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Clinical Trials in Turkey / NCT07248787
Starting soon Not applicable

Effect of Multi-Sensory Interventions on Labor Pain, Comfort, and Birth Satisfaction

NCT07248787 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-12-01
Last updated
2025-11-25

Condition(s) studied

Labor PainBirth Satisfaction

Investigational drug(s) / intervention(s)

Sacral MassageLavender AromatherapyTurkish Makam MusicAquarium Visual Stimulus

Sacral Massage: A 10-minute sacral massage applied by a trained midwife during each stage of labor (three sessions in total). The massage involves circular hand motions to relieve pain and promote relaxation.

Lavender Aromatherapy: Lavender essential oil diffused for 20 minutes during each stage of labor (three times total) to promote calmness and reduce pain intensity.

Turkish Makam Music: Rehavi and Nihavend Turkish makam music (45-65 dB) played through headphones for 20 minutes during each stage of labor (three times total).

Aquarium Visual Stimulus: Continuous presentation of an aquarium scene video during the active phase of labor to provide visual distraction and relaxation.

Study summary

The goal of this clinical trial is to learn whether different multi-sensory methods can help lower labor pain and improve comfort and birth satisfaction among pregnant women giving birth vaginally.

The main questions this study aims to answer are:

Do supportive methods such as massage, lavender aromatherapy, Turkish makam music, or aquarium visual stimulation help women feel less labor pain compared to standard care?

Do these methods increase women's comfort and satisfaction during labor?

Participants will be randomly assigned to one of five groups:

Sacral massage group - will receive 10-minute sacral massages three times during labor.

Lavender aromatherapy group - will inhale lavender essential oil through a diffuser for 20 minutes, three times during labor.

Music therapy group - will listen to Turkish makam music (Rehavi or Nihavend) for 20 minutes, three times during labor.

Visual stimulation group - will watch a live aquarium image continuously during active labor.

Control group - will receive standard maternity care only.

All participants will give informed consent and receive care in the obstetrics unit of Kütahya City Hospital, Türkiye.

Researchers will measure:

Labor pain intensity at 4-5 cm, 6-7 cm, and 8-10 cm cervical dilatation using a Visual Analogue Scale (VAS).

Comfort level at 8-9 cm using the Comfort Characteristics Questionnaire (CCQ).

Birth satisfaction about 2 hours after delivery using the Birth Satisfaction Scale (BSS).

Labor duration will also be recorded.

This study will help determine which sensory methods are most effective and comfortable for pregnant women, and may guide supportive care practices during childbirth.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
40 Years
Healthy volunteers
No
Inclusion Criteria: * Pregnant women aged 18 to 40 years * Gestational age ≥ 37 weeks (term pregnancy) * Singleton pregnancy with cephalic presentation * Expected vaginal delivery * Cervical dilation of at least 3 cm at hospital admission * Able to communicate in Turkish and provide informed consent Exclusion Criteria: * Diagnosed high-risk pregnancy (e.g., preeclampsia, placenta previa, fetal distress) * History of cesarean section or uterine surgery * Use of epidural, spinal anesthesia, or opioid analgesics during labor * Visual, auditory, or olfactory impairments that may affect perception of the interventions * Allergy or sensitivity to lavender oil * Emergency cesarean section or any complication requiring medical intervention * Refusal or withdrawal of consent at any stage

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Kütahya City Hospital Kütahya Turkey (Türkiye)

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07248787 on ClinicalTrials.gov ↗ ← All trials in Turkey