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Effect of Light Color on Stress, Anxiety, and Psychological Well-being During Nonstress Test in Pregnant Women at Risk

Effect of Light Color on Stress, Anxiety, and Psychological Well-being During Nonstress Test in Pregnant Women at Risk: A Randomized Placebo-controlled Study

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06736873
Enrollment
100
Registered
2024-12-17
Start date
2024-12-25
Completion date
2025-01-15
Last updated
2024-12-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Light, Pregnant Women, Stress

Brief summary

Purpose of the research: To determine the effect of light color on stress, anxiety, and psychological well-being during the Nonstress Test in at-risk pregnant women. This research was planned as a single-blind randomized controlled experimental type study by comparing separate groups in the form of experiment-placebo control. Data will be collected with the Introductory Information Form, Psychological Well-being Scale, Perceived Stress Scale (PSS/PSS-14), State Trait Anxiety Inventory (STAI). The NST device is used to follow up pregnant women in the last 3 months of pregnancy, first monthly, then every two weeks and once a week. In other words, the procedure is routinely performed on every pregnant woman who comes for control. It is a device that shows the well-being of the baby and whether the mother has contractions. It is attached to the pregnant woman's abdominal area and does not cause any harm. It is not an invasive procedure. Pregnant women in the last 3 months of pregnancy who come to have NST for follow-up will be randomly selected and divided into 2 groups. A lamp with adjustable light level with Unit Unit Ut-383 Mini Luxmeter (Light Meter) will be placed in the intervention and control groups and the light level of the lamp will be adjusted to 100 lux. NST will be taken under cold (bluish white) light for the control group and under medium warm white (daylight white) light for the intervention group. Pre-test before the application and post-test after the application will be applied. The application is an invasive application that will not disturb the pregnant woman.

Interventions

Light intervention

Sponsors

Osmaniye Korkut Ata University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Hours to 45 Hours
Healthy volunteers
Yes

Inclusion criteria

* Being at risk of pregnancy, * being in the last trimester of pregnancy, * being a volunteer.

Exclusion criteria

* Having any problem that prevents communication (such as not knowing Turkish, having hearing, speaking and understanding disorders), * being on psychiatric treatment (pharmacotherapy or psychotherapy), * having a disease in their eyes that prevents them from seeing

Design outcomes

Primary

MeasureTime frameDescription
stress scale2 minutesquestionnaire
anxiety scale2 minutesquestionnaire
psychological well-being scale1 minutesquestionnaire

Contacts

Primary ContactEmine Yıldırım, Assistant Professor
eminekucukyildirim@gmail.com05066268672
Backup ContactFiliz POLAT
filizmermer@yahoo.com05066268672

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026