Dim lights may boost labor: simple trick to avoid C-Sections?
NCT ID NCT04521972
First seen Jun 25, 2026 · Last updated Jun 26, 2026 · Updated 2 times
Summary
This study tests whether adjusting room light during labor can improve uterine contractions and reduce the need for C-sections. Researchers will monitor 100 pregnant women, using different light settings (bright, dim, or red light) to see how it affects contractions and melatonin release. The goal is to find a simple, non-drug way to make labor more successful.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- room light manipulation (device)
- What this could lead to
- If it works, this could point toward a simple, drug-free way to improve labor success and reduce C-sections.
- What could go wrong
- This is a small, early study with only 100 participants, so results may not apply to all women. The effect of light on contractions is still uncertain.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Sep 2025
- Expected to finish
-
Sep 2029
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 42 years
- Sex
-
Female participants only
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria: * Are pregnant * Are 18-42 years old * Medically cleared for participation by Medical Investigator * Willingness to allow the study access to information in the participant's medical record * Willingness to be notified of incidental findings from study procedures * Willingness to measure and report on lighting conditions during specified time periods * Willingness to use a uterine contraction home monitor system, and report results * Willingness to adapt lighting during studies in home and/or hospital * Willingness to wear blue-filter glasses if requested * Willingness to report use of melatonin (for sleep) * Willingness to stop melatonin use if requested Exclusion criteria * Pre-pregnancy BMI \>36kg/m2 * HIV or AIDS (self-reported) * Severe anemia (hemoglobin \<8g/dL and/or hematocrit \<24%) * History or current psychotic disorder or diagnosis of a current major depressive episode or bipolar disorder * Current use of one or more of the following medications: metformin, systemic steroids, antipsychotic agents (e.g., Abilify, Haldol, Risperdal, Seroquel, Zyprexa), anti-seizure medications or mood stabilizers that would be expected to have a significant impact on body weight (e.g., Depakote, Lamictal, Lithium, Neurontin, Tegretol, Topamax, Keppra), medications for ADHD including amphetamines and methylphenidate * Continued use of weight loss medication including OTC and dietary supplements for weight loss (e.g., Adipex, Suprenza, Tenuate, Xenical, Alli, conjugated linoleic acid, Hoodia, Green tea extract, Guar gum, HydroxyCut, Sensa, Corti-slim, Chromium, chitosan, Bitter orange) Other Exclusion Criteria * Recent history of or currently smoking, drinking alcohol or abusing drugs (prescription or recreational) * Plans to move out of the study area within the next year or plans to be out of the study area for more than 8 weeks in the next 12 months * Planned termination of pregnancy
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Labor; poor are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Michigan State University
RECRUITINGEast Lansing, Michigan, 48824, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can Mom's workout shape Baby's heart health?
- Can a TB infection leave a mark on the placenta?
- Can a newer hepatitis b drug protect babies while being gentler on their bones?
- Can virtual mindfulness groups support pregnant individuals at risk?
- Can surveillance catch birth defects early in HIV-Affected pregnancies?
- Could a smartphone program ease pregnancy stress?