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临床试验/NCT06736873
NCT06736873尚未招募不适用

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

Osmaniye Korkut Ata University0 个研究点目标入组 100 人开始时间: 2024年12月25日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
100
主要终点
stress scale

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Participant)

入排标准

年龄范围
18 Hours 至 45 Hours(Child)
性别
Female
接受健康志愿者
是

入选标准

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

排除标准

  • •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

研究组 & 干预措施

light application

Experimental

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

干预措施: Light intervention (Other)

control group

Placebo Comparator

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

干预措施: Light intervention (Other)

结局指标

主要结局

stress scale

时间窗: 2 minutes

questionnaire

anxiety scale

时间窗: 2 minutes

questionnaire

psychological well-being scale

时间窗: 1 minutes

questionnaire

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Emine Yıldırım

Assistant professor

Osmaniye Korkut Ata University

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