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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05492981
Other study ID # 2020/01123
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date July 5, 2021
Est. completion date July 30, 2022

Study information

Verified date July 2022
Source National University Hospital, Singapore
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Informed decision-making regarding aneuploidy screening has been reported to be low. Poor knowledge and the lack of deliberation have been cited as reasons for uninformed choices, highlighting the need for adequate pre-test counselling. We conducted a study to assess if an educational video improves informed choice in a clinical setting where both the combined first trimester screen and non-invasive prenatal screening are offered routinely to pregnant women.


Description:

Women attending the antenatal clinic with a viable singleton pregnancy below 14 weeks were randomized to receive routine counselling by their obstetrician or the intervention, where they watched a 16-minute educational video on aneuploidy screening before their consult. The primary outcome, rate of informed choice, was assessed using an adapted multidimensional measure of informed choice (MMIC) questionnaire, where informed choice was defined as good knowledge and value-consistent behaviour. Secondary outcomes included informed choice with deliberation, decisional conflict and anxiety.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 286
Est. completion date July 30, 2022
Est. primary completion date February 24, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 21 Years to 50 Years
Eligibility Inclusion Criteria: - aged 21 years or older - English speaking - had a viable singleton pregnancy below 14 weeks gestation Exclusion Criteria: - women who had any prior discussion with a clinician regarding aneuploidy screening for their current pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Enhanced (intervention) education
See arm description

Locations

Country Name City State
Singapore National University Hospital Singapore

Sponsors (1)

Lead Sponsor Collaborator
National University Hospital, Singapore

Country where clinical trial is conducted

Singapore, 

Outcome

Type Measure Description Time frame Safety issue
Primary Informed choice Outcome will be measured using the modified multidimensional measure of informed choice (MMIC). Day 0
Secondary Deliberation Outcome will be measured using 6 questions to measure deliberation on a five-point Likert scale Day 0
Secondary Knowledge Outcome will be measured using a 19-item validated true/false knowledge questionnaire. Day 0
Secondary Value-consistent behaviour Attitudes towards testing options were assessed using a validated questionnaire and deemed to be value consistent if a participants had a positive attitude towards the test option that they chose, or a negative attitude towards all test options and chose not to test. Day 0
Secondary anxiety Anxiety was assessed using the Spielberger State trait anxiety inventory (STAI-6) short form which consisted of 6 items Day 0
Secondary Decisional Conflict Decisional conflict was measured using a validated Decisional Conflict Scale (DCS) Day 0
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