NCT07777107

Brief Summary

This randomized controlled trial was conducted to compare the effects of focusing on warm- and cool-color visuals during labor on labor pain, state anxiety, childbirth comfort, and labor duration. Nulliparous pregnant women were randomly assigned to warm- or cool-color visual focusing groups. Visual focusing was initiated during the early stage of labor and continued throughout labor. Labor pain, state anxiety, childbirth comfort, and labor duration were assessed at predefined stages of cervical dilatation.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
64

participants targeted

Target at P50-P75 for not_applicable

Timeline
4mo left

Started Mar 2025

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress82%
Mar 2025Mar 2027

Study Start

First participant enrolled

March 1, 2025

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2026

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

August 18, 2026

Completed
2 days until next milestone

First Posted

Study publicly available on registry

August 20, 2026

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2027

Expected
Last Updated

August 20, 2026

Status Verified

August 1, 2026

Enrollment Period

1 year

First QC Date

August 18, 2026

Last Update Submit

August 18, 2026

Conditions

Keywords

Visual focusing; warm colors; cool colors; labor pain; midwifery; childbirth

Outcome Measures

Primary Outcomes (1)

  • labor pain

    Labor pain intensity was assessed using the Visual Analog Scale (VAS) at 4-5 cm, 6-7 cm, and 8-10 cm cervical dilatation. The VAS ranges from 0 to 10, with higher scores indicating greater pain intensity.

    At 4-5 cm, 6-7 cm, and 8-10 cm cervical dilatation during labor.

Secondary Outcomes (3)

  • State Anxiety

    At 6-7 cm cervical dilatation during labor.

  • Childbirth Comfort

    At 4-5 cm and 8-10 cm cervical dilatation during labor.

  • Labor Duration

    From 4 cm to 10 cm cervical dilatation during labor.

Study Arms (2)

Warm-color group

EXPERIMENTAL

A visual dominated by warm colors was placed in the delivery room, and visual focusing was initiated at 1 cm of cervical dilatation. The midwife briefly introduced the artwork and the artist and asked the women to focus their attention on the visual throughout labor, particularly during painful periods. Standard midwifery care was provided.

Other: Warm-color visual

Cool-color group

EXPERIMENTAL

A visual dominated by cool colors was placed in the delivery room, and visual focusing was initiated at 1 cm of cervical dilatation. The midwife briefly introduced the artwork and the artist and asked the women to focus their attention on the visual throughout labor, particularly during painful periods. Standard midwifery care was provided.

Other: Cool-color visual

Interventions

A visual dominated by warm colors was placed in the delivery room, and visual focusing was initiated at 1 cm of cervical dilatation. The midwife briefly introduced the artwork and the artist and asked the women to focus their attention on the visual throughout labor, particularly during painful periods.

Warm-color group

A visual dominated by cool colors was placed in the delivery room, and visual focusing was initiated at 1 cm of cervical dilatation. The midwife briefly introduced the artwork and the artist and asked the women to focus their attention on the visual throughout labor, particularly during painful periods.

Cool-color group

Eligibility Criteria

Age18 Years+
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsOnly pregnant women were eligible to participate in the study.
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Nulliparous pregnant women Singleton pregnancy Term pregnancy (37-42 weeks of gestation) Cephalic fetal presentation Spontaneous onset of labor Cervical dilatation of 1 cm at enrollment Ability to communicate in Turkish Voluntary participation in the study -

You may not qualify if:

  • High-risk pregnancy or obstetric complications Presence of a condition requiring emergency obstetric intervention Use of pharmacological analgesia during labor Visual impairment that could interfere with focusing on the visual Development of maternal or fetal complications requiring discontinuation of the intervention

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Balıkesir University

Balıkesir, 6100, Turkey (Türkiye)

Location

Related Publications (2)

  • Turkmen H, Cetinkaya S, Kilic H, Tuna SD, Sirvanci M, Mutlu H. The Effect of Ice Massage Applied to the SP6 Point on Labor Pain, Labor Comfort, Labor Duration, and Anxiety: A Randomized Clinical Trial. J Midwifery Womens Health. 2024 Jul-Aug;69(4):491-498. doi: 10.1111/jmwh.13600. Epub 2024 Jan 15.

    PMID: 38223923BACKGROUND
  • Turkmen H, Cetinkaya S, Kilic H, Apay E, Karamuftuoglu D, Yoruk S, Ozkirim E. Effect of Focusing on Maryam's Flower During the First Stage of the Labor on the Labor Pain, Labor Duration, and Levels of Comfort and Satisfaction. Clin Nurs Res. 2021 Jul;30(6):780-789. doi: 10.1177/1054773820984911. Epub 2020 Dec 29.

    PMID: 33371726BACKGROUND

MeSH Terms

Conditions

Labor PainAnxiety Disorders

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsMental Disorders

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
associate professor

Study Record Dates

First Submitted

August 18, 2026

First Posted

August 20, 2026

Study Start

March 1, 2025

Primary Completion

March 1, 2026

Study Completion (Estimated)

March 1, 2027

Last Updated

August 20, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

Locations