Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
FEMALE
Healthy Volunteers
ID06984614

Effect of Snoezelen Room on Birth Process: a Randomized Controlled Study

Led by Sakarya University · Updated on 2025-05-22

104

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

Sponsors

S

Sakarya University

Lead Sponsor

H

Health Institutes of Turkey

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to evaluate the effect of using a Snoezelen room during the delivery process for first-time pregnant women. The Snoezelen room combines aromatherapy with visual and auditory stimuli to help reduce pain by increasing endorphin production and distracting attention from pain. Although this approach is growing in popularity internationally, it is being introduced for the first time in delivery services within this country, with the study conducted at a hospital equipped for gynecology and obstetrics. Participants are randomly assigned to two groups: one delivers in a specially designed Snoezelen room, and the other in a standard delivery room following routine care. During labor, the women in the Snoezelen room will experience sensory stimulation intended to promote relaxation and comfort. Pain levels will be monitored hourly using a Visual Analog Scale (VAS), and additional assessments like the Fear of Childbirth Scale and Birth Comfort Scale will be conducted at specific stages of cervical dilation. Blood samples will be taken three times to measure beta-endorphin levels. The control group will undergo the same assessments and blood sampling but deliver under standard care. Throughout the study, researchers will collect data using various forms and scales before, during, and after delivery, including birth satisfaction assessed two hours postpartum. Pain, comfort, fear, and biochemical markers will be carefully monitored to understand the Snoezelen room's impact on the birth process. The study is planned to run from October 2023 to July 2024, with detailed observation and data recording to compare outcomes between the two groups.

CONDITIONS

Brief Title

Effect of Snoezelen Room on Birth Process

Who Can Participate

Age: 18Years - 45Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnant women planning vaginal birth between 37 and 42 weeks of pregnancy
  • First pregnancy (primiparous women)
  • No vision, hearing, or communication problems
  • Able to speak and express themselves in Turkish
  • Volunteers willing to participate in the study
Not Eligible

You will not qualify if you...

  • Women with multiple pregnancies
  • Women planned for cesarean section or who have cesarean delivery during the study
  • Women who develop complications during pregnancy
  • Women with chronic diseases
  • Women with verbal, mental, or communication disabilities
  • Women who have instrumental delivery (vacuum or forceps)
  • Newborns with postpartum complications or mothers with episiotomy-related complications (such as severe lacerations or hematoma) will be excluded from the study from both groups

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - Duration of labor until birth

Participants in the intervention group complete their labor in a specially designed Snoezelen room to promote comfort and relaxation. Participants in the control group complete labor in a standard delivery room with routine care. Pain levels are assessed hourly during labor, and various scales related to fear, comfort, and satisfaction are applied at specific cervical dilation stages and after birth. Blood samples are taken three times to measure beta-endorphin levels.

1 labor and delivery visit with hourly assessments during labor and a follow-up assessment 2 hours after birth

Trial Site Locations

Total: 1 location

1

Sakarya Training and Research Hospital, Maternity Campus

Sakarya, Turkey (Türkiye)

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Research Team

M

Melek Balçık Çolak, RM, PhD, Asst. Prof.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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