Application of Stress Ball and Non-stress Test With Pregnant Women

Kırklareli University

Status

Completed

Conditions

Pregnancy Related

Anxiety

Treatments

Other: stress ball

Study type

Interventional

Funder types

Other

Identifiers

NCT05626218

KırklareliAS-7

Details and patient eligibility

About

This research was planned as a randomized controlled experimental study to reduce the anxiety expectant mothers feel when on a non-stress test.

Full description

Fetal well-being is assessed by evaluating fetal heart rate (FHR) patterns. The primary aim is to identify fetuses at risk of intrauterine death or neonatal complications and, if possible, intervene (usually by delivery) to prevent these adverse outcomes. The most commonly used method for this purpose is the non-stress test. Non-stress test (NST) is a non-invasive fetal evaluation method. The NST is evaluated for at least 20 minutes while the expectant mother is lying supine or left-side.

Although it is a painless procedure, it takes about 20 minutes, and the pregnant woman stays in the same position throughout the procedure, creating although there are many methods to reduce stress, it is thought that a cheap and easily accessible stress ball can be used as a method of distraction or distraction. Although there are studies investigating the effectiveness of stress balls in managing various disease groups and symptoms in the literature, no study has been found to examine the NST effectiveness of stress balls. This research was planned as a randomized controlled experimental study to reduce the stress felt by women who had a non-stress test during pregnancy by applying a stress ball during the procedure. anxiety for the pregnant woman. The fact that the pregnant woman has high anxiety during the procedure affects the test result and may increase the false-positive rate and cause false evaluation. This increase in the false-positive rate in NST results may lead to an increase in an operative delivery. However, it is the midwives' responsibility to eliminate the situations that cause anxiety in pregnant women, which may affect the NST result before and during the procedure.

Enrollment

80 patients

Sex

Female

Ages

20 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Ability to read and understand Turkish
Being between the ages of 20-35
Single pregnancy
Having had NST before

¬- Have eaten at least 2 hours before the NST procedure
Don't be primiparous
Getting 37 or less on the trait anxiety (STAI-1) scale
Getting 37 or more on the state anxiety (STAI-2) scale
Volunteering to participate in the research
Fully answering survey and scale forms
Being in the 3rd trimester

Exclusion criteria

Having been diagnosed with a risky pregnancy
Unwilling to continue working
Having a chronic disease (Diabetes, Hypertension, Thyroid etc.),
Having any problem that prevents communication (such as hearing, speaking, and understanding abilities),
Using one of the pharmacological or non-pharmacological methods to reduce stress and receiving psychiatric treatment (Pharmacotherapy or psychotherapy).