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The Effect of Exposure to an Informative Video About Amniocentesis Before the Procedure on Maternal Anxiety

The Effect of Exposure to an Informative Video About Amniocentesis Before the Procedure on Maternal Anxiety

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05463549
Enrollment
100
Registered
2022-07-19
Start date
2022-02-08
Completion date
2022-12-30
Last updated
2023-03-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Amniocentesis Affecting Fetus or Newborn, Anxiety in Pregnancy, Pregnancy Related

Keywords

explanatory video, anxiety reduction, amniocentesis, pregnancy

Brief summary

The effect of exposure to an informative video about amniocentesis before the procedure on maternal anxiety

Detailed description

Amniocentesis is a common sonography-guided procedure that is usually preformed during the second trimester of pregnancy in order to obtain neonatal genetic information. Previous studies have shown that although the risk of a major complication is small, many women experience profound anxiety regarding the procedure. Many stress-relieving techniques have been proposed and studied concerning stress-related interventions during pregnancy. However, the use of an informative video that is a simple, accessible, widely accepted tool has not been tested in the context of amniocentesis. In this interventional study the investigators aim to examine the effect of an informative pre-procedural video on anxiety and pain levels in women undergoing amniocentesis.

Interventions

An informative instructional film regarding the amniocentesis procedure including answers to frequently asked questions.

Sponsors

Wolfson Medical Center
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

Data regarding maternal characteristics, anxiety and pain levels as reported by the patients via the questioners will be stored according to random serial numbers without intervention type. The investigator handling the statistical analysis will be unaware of the patient's exposure.

Intervention model description

Women assigned to undergo amniocentesis during the trail time-period will be invited to participate in the study and will be signed a consent form.The randomization will be based on different days for each intervention - a day specified to women comprising of the research group while the following clinic day will be dedicated to women from the control group. The study group will watch an informative video while waiting for amniocentesis, and the control group will not watch the video while waiting.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Women who come for amniocentesis in the Edith Wolfson Medical Center * Women who sign a consent form to enroll to the study.

Exclusion criteria

* Women under 18 years of age. * Women who do not speak Hebrew

Design outcomes

Primary

MeasureTime frameDescription
Assessment of change in anxiety levels between before and after undergoing the amniocentesisEach patient will answer the STAI questionnaire twice - within 2 hours before the operation and watching the video (S1) and within 30 minutes after performing amniocentesis (S2) to assess the change in anxiety levels before and after the operationWomen recruited to the study will answer the Spielberger's state-trait anxiety inventory questionnaire- a validated questionnaire for assessing anxiety which includes 20 statements expressing different states of anxiety. The patients will be asked to rate to what extent they currently relate to the statement written on a scale of 1 to 4 (1- does not agree at all and 4- strongly agrees). The final score in each questionnaire is obtained by summing the scores of each statement, while the scores of positive statements reflecting anxiety-free behavior will be reversely summed. Higher scores indicate higher level of anxiety.

Secondary

MeasureTime frameDescription
Intensity of pain, discomfort, satisfaction with the video and satisfaction in generalThe questionnaire will be filled within 30 minutes after performing amniocentesisThese parameters will be measured using the item visual analog scales 11 questionnaire containing questions reflecting pain, discomfort and satisfaction levels. Each statement scores between 0-10 as a reflection of the patients' identification with the statement- each statement reflecting different aspects of the patients' experience: question 1- pain during the procedure question 2- pain 10 minutes after the procedure question 3- general unpleasantness question 4- anxiety during procedure question 5- satisfaction with information about procedure question 6- overall satisfaction with treatment question 7- level of discomfort as a result of informative video prior to the amniocentesis question 8- level of anxiety caused by watching the informative video question 9-importance of informative video for understanding the amniocentesis procedure

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026