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Impact of Virtual Visit on Mothers' Attachment and Satisfaction

NCT05402787 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 62

Last updated 2022-06-02

No results posted yet for this study

Summary

Virtual visit, which is frequently used in the field of health in line with the latest technological developments, is accepted as a unique opportunity that allows babies and their families to connect in real time. Studies have reported that virtual visits increase mothers' sense of closeness to their babies and have positive effects on the attachment process (Dunham and Marin 2020; Flacking et al. 2014; Joshi et al. 2016). It is clearly emphasized that healthy and securely attached babies have positive effects on health. This study was designed as a randomized controlled experimental study in order to determine the effect of virtual visit applied to mothers whose babies are in the neonatal intensive care unit on their attachment and satisfaction.

Research Hypotheses:

H0: There is no difference between the attachment and satisfaction of mothers whose babies were hospitalized in the neonatal intensive care unit, and those who did not receive virtual visits.

H1: Attachment and satisfaction of mothers whose babies are hospitalized in the neonatal intensive care unit with virtual visits are higher than mothers who do not receive virtual visits.

Conditions

  • Virtual
  • Attachment
  • Satisfaction

Interventions

OTHER

Virtual visit

A virtual visit will be made to mothers whose babies are hospitalized in the neonatal intensive care unit

Sponsors & Collaborators

  • Sakarya University

    lead OTHER

Principal Investigators

  • Dilek Menekşe, Asist. prof. · Sakarya University

  • Öznur Tiryaki, Asist. prof. · Sakarya University

  • Nursan Çınar, Prof.Dr. · Sakarya University

  • Seda Tecik, Res.Asist. · Sakarya University

  • Hatice Solak, Nurse · Sakarya Training and Research Hospital

  • Meltem Karabay, Asist.Prof · Sakarya University

  • İbrahim Caner, Prof.Dr. · Sakarya University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-06-20
Primary Completion
2022-06-20
Completion
2023-05-01

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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 NCT05402787 on ClinicalTrials.gov