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

Osmaniye Korkut Ata University

Status: Not yet enrolling

Conditions: Light; Pregnant Women; Stress

Treatments: Other: Light intervention

Study type: Interventional

Funder types: Other

Identifiers

NCT06736873

205323

Details and patient eligibility

About

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.

Enrollment: 100 estimated patients

Sex: Female

Ages: 18 to 45 hours old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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100 participants in 2 patient groups, including a placebo group

light application

Experimental group

Description:

Non-stress test was performed under 100 lx light application.

Treatment:

Other: Light intervention

control group

Placebo Comparator group

Description:

Non-stress test was performed under 440 lx light application.

Treatment:

Other: Light intervention