CClinicalTrials.gg
Status unknownNCT04136301Updated Oct 23, 2019

The Effect of Exposure to an Informative Video on Maternal Anxiety

An interventional study of Informative Video group in Anxiety, Labor Pain and Patient Satisfaction, sponsored by Wolfson Medical Center. Status unknown at 1 site in Israel. Open to female participants aged 18 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-10-23.

Sponsored by Wolfson Medical Center · Not applicable, Interventional, and Supportive care

The sponsor has not verified this record recently (last verified Oct 2019), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
152
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
Female
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Study summary

Stress and anxiety during childbirth have negative consequence on both mother and fetus. Previous studies have learned the effect of several intervention to reduce anxiety during labor- such as music and foot reflexology. Nevertheless, data for informative video before labor for reducing stress and anxiety are sparse. The present study aimed to review and determine the effect of informative video on anxiety, pain and outcomes of the labor in primigravida women.

Read the detailed description

A randomized control trial studying the effect of exposure to an informative video regarding labor and possible obstetrics emergencies on maternal anxiety and postpartum satisfaction

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Conditions studied

  • Anxiety
  • Labor Pain
  • Patient Satisfaction
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In context

Labor Pain

396 studies on the registry are indexed under Labor Pain; 66 are open to participants now.

This study's planned enrollment of 152 is above the median of 100 across 326 interventional studies indexed under Labor Pain.

Browse Labor Pain studies →

Lead sponsor

Wolfson Medical Center is the lead sponsor of 113 studies on the registry; 16 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

above 18 years of age Nulliparus women Informed consent Reads and understand Hebrew >37 weeks of gestation

Exclusion criteria

Exclusion Criteria:

Refuse to participate Contraindications for vaginal delivery

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Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
152 participants (estimated)

Study arms

  • Experimental
    Informative video arm

    Nuliparus women admitted to an induction will be exposed to informative video with data regarding labor and possible obstetric emergencies such as cesarean delivery. All patients will answer the State-Trait Anxiety Inventory (STAI) before and after intervention

    Other: Informative Video group

  • No intervention
    control arm

    no intervention. All patients will answer the State-Trait Anxiety Inventory (STAI) before and after delivery.

Interventions

  • OtherInformative Video group

    Informative Video group before labor in nulliparous women

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What researchers measure

Primary outcomes

  1. The State-Trait Anxiety Inventory score in delivery room

    STAI questionnaire before and after delivery room

    Time frame: 1 hour

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Study locations

1 of 1 sites recruiting
  • Wolfson medical center
    Holon, Israel
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 23, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04136301
Lead sponsor
Wolfson Medical Center
Responsible party
Sponsor
First posted
Oct 23, 2019
Start date
Nov 1, 2019 (estimated)
Primary completion
Aug 1, 2020 (estimated)
Completion
Aug 30, 2020 (estimated)
Last update
Oct 23, 2019

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2019. You cannot join it, but the record below documents what was studied.

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