NCT07104071

Brief Summary

This study aims to determine the effects of light brightness on postpartum mothers' well-being, breastfeeding motivation, and psychological well-being. This study is a randomized, placebo-controlled study.

Trial Health

35
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
42

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Aug 2025

Status
not yet 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

First Submitted

Initial submission to the registry

July 29, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

August 5, 2025

Completed
10 days until next milestone

Study Start

First participant enrolled

August 15, 2025

Completed
7 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 22, 2025

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 23, 2025

Completed
Last Updated

August 5, 2025

Status Verified

July 1, 2025

Enrollment Period

7 days

First QC Date

July 29, 2025

Last Update Submit

July 29, 2025

Conditions

Reduced Light Brightness

Keywords

peaceswell-beingbreastfeeding

Outcome Measures

Primary Outcomes (3)

  • peace scala

    peace

    12 hours

  • well-being scala

    well-being

    12 hours

  • breastfeeding motivation scala

    breastfeeding motivation

    12 hours

Study Arms (2)

Intervention group

EXPERIMENTAL

reduced light brightness

Other: reduced light brightness

control group

NO INTERVENTION

No intervention

Interventions

reduced light brightnessOTHER

reduced light brightness

Intervention group

Eligibility Criteria

Age18 Years - 45 Years
Sexfemale(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • being postpartum mothers.

You may not qualify if:

  • having communication problems

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Breast Feeding

Condition Hierarchy (Ancestors)

Feeding BehaviorBehavior

Central Study Contacts

Emine E Yıldırım, Assistant Professor

CONTACT

+905066268672eminekucukyildirim@gmail.com

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Assistant professor

Study Record Dates

First Submitted

July 29, 2025

First Posted

August 5, 2025

Study Start

August 15, 2025

Primary Completion

August 22, 2025

Study Completion

August 23, 2025

Last Updated

August 5, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share