Effect of Reduced Light Color Temperature on Postpartum Mothers' Well-being, Breastfeeding Motivation, and Psychological Well-being After Cesarean Section
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Reduced light color temperature.
- Who it may be relevant to
- Registry conditions: Light Color Temperature. Basic parameters: 18 years — 45 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Effect of Reduced Light Color Temperature on Postpartum Mothers' Well-being, Breastfeeding Motivation, and Psychological Well-being After Cesarean Section: A Randomized Placebo-controlled Trial
Overview
The aim of this study is to determine the effects of reduced light color temperature on postpartum mothers' well-being, breastfeeding motivation, and psychological well-being after cesarean section. Method: This study is a randomized controlled experimental study conducted with 80 postpartum mothers. Data are collected using a Personal Information Form, the Well-being Scale (HS), the Psychological Well-being Scale (PWB), and the Breastfeeding Motivation Scale (BMS).
Interventions
- Other Reduced light color temperature
reduced light color temperature on postpartum mothers' well-being, breastfeeding motivation, and psychological well-being after a cesarean section
Primary outcome measures
- the Well-being Scale [Time frame: 12 hours]
- the Peace Scale [Time frame: 12 hours]
- Breastfeeding Motivation Scale [Time frame: 12 hours]
Eligibility criteria
Inclusion criteria
- being in the postpartum process
Exclusion criteria
- having communication problems
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Supportive care
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07104045 · 121212