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Antenatal Delivery Room Visit and Companion Support in Labor

Effects of Antenatal Delivery Room Visit and Companion Support During Labor on Maternal Comfort and Adaptation to Childbirth: A Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07407309
Enrollment
158
Registered
2026-02-12
Start date
2024-12-01
Completion date
2025-05-31
Last updated
2026-02-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Labor and Childbirth, Pregnancy

Brief summary

This study evaluated whether an antenatal visit to the delivery room combined with companion support during labor improves comfort and adaptation to childbirth among pregnant women. The childbirth environment and lack of familiarity with the delivery room may increase anxiety and reduce comfort during labor. Supportive interventions before and during labor may help women adapt more positively to the childbirth process. In this randomized controlled trial, pregnant women were assigned either to an intervention group that received an antenatal delivery room visit and continuous companion support during labor, or to a control group that received standard maternity care without these interventions. Maternal comfort and adaptation to childbirth were assessed using validated measurement tools after birth. The results of this study aim to support evidence-based maternity care practices and highlight the importance of antenatal preparation and continuous support during labor to enhance women's childbirth experiences.

Interventions

BEHAVIORALAntenatal Delivery Room Visit and Companion Support

Participants received an antenatal visit to the delivery room prior to labor and continuous companion support during the labor process, in addition to standard maternity care.

Sponsors

Nilgun Avci
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Women aged 18 years and older * Gestational age between 24 and 40 weeks * Planning a vaginal birth at the study hospital * Able to communicate in Turkish * Volunteered to participate and provided informed consent

Exclusion criteria

* High-risk pregnancy diagnosis * Planned or emergency cesarean section * Sensory or cognitive impairment

Design outcomes

Primary

MeasureTime frameDescription
Maternal Comfort During ChildbirthWithin the first 2 hours after birthMaternal comfort assessed using the Childbirth Comfort Questionnaire.

Secondary

MeasureTime frameDescription
Adaptation to Childbirth (Midwife Assessment)Within the first 2 hours after birthAdaptation to childbirth assessed by midwives using the Midwife Evaluation of Childbirth Adaptation Scale.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026