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Development of Postnatal Mobile Support Application

NCT03415321 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 124

Last updated 2020-06-23

No results posted yet for this study

Summary

A mobile support application will be developed that will support mothers in the postpartum period and will be tested the effects of application on anxiety and depression symptoms.The study will consist of two phases. The first phase of the action research (participant design method) method will be done to provide postpartum mobile support application. In the second stage, postpartum mobile support application will be evaluated for the anxiety and depression symptoms of the mothers after six weeks of use.

Conditions

Interventions

DEVICE

Postpartum Mobile Support Application

Women in the experimental group will use the Postpartum Mobile Support Application during six weeks after birth. Women will be evaluated three times in total, one for the first day after birth, second for the seventh day after birth and the last for the sixth week after birth. Short messages and calls will be remind of women's Postpartum Mobile Support Application use

Sponsors & Collaborators

  • Necmettin Erbakan University

    lead OTHER

Principal Investigators

  • Vesile KOÇAK · Researcher

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
55 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-04-04
Primary Completion
2019-07-30
Completion
2020-02-20

Countries

  • Turkey (Türkiye)

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03415321 on ClinicalTrials.gov