The Effect of Stress Ball on Labor Pain, Anxiety and Satisfaction in Labor
NCT ID: NCT06436859
Last Updated: 2024-05-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
48 participants
INTERVENTIONAL
2024-05-15
2025-05-15
Brief Summary
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H1 Using the Stress Ball in Labor reduces labor pain. H2 Using the Stress Ball in Labor Reduces Anxiety H3 Use of Stress Ball in Labor increases labor satisfaction.
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Detailed Description
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Utilizing non-pharmacologic and supportive methods to reduce labor pain is an important part of nursing/midwifery practices. Providing alternatives that allow women to make active decision-making to reduce pain management and anxiety during labor may affect pain, anxiety and hormonal oscillations. Currently, alternative strategies to reduce the use of medication during labor are being considered.
In line with the results of this study, it is thought that the stress ball may be effective in labor, where anxiety and pain are frequently experienced.
After obtaining all official permissions, it is planned to collect the data face-to-face. In the data collection phase, the researcher will first explain the purpose of the study to the women who meet the inclusion criteria and inform them about the study through written consent of the women will be obtained. When the women in the control and experimental groups are admitted to the delivery room, the Introductory Information ; will be collected by the researcher by face-to-face interview method. In addition,;State Anxiety Scale; will be administered during the first admission, VAS before cervical dilatation 0-3 cm, 3-8 cm and 8-10 cm and before placenta emergence, and ;State Anxiety Scale; will be administered when dilatation is 0-3 and 3-8 cm (at the beginning and end of the active phase of labor).;Birth Satisfaction Scale; will be administered in the first 24 hours after delivery before the patient is discharged. Data collection will be done similarly in both groups.
According to randomization, pregnant women in the intervention group will receive ;stress ball therapy; during labor.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Experiment
Stress ball group
stress ball group
According to randomization, pregnant women in the intervention group will receive "stress ball therapy" during labor.
Control group
Routine care
No interventions assigned to this group
Interventions
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stress ball group
According to randomization, pregnant women in the intervention group will receive "stress ball therapy" during labor.
Eligibility Criteria
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Inclusion Criteria
* Having a single, healthy fetus in head position,
* Applying during the latent phase of labor (cervical dilatation between 0-3 cm), .To give birth vaginally.
Exclusion Criteria
* Having a gestational or chronic disease,
* Having an obstacle to giving birth vaginally,
* Suspicion of fetal anomaly,
* Not volunteering to work,
* Women under the age of 18,
* Women who are illiterate in Turkish,
* Decision to perform caesarean section during labor,
* The participant wishes to withdraw from the research,
* Development of fetal distress,
* Using vacuum or forceps during birth, .Women with vision, hearing or mental problems.
18 Years
35 Years
FEMALE
Yes
Sponsors
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Öznur Hayat Öktem
OTHER
Responsible Party
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Öznur Hayat Öktem
PhD student
Locations
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Karabuk Training and Research Hospital, obstetrics clinic
Karabük, , Turkey (Türkiye)
Countries
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Central Contacts
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Facility Contacts
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PhD student Öznur HAYAT ÖKTEM, Phd Student Msc Midwife
Role: primary
Other Identifiers
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Hayatoktem03
Identifier Type: -
Identifier Source: org_study_id
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