The Effect of Stress Ball Application on Anxiety and Fetal Heart Rate Before Cesarean Section
1 other identifier
interventional
88
1 country
1
Brief Summary
This study will be conducted to determine the effect of stress ball application on anxiety and fetal heart rate in risk pregnant women before cesarean section. Women with risk pregnancies randomly assigned to intervention (n=44) and control (n=44) groups in a faculty hospital in Turkey will be included in the study. Pregnant women in the intervention group will be instructed how to use the stress ball in the obstetrics ward before cesarean section. During the practice, pregnant women will be asked to demonstrate the movements of tightening and loosening the stress ball to ensure correct use. It will be emphasized to the pregnant women that they should squeeze the ball once after counting to three, inhale when they squeeze the ball, exhale when they loosen their grip and focus only on the ball. Pregnant women in the control group will not receive any intervention other than routine general care. Data will be collected face-to-face by the researcher based on the self-reports of the pregnant women before cesarean section.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Oct 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 14, 2024
CompletedFirst Posted
Study publicly available on registry
October 17, 2024
CompletedStudy Start
First participant enrolled
October 30, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
June 15, 2025
CompletedJuly 30, 2025
July 1, 2025
5 months
October 14, 2024
July 29, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
State-Trait anxiety score for anxiety
The anxiety scale developed by Spielberger et al. in 1970 was designed to measure state and trait anxiety levels of individuals. The Turkish version of this scale was evaluated by Öner and Le Compte in 1983 and its reliability and validity were determined. The scale examines anxiety in two different dimensions: State Anxiety measures the feelings of an individual under a certain moment and condition, while Trait Anxiety refers to the general anxiety level of the individual. Each statement in the scale is a 4-point Likert scale (1-none, 2-somewhat, 3-a lot, 4-completely). Two types of expressions are used in the Spielberger State-Trait Anxiety Scale. Direct expressions indicate negative emotions and inverted expressions indicate positive emotions. Items 1,2,5,8,10,11,15,16,19 and 20 in the Spielberg State Anxiety Scale (SSAS) and items 26,27,30,33,36 and 39 in the Spielberg Trait Anxiety Scale (SSAS) are inverted statements. During the evaluation, after the total weights of the direct
Anxiety levels will be assessed 5 minutes before intervention and 5 minutes after the end of the intervention.
Fetal heart rate
Fetal heart rate will be measured by fetal hand-held Doppler before and after the intervention.
Fetal heart rate levels will be assessed 5 minutes before intervention and 5 minutes after the end of the intervention.
Secondary Outcomes (3)
Pulse rate (beats/minute)
Pulse rate of pregnant women will be assessed 5 minutes before intervention and 5 minutes after the end of the intervention.
respiration rate (times/minute)
Respiration rate of pregnant women will be assessed 5 minutes before intervention and 5 minutes after the end of the intervention.
systolic and diastolic blood pressure (mmHg)
Systolic and diastolic blood pressure of pregnant women will be assessed 5 minutes before intervention and 5 minutes after the end of the intervention.
Study Arms (2)
Control Group
NO INTERVENTIONPregnant women in the control group will not receive any intervention other than routine general care before cesarean section.
Intervention Group
EXPERIMENTALPregnant women in the intervention group will be explained how to use the stress ball in the obstetric ward before cesarean section. During the practice, pregnant women will be asked to demonstrate the movements of squeezing and loosening the stress ball to ensure correct use. It will be emphasized to the pregnant women that they should squeeze the ball once after counting to three, inhale when they squeeze the ball, exhale when they loosen their grip and focus only on the ball. In the obstetrics ward, this practice will cover the period starting from the time when the patient is waiting in her room to be taken to the operating room for cesarean section, until she is taken from the preop room to the operating room. In this process, the researcher will monitor whether the stress ball is applied correctly or not. In addition, in order to minimize the risk of infection in the hospital environment, the stress balls used will be disinfected with disposable aseptic wipes before being given
Interventions
The stress ball is a simple and effective tool for reducing anxiety and relaxation as a non-pharmacological method (Yanes et al., 2018). Due to the limited pharmacological options available for pregnant women to reduce anxiety during cesarean section, alternative, complementary or supportive non-pharmacological methods and low-risk approaches are needed (Baltacı \& Başer, 2020). It is thought that squeezing the stress ball may be advantageous in reducing anxiety.
Eligibility Criteria
You may qualify if:
- Volunteering to participate in the research,
- Be over 18 years of age,
- Having a medically diagnosed risky condition during pregnancy (diabetes, hypertension, threat of preterm labor, pre-eclampsia, etc.),
- Compliance with at least one of the criteria in the "Ministry of Health Risk Assessment Form for Pregnancy" in the evaluation of current pregnancy,
- Planning a cesarean delivery,
- Being in the last trimester of pregnancy (28 weeks and above)
- Having a single live fetus,
- To be able to read and write Turkish.
You may not qualify if:
- A diagnosed psychiatric illness,
- Visual, hearing, speech, physical or mental disability,
- Any communication barriers,
- Cardiovascular disease in the pregnant woman and fetus,
- Fetal distress,
- Fetal anomaly,
- Any physical or medical condition that prevents the use of a stress ball,
- Need for urgent intervention before caesarean section according to the physician.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ondokuz Mayıs University
Samsun, Atakum, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Nazlı BALTACI, Assoc. Prof.
baltacinazli@gmail.com
- PRINCIPAL INVESTIGATOR
Elif Eyüpoğlu
elifeyupogluu@gmail.com
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor, phD
Study Record Dates
First Submitted
October 14, 2024
First Posted
October 17, 2024
Study Start
October 30, 2024
Primary Completion
March 30, 2025
Study Completion
June 15, 2025
Last Updated
July 30, 2025
Record last verified: 2025-07