VIRTUAL COMMUNITY for PREGNANT WOMEN

October 2, 2018 updated by: WAN-RU WU, Tzu Chi University

Impact of A Peer Virtual Community on Pregnant Women's Well-being: A Quasi-experimental Study

The study aimed to investigate the effect of exclusive peer-to-peer virtual support on pregnant women's well-being including physical symptoms, depression, social support, maternal attachment, and pregnancy adaptation.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

The pregnancy period is marked by not only the joy and excitement of bonding with her baby but also dramatic changes in her body. The Internet's convenience and anonymity provide great possibilities for pregnant women to create a social network for sharing personal stories, seeking information and asking questions, and expressing own emotions and concerns.

Although health-related online communities are emerging rapidly around the globe, little is known about the impact of a virtual peer community on pregnant women's well-being.

The study enrolled 138 pregnant women, who were assigned to either the experimental or control groups. After obtaining informed consent from participants, we asked them to fill out the baseline questionnaires (Time 1). The first and second follow-ups (Times 2 and 3) were conducted at 22-24 and 36-38 weeks of pregnancy, respectively. Participants in the experimental group received ordinary prenatal care in addition to virtual community participation, and those in the control group received only ordinary prenatal care.

Study Type

Interventional

Enrollment (Actual)

138

Phase

  • Not Applicable

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  1. Pregnant women were older than 20 years old
  2. Had at least 9 years of education.

Exclusion Criteria:

  1. Had complications in this pregnancy
  2. Had underlying medical problems with pregnancy.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: control group
participants received ordinary prenatal care.
Experimental: virtual community group
participants were invited to join a virtual community to interact with peers in addition to their ordinary prenatal care.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The pregnancy adaptation scale
Time Frame: repeated measured at second trimester (22-24 weeks of pregnancy), and the third trimester (36-38 weeks of pregnancy).
Used to investigate the changes in the scores of pregnancy adaptation. Items are scored from 0 to 3 and they are summed to compute a total score ranging from 0 to 84. Higher scores indicate better pregnancy adaptation.
repeated measured at second trimester (22-24 weeks of pregnancy), and the third trimester (36-38 weeks of pregnancy).
The Edinburgh Depression Scale
Time Frame: repeated measured at second trimester (22-24 weeks of pregnancy), and the third trimester (36-38 weeks of pregnancy).
Used to investigate the changes in the scores of depression. Items are scored from 0 to 3 and they are summed to compute a total score ranging from 0 to 30. The cut-off point for depression is a total score of 12 or above.
repeated measured at second trimester (22-24 weeks of pregnancy), and the third trimester (36-38 weeks of pregnancy).

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Symptoms Checklist
Time Frame: repeated measured at second trimester (22-24 weeks of pregnancy), and the third trimester (36-38 weeks of pregnancy).
Used to investigate the changes in the scores of pregnancy-related physical symptoms. Items are scored from 1 to 4 and they are summed to compute a total score ranging from 22 to 88. Higher scores indicate experiencing more symptoms.
repeated measured at second trimester (22-24 weeks of pregnancy), and the third trimester (36-38 weeks of pregnancy).
The Social Support Scale
Time Frame: repeated measured at second trimester (22-24 weeks of pregnancy), and the third trimester (36-38 weeks of pregnancy).
Used to investigate the changes in the scores of social support perception. Items are scored from 1 to 5 and they are summed to compute a total score ranging from 20 to 100. higher scores indicate perceived higher social support from family, peer pregnant women, friends, and healthcare providers.
repeated measured at second trimester (22-24 weeks of pregnancy), and the third trimester (36-38 weeks of pregnancy).
The Maternal-Fetal Attachment Assessment Scale
Time Frame: repeated measured at second trimester (22-24 weeks of pregnancy), and the third trimester (36-38 weeks of pregnancy).
Used to investigate the changes in the scores of maternal-fetal attachment. Items are scored from 1 to 5 and they are summed to compute a total score ranging from 39 to 195. Higher scores indicate higher maternal-fetal attachment.
repeated measured at second trimester (22-24 weeks of pregnancy), and the third trimester (36-38 weeks of pregnancy).

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 1, 2012

Primary Completion (Actual)

January 31, 2015

Study Completion (Actual)

January 31, 2015

Study Registration Dates

First Submitted

September 21, 2018

First Submitted That Met QC Criteria

September 30, 2018

First Posted (Actual)

October 2, 2018

Study Record Updates

Last Update Posted (Actual)

October 4, 2018

Last Update Submitted That Met QC Criteria

October 2, 2018

Last Verified

October 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • TCU

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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