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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04966312
Other study ID # CS13143
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2017
Est. completion date December 31, 2019

Study information

Verified date July 2021
Source Chung Shan Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To examine if educational digital video disk can reduce maternal anxiety and depression if their children undergo congenital heart disease surgery and when surgical or post-surgical complications occur. Compared to only routine education, adding digital video disk could decrease mothers' anxiety more after education, and until the day of discharge. Compared to only routine education, adding digital video disk could decrease mothers' anxiety more on the discharge day if their child had surgical or post-surgical complications.


Description:

Aims and objectives: To examine if educational digital video disk can reduce maternal anxiety and depression if their children undergo congenital heart disease surgery and when surgical or post-surgical complications occur. Background: Mothers experience anxiety and depression if their children undergo conditions mentioned above. Design: A randomized control-group pretest-posttest design. The CONSORT checklist is used. Methods: In a teaching hospital, 120 mothers whose children underwent first elective surgery for congenital heart disease were randomly divided into group 1: 60 mothers receiving routine education plus digital video disk before surgery; and group 2: 60 mothers receiving routine education. Between groups, mothers' anxiety and depression levels were compared (1) before education, (2) after education (before surgery) and (3) on the discharge day. Among mothers whose children had surgical or post-surgical complications, the effect of watching the digital video disk on anxiety and depression at discharge day was evaluated.


Recruitment information / eligibility

Status Completed
Enrollment 120
Est. completion date December 31, 2019
Est. primary completion date December 31, 2019
Accepts healthy volunteers No
Gender Female
Age group 23 Years to 48 Years
Eligibility Inclusion Criteria: - Mothers, whose children underwent first elective cardiac surgery for congenital heart disease - Mothers should have been the primary caregivers - Mothers able to communicate effectively, either orally or in writing Exclusion Criteria: - Mothers of children with genetic disorders - Mothers of children with non-cardiac congenital anomalies - Mothers of children with diseases such as cerebral palsy, epilepsy, psychiatric diseases, and * * Mothers of children with chronic lung diseases

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Preoperative educational videos plus routine education
Mothers receiving routine education plus digital video disk before their children receiving congenital heart disease surgery. The content was the same as the routine education but was presented audio-visually, and the video was easy to understand by the general public.
Preoperative routine education
Mothers receiving routine education before their children receiving congenital heart disease surgery

Locations

Country Name City State
Taiwan Chung Shan Medical University Hospital Taichung

Sponsors (1)

Lead Sponsor Collaborator
Chung Shan Medical University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary The change of Mother's anxiety The number scores of mother's anxiety between "routine education" and "routine plus DVD education" groups.
Beck Anxiety Inventory (BAI) was used to evaluate the number scores of anxiety.
day 1 (baseline, before education), day 1 (after education), day 5-7 (discharge day)
Primary The change of Mother's depression The number scores of mother's depression between "routine education" and "routine plus DVD education" groups.
Beck Depression Inventory (BDI) was used to evaluate the number scores of depression.
day 1 (baseline, before education), day 1 (after education), day 5-7 (discharge day)
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