Not yet recruiting NCT07104071
Effect of Light Brightness on Well-being, Breastfeeding Motivation, and Psychological Well-being of Postpartum Mothers: A Randomized Placebo-controlled Trial
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 brightness.
- Who it may be relevant to
- Registry conditions: Reduced Light Brightness. 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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Overview
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.
Interventions
- Other reduced light brightness
reduced light brightness
Primary outcome measures
- peace scala [Time frame: 12 hours]
- well-being scala [Time frame: 12 hours]
- breastfeeding motivation scala [Time frame: 12 hours]
Eligibility criteria
Inclusion criteria
- being postpartum mothers.
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: NCT07104071 · 131313