BridgeMD
New treatment option for Birth Outcomes
Official title Effect of Snoezelen Room on Birth Process
ClinicalTrials.gov ID: NCT06984614
What this study is testing
- What it's testing
- Aromatherapy, visual and auditory stimuli are used together in the Snoezelen room. Aromatherapy increases the production of endorphins, reduces the intensity of pain and distracts the attention from the pain.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 45, women only. Healthy volunteers may be eligible.
You may be able to join if
- Pregnant women who are planned to give birth vaginally in their 37th-42nd weeks of pregnancy,
- who are in their first pregnancy, who do not have any vision,
- hearing or communication problems,
- who can speak Turkish and express themselves in Turkish,
- who volunteer will be included in the study.
You likely can't join if
- Women with multiple pregnancies,
- women who are planned to give birth by cesarean section,
- women who give birth by cesarean section for any reason during the study,
- women who develop any complications during pregnancy,
- women with chronic diseases,
- women with verbal, mental, etc. communication disabilities will not be included in the study.
See the full eligibility criteria
- Pregnant women who are planned to give birth vaginally in their 37th-42nd weeks of pregnancy,
- who are in their first pregnancy, who do not have any vision,
- hearing or communication problems,
- who can speak Turkish and express themselves in Turkish,
- who volunteer will be included in the study.
- Women with multiple pregnancies,
- women who are planned to give birth by cesarean section,
- women who give birth by cesarean section for any reason during the study,
- women who develop any complications during pregnancy,
- women with chronic diseases,
- women with verbal, mental, etc. communication disabilities will not be included in the study.
- Women who have instrumental delivery (with vacuum or forceps),
- postpartum complications in the newborn, or complications related to episiotomy (such as 3rd and 4th degree laceration, hematoma) from the control or intervention groups will be excluded from the study.
The study team makes the final eligibility decision.
Where it's taking place
- Sakarya, Turkey (Türkiye)
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling female, 18 years to 45 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Sakarya, Turkey (Türkiye). Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.