An interventional study of Light intervention in Pregnant Women, Stress and Light, sponsored by Osmaniye Korkut Ata University. Not yet recruiting. Open to female participants aged 18 Hours to 45 Hours, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-12-17.
Sponsored by Osmaniye Korkut Ata University · Not applicable, Interventional, and Supportive care
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.
Osmaniye Korkut Ata University is the lead sponsor of 35 studies on the registry; 7 are open to participants now.
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Exclusion Criteria:
Non-stress test was performed under 100 lx light application.
Other: Light intervention
Non-stress test was performed under 440 lx light application.
Other: Light intervention
Light intervention
stress scale
questionnaire
Time frame: 2 minutes
anxiety scale
questionnaire
Time frame: 2 minutes
psychological well-being scale
questionnaire
Time frame: 1 minutes
No study locations are listed for this record.
Plan to share: No — Can be shared when necessary.
No publications or documents are linked to this record.
Start is estimated for Dec 2024; primary completion for Dec 2024, 0 months later.
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This study is not yet recruiting, as verified in Dec 2024. You cannot join it, but the record below documents what was studied.
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Osmaniye Korkut Ata University