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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04783324
Enrollment
62
Registered
2021-03-05
Start date
2021-03-25
Completion date
2021-08-29
Last updated
2021-11-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adaptation, Mobile Applications, Postpartum Period, Pregnant Women

Keywords

Mobile Applications, Postpartum Period, Adaptation, Randomized Controlled Trial

Brief 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.

Detailed 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.

Interventions

BEHAVIORALE-Mobile Health Application

The e-mobile health application prepared by the researcher will be used. E-mobile health application include information about postpartum care.

Sponsors

Gazi University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Intervention model description

The study consists of two groups: Experimental group and control group.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Postpartum AdaptationAt postpartum tenth day (baseline) and last-interview at postpartum sixth week (change from baseline at sixth week)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.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026