The Effect of Exposure to an Informative Video on Maternal Anxiety

NCT ID: NCT04136301

Last Updated: 2019-10-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

152 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-11-01

Study Completion Date

2020-08-30

Brief Summary

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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.

Detailed Description

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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

Conditions

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Anxiety Labor Pain Patient Satisfaction

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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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

Group Type EXPERIMENTAL

Informative Video group

Intervention Type OTHER

Informative Video group before labor in nulliparous women

control arm

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

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Informative Video group

Informative Video group before labor in nulliparous women

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

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

Exclusion Criteria

Refuse to participate Contraindications for vaginal delivery
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Wolfson Medical Center

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Wolfson medical center

Holon, , Israel

Site Status RECRUITING

Countries

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Israel

Facility Contacts

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Hadas Miremberg, MD

Role: primary

972526741740

Other Identifiers

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0093-19-WOMC

Identifier Type: -

Identifier Source: org_study_id

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