- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03692923
VIRTUAL COMMUNITY for PREGNANT WOMEN
Impact of A Peer Virtual Community on Pregnant Women's Well-being: A Quasi-experimental Study
Study Overview
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
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Pregnant women were older than 20 years old
- Had at least 9 years of education.
Exclusion Criteria:
- Had complications in this pregnancy
- Had underlying medical problems with pregnancy.
Study Plan
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
Sponsor
Collaborators
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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