In the first part of the study, pregnant women who apply to Kahramanmaraş Sütçü İmam University Health Practice and Research Hospital Obstetrics and Gynecology Outpatient Clinic and are referred to NST and meet the inclusion criteria will be informed about the project and verbal and written consent will be obtained. In this direction, survey questions will be directed to pregnant women who agree to participate in the study. In the study, pre-test data will be obtained with 13-question Participant Introduction Form and 20-question State Anxiety Scale forms. Post-test data will be obtained after the NST procedure is completed for the experimental groups, the researcher will ask the State Anxiety Scale, VAS-Satisfaction form by face-to-face interview method and the NST Findings Record Form will be filled by the researcher.
and the explanations made to the pregnant women before the procedure will be made in a room outside the NST room.
Randomization Pregnant women included in the study will be randomized with the single-blinded randomized rule. Randomization will be done by using the random integer generator method in the numbers subheading of the random.org website, and three-group columns will be created with numbers from 1 to 108. At the beginning of the study, lots will be drawn to determine which of the 3 columns will be the experimental groups and which will be the control group. When there is a participant who meets the inclusion criteria, the participant will be included in whichever group the next number is in.
Data Collection Tools Data will be collected using the Personal Introduction Form, which determines the socio-demographic and obstetric characteristics of women and their knowledge about NST, the State Anxiety Scale, the NST Findings Record Form, which includes the findings related to NST, which allows the researchers to evaluate the NST result of pregnant women, and the Visual Analog Scale (VAS) - Satisfaction Form to evaluate their satisfaction after NST.
Personal Introduction Form This form was created by the researchers to determine women's sociodemographic (age, educational status, etc.), obstetric characteristics (pregnancy, abortion and number of living children) and knowledge about NST (receiving information about NST before, from whom they received the information, reason for NST withdrawal, etc.).
State Anxiety Scale (SAS) The adaptation of the State-Trait Anxiety Scale, which was developed by Spielberg et al. in 1970 to measure anxiety level, into Turkish was performed by Öner and Le Compte (1983). The scale consists of two parts and the State Anxiety part was used in this study. There are 20 statements in the scale . The scales include both direct statements and inverted statements. While direct statements express negative emotions, inverted statements reflect positive emotions. In the State Anxiety Scale, these reversed statements are items numbered 1, 2, 5, 8, 10, 11, 15, 16, 19 and 20. The statements in the scale are answered by marking (1) not at all, (2) a little, (3) a lot, and (4) completely in order to evaluate emotions or behaviors according to the severity of the experiences. The total score obtained varies between 20 and 80. A high score on the scale indicates a high level of anxiety. The Cronbach alpha value of the scale was found between 0.94 and 0.96 .
NST Findings Record Form The NST Findings Record Form is a form used by researchers to evaluate the NST results of pregnant women. This form contains data in which the findings of NST of pregnant women are recorded .
Evaluation of the NST Findings Record Form; NST results of pregnant women were evaluated by the researchers. As reactive NST, the result of the test will be accepted as reactive NST in the presence of at least two accelerations lasting at least 15 seconds and 15 beats/minute more than the baseline beat within 20 minutes of electronic fetal heart rate tracings . As nonreactive NST, the result of the test will be considered as nonreactive NST in the absence of at least two accelerations lasting at least 15 seconds and lasting more than 15 beats/min more than the baseline beat within 20 minutes of printing electronic fetal heart rate tracings, in the presence of severe variable deselerations and late deselerations, or in the development of continuous fetal tachycardia of 160 beats/min or more when the baseline tracings are normal .
Visual Analog Scale (VAS)- Satisfaction Form The scale developed by Price et al. (1983) is a very simple, easy-to-administer measurement method used to measure subjective experiences. It is a measurement tool that is evaluated by individuals marking a horizontal or vertical line of 10 cm or 100 mm, with one end indicating "very good" and the other end indicating "very bad". This line is only straight
