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NCT04966312

Preoperative Educational Videos Reduce Maternal Anxiety Whose Children Received Congenital Heart Disease Surgery

Completed NA Last updated 19 July 2021
What this trial tests

NA trial testing Preoperative educational videos plus routine education in Educational Videos in 120 participants. Completed in 31 December 2019.

Timeline
1 January 2017
Primary endpoint
31 December 2019
31 December 2019

Quick facts

Lead sponsorChung Shan Medical University Hospital
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposeother
Enrollment120
Start date1 January 2017
Primary completion31 December 2019
Estimated completion31 December 2019
Sites1 location across Taiwan

Drugs / interventions tested

Conditions studied

Sponsor

Chung Shan Medical University Hospital

Who can join

Adults 23 to 48, female only, with Educational Videos or Maternal Anxiety. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of Preoperative educational videos plus routine education

Trials testing the same drug.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04966312.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing