Effect of Light Color Temperature Applied During Breastfeeding on Mother's Stress, Anxiety, Peace and Breastfeeding Motivation

Effect of Light Color Temperature Applied During Breastfeeding on Mother's Stress, Anxiety, Peace and Breastfeeding Motivation: A Randomized Controlled Trial

Breastfeeding is an important condition for the health of the mother and the baby, which is the most difficult for mothers after birth. Since it is an important practice for both the mother and the baby, the evaluation and reduction of the mother's stress factors can help the hospital to regulate the lighting of the breastfeeding room. In addition, setting the light color temperature to a more appropriate kelvin can make a positive contribution to the hospital in terms of costs. For this purpose, when researchers look at the literature, we have not come across a randomized controlled study examining the effect of the light color temperature applied during breastfeeding on the mother's stress, anxiety, peace and breastfeeding motivation. Researchers' purpose is to determine the effect of the light color temperature applied during breastfeeding on the mother's stress, anxiety, peace and breastfeeding motivation.

Study Overview

• Status: Not yet recruiting
• Conditions: Stress; Anxiety; Light
• Intervention / Treatment: Other: Light application

• Study Type: Interventional
• Enrollment (Estimated): 100
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Emine Yıldırım, Assistant Professor; Phone Number: 05066268672; Email: eminekucukyildirim@gmail.com
• Study Contact Backup: Name: Emine Yıldırım; Phone Number: 05066268672; Email: emineyildirim@osmaniye.edu.tr

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Child
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

• Mothers who have given birth for the first time,
• being 18 years of age and older,
• volunteering.

Exclusion Criteria:

• Being a mother who has given birth to more than one child,
• having any problem that prevents communication (such as not knowing Turkish, having hearing, speaking and understanding disorders),
• receiving psychiatric treatment (pharmacotherapy or psychotherapy),
• having a disease that prevents vision.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Supportive Care
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Intervention group; Light application	Other: Light application; Light application
Placebo Comparator: control group; Light application	Other: Light application; Light application

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
stress scale	QUESTIONNAIRE	2 minutes
anxiety scale	QUESTIONNAIRE	2 minutes

Collaborators and Investigators

• Sponsor: Osmaniye Korkut Ata University

Study record dates

Study Major Dates

• Study Start (Estimated): December 25, 2024
• Primary Completion (Estimated): December 30, 2024
• Study Completion (Estimated): January 15, 2025

Study Registration Dates

• First Submitted: December 5, 2024
• First Submitted That Met QC Criteria: December 15, 2024
• First Posted (Actual): March 25, 2025

Study Record Updates

• Last Update Posted (Actual): March 25, 2025
• Last Update Submitted That Met QC Criteria: December 15, 2024
• Last Verified: December 1, 2024

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Mental Disorders; Anxiety Disorders
• Other Study ID Numbers: 2053231

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO
• IPD Plan Description: Can be shared when necessary

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No