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

Gazi University

Status

Completed

Conditions

Adaptation

Pregnant Women

Postpartum Period

Mobile Applications

Treatments

Behavioral: E-Mobile Health Application

Study type

Interventional

Funder types

Other

Identifiers

NCT04783324

SultanOzkan

Details and patient eligibility

About

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.

Full 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.

Enrollment

62 patients

Sex

Female

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

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