Effect of Multisensory (Snoezelen) Environment on Birth Outcomes
NCT ID: NCT06732544
Last Updated: 2024-12-13
Study Results
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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ACTIVE_NOT_RECRUITING
NA
23 participants
INTERVENTIONAL
2024-09-08
2025-04-30
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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experiment group
These women will spend labor in the snoezelen room.
snoezelen room
During the travail, projectors, starry ceiling visuals and blue light LEDs will be used for visual stimuli, speakers will be used as auditory stimuli, diffusers will be used for olfactory stimuli, and therapy dough will be used for touch stimuli.
control group
These women will spend the duration of labor in a standard delivery room.
routine delivery room
General practice
Interventions
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snoezelen room
During the travail, projectors, starry ceiling visuals and blue light LEDs will be used for visual stimuli, speakers will be used as auditory stimuli, diffusers will be used for olfactory stimuli, and therapy dough will be used for touch stimuli.
routine delivery room
General practice
Eligibility Criteria
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Inclusion Criteria
* Having a singleton pregnancy between 38-42 weeks of pregnancy
* Primiparous
* Labor started spontaneously
* In the latent phase of labor
* Without uterine contraction anomaly
* The leading part of the fetus is the head (in vertex position)
* No analgesia was applied
* There is no indication for cesarean section
* Amniotomy is not performed
* Fetal weight over 2500 g, fetal weight not over 4000 gr
* Pregnant women who do not have communication problems will be included in the study.
Exclusion Criteria
* Allergy, asthma, COPD, migraine, vertigo, epilepsy, etc.
* Declaring that they have a chronic disease
* Declaring that they have a psychiatric history or a diagnosed psychological disorder
* Declaring that they have a risky health condition related to pregnancy (preeclampsia, gestational DM, etc.),
* Those who report smoking, alcohol and/or substance use
* Reports that he/she has sensory sensitivity
* Declaring an allergy to lavender (Lavandula angustifolia Mill.) or lavender oil
* Declaring that there is a person with special needs in the family
* Participated in the study voluntarily and then gave up
* Pregnant women who develop any possible side effects during the study will not be included in the study.
18 Years
35 Years
FEMALE
Yes
Sponsors
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Ege University
OTHER
Amasya University
OTHER
Responsible Party
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Locations
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Amasya University Hospital
Amasya, Amasya, Turkey (Türkiye)
Countries
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Other Identifiers
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AU_Eliftez
Identifier Type: -
Identifier Source: org_study_id