two groups: Experimental group and control group.

Description:

This is a randomized controlled trial. A questionnaire and The Postpartum Self-Evaluation Questionnaire will be used to collect data. The main hypothesis of the research: Postpartum Self-Evaluation Questionnaire total mean score of women who use e-mobile health application created according to Roy's Adaptation Model is not different from the total mean score of women in the control group.

Research sample will consist of a total of 62 pregnant women, 31 in the experimental group and 31 in the control group. The data will be evaluated with the SPSS (Statistical Package of SocialSciences) 24.0 package program.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 62
• Est. completion date: August 29, 2021
• Est. primary completion date: August 29, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 35 Years

Eligibility

Inclusion Criteria:

• Primiparous

• Being in the 32nd week of pregnancy and above

• Not getting any diagnosis that poses a risk for pregnancy (Multiple pregnancy, Gestational Diabetes, Preeclampsia, Eclampsia, Placenta Previa, Fetal Anomaly, Intrauterine Growth Retardation)

• Speaking Turkish

• To be at least a primary school graduate

• Having a smart phone with Android operating system

Exclusion Criteria:

• Multiparous

• Being under 32 weeks of pregnancy

• Getting any diagnosis that poses a risk to pregnancy (Multiple pregnancy, Gestational Diabetes, Preeclampsia, Eclampsia, Placenta Previa, Fetal Anomaly, Intrauterine Growth Retardation)

• Not speaking Turkish

• Having a smartphone with an operating system other than Android

Related Conditions & MeSH terms

• Adaptation
• Mobile Applications
• Postpartum Period
• Pregnant Women

Intervention

Behavioral:
• E-Mobile Health Application
The e-mobile health application prepared by the researcher will be used. E-mobile health application include information about postpartum care.

Locations

Country	Name	City	State
Turkey	Ankara Koru Hospital	Ankara

Sponsors (1)

Lead Sponsor	Collaborator
Gazi University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Postpartum Adaptation	Postpartum adaptation according to Postpartum Self Evaluation Scale. Postpartum self evaluation questionnaire consists of 82 questions in total. The questions are scored between 1 and 4 points. The minimum value that can be obtained from the scale is 82, the maximum value is 328. It is seen that the lower the score in this scale, the higher the postpartum adaptaion of the individual.	At postpartum tenth day (baseline) and last-interview at postpartum sixth week (change from baseline at sixth week)