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Clinical Trials/NCT01687933
NCT01687933CompletedPhase 2

Principal Investigator

Mashhad University of Medical Sciences0 sites30 target enrollmentStarted: February 2011Last updated:
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Conditions

Trial Snapshot

Phase
Phase 2
Status
Completed
Enrollment
30
Primary Endpoint
pain and anxiety
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

There are different medicinal and non medicinal methods to control labor pain. Today, much attention has been on non medicinal methods because of limitations and complications of medical procedures. Virtual reality is a new and promising method of diversion of mind that may have an impact on labor pain. This study was conducted to determine the effect of virtual reality on the first stage of labor pain.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 29 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •low risk pregnancy
  • •primipara

Exclusion Criteria

  • •vision or ear disorders
  • •History of motion sickness or headaches
  • •psychological disease or Addiction

Outcomes

Primary Outcomes

pain and anxiety

Time Frame: up to 8 months

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Samira Ebrahimzadeh Zagami

MUMS

Mashhad University of Medical Sciences

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