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The Effect of Exposure to Informative Video Before Cesarean Delivery on Maternal Anxiety

W

Wolfson Medical Center (WMC)

Status

Completed

Conditions

Maternal Distress (During Labor)
Anxiety

Treatments

Behavioral: Informative video

Study type

Interventional

Funder types

Other

Identifiers

NCT04176107
0092-19-WOMC

Details and patient eligibility

About

The incidence of cesarean deliveries (CD) worldwide is increasing, around 30% in United States. Although very common surgery women undergoing non emergent CD still experience fear and anxiety. It is known that increased levels of stress can negatively affect pain perception and the usage of analgesics postoperatively as well as lactation.

this present study investigate the effect of exposure to informative video before cesarean delivery on maternal anxiety.

Full description

A multi-center randomized control trial the will examine the effect of exposure to informative video before cesarean delivery on maternal anxiety and satisfaction

Enrollment

126 patients

Sex

Female

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Hebrew speaking
  • Informed consent
  • First cesarean delivery
  • Non emergent elective CD

Exclusion criteria

  • Non Hebrew speaking
  • Refuse to participate
  • Emergency CD

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

126 participants in 2 patient groups

Study group- video+questionnaire
Other group
Description:
The study group will be exposed to a video at admission to an elective cesarean delivery. The video will have information regarding the admission, pre-operation preparation and post- operation recovery. All patients will answer a questionnaire at admission, before surgery and 24 hours later. the questionnaires will evaluate the impact of exposure to informative video before caesarean delivery on anxiety and stress measured by State-Trait Anxiety Inventory (STAI).
Treatment:
Behavioral: Informative video
Control group- questionnaire only
No Intervention group
Description:
All patients will answer a questionnaire at admission, before surgery and 24 hours later. the questionnaires will evaluate anxiety and stress measured by State-Trait Anxiety Inventory (STAI) without intervention.

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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