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

NCT ID: NCT04783324

Last Updated: 2021-11-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

62 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-03-25

Study Completion Date

2021-08-29

Brief Summary

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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

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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.

Conditions

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Postpartum Period Pregnant Women Adaptation Mobile Applications

Keywords

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Mobile Applications Postpartum Period Adaptation Randomized Controlled Trial

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

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

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Experimental Group

Pregnant women in the intervention group will use the e-mobile health application developed by the researcher.

Group Type EXPERIMENTAL

E-Mobile Health Application

Intervention Type BEHAVIORAL

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

Control Group

Pregnant women in the control group will not be intervened and standard care will be applied.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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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.

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Gazi University

OTHER

Sponsor Role lead

Responsible Party

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Sultan Ozkan

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Şengül Yaman Sözbir, PhD

Role: PRINCIPAL_INVESTIGATOR

Gazi University

Locations

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Ankara Koru Hospital

Ankara, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

References

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Ozkan Sat S, Yaman Sozbir S. Randomized Controlled Trial of a Mobile Health Application Based on Roy's Adaptation Model on Postpartum Adaptation. Nurs Res. 2023 May-Jun 01;72(3):E16-E24. doi: 10.1097/NNR.0000000000000647. Epub 2023 Feb 21.

Reference Type DERIVED
PMID: 36920158 (View on PubMed)

Other Identifiers

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SultanOzkan

Identifier Type: -

Identifier Source: org_study_id