- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06229808
The Effect of the Multifunctional Birthing Ball on Labor Pain
New Design; Investigation of the Effect of Multifunctional Birthing Ball on Perineal and Sacral Pain and Duration of Labor in the First Two Stages of Labor
Objective: By using the newly designed multifunctional birthing ball, it is aimed to reduce the intense perineal and sacral pain in the first and second stages of labor, to prevent perineal tears, pain and episiotomy opening with perineal heating, to take advantage of the positive effects of the birthing ball on the pelvis to support active labor and shorten the duration of labor, and to increase the satisfaction of mothers with labor by reducing anxiety and pain.
Materials and Methods: The multifunctional birthing ball will support the active movements of the pregnant woman, as well as warming the perineum while providing lumbar and back massage. The multifunctional birthing ball was developed by researchers and manufactured by the Near East University 3D Lab. The bottom of the ball is made of flexible and explosion-proof material filled with air. The purpose of the ball is to enable the pregnant woman to make swinging and bouncing movements during active labor. The massager and heating pad will be controlled by a single electronic circuit. Three different massage modes can be selected: continuous, intermittent and fluctuating. The heating pad can be turned on and off with a single button and the temperature can be adjusted (decrease-increase). To prevent overheating and tissue damage, a maximum temperature of 42 °C was fixed on the control. The inner padding is made of a material that protects both the massager and the heating pad from external factors and also serves as a seat. The shape of the device is designed to ensure that the massager is in full contact with the waist when the pregnant woman sits on the ball. The coating of the massage chair and heating pad is made of cleanable material suitable for hospital use.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study was designed to experimentally investigate the effect of a multifunctional birthing ball on perineal pain, sacral pain, total duration of labor, perineal tears, and women's satisfaction with the birth experience during the first and second stages of labor in pregnant women who will deliver vaginally. Pregnant women to be included in the experimental and control groups should meet the following criteria:
- First-time mothers
- At term (37-42 weeks of gestation)
- Single fetal gestation
- Cervical dilatation of 3 cm or greater
- Expected spontaneous delivery
- No pregnancy complications or systemic diseases
- No history of cephalopelvic disproportion, placenta previa, placental abruption, or fetal distress
- Willingness to participate in the study
- Age between 18 and 35 years
Experimental Intervention Participants in the experimental group will receive massages using a multifunctional birthing ball during the first stage of labor. Massages will be administered for 30 minutes each at the end of the latent, active, and transition phases (cervical dilatation 3-4 cm, 5-7 cm, and 8-10 cm, respectively). Visual Analog Scale (VAS) scores will be evaluated three times in each phase to assess low back pain. In the control group, VAS scores will be evaluated three times without massage application for the same periods.
Perineal Heating Application
Perineal heating application will be initiated when the second stage of labor begins and will continue until delivery. The heating application will consist of 20 minutes of application followed by 20 minutes of tissue rest. VAS scores will be evaluated two times during these stages to determine perineal pain. In the control group, VAS scores will be evaluated twice without heating application for the same periods.
Postpartum Evaluation
During the postpartum period, each participant will complete a 30-question "Postpartum Interview Form" that will address questions related to the status of perineal integrity at the end of labor, overall childbirth experience, and satisfaction with the birth process. Additionally, each participant will complete the "Birth Satisfaction Scale" - a 30-item questionnaire designed to assess the woman's satisfaction with her birth experience.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Nicosia, Cyprus
- Near East University
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- First-time mothers
- At term (37-42 weeks of gestation)
- Single fetal gestation
- Cervical dilatation of 3 cm or greater
- Expected spontaneous delivery
- No pregnancy complications or systemic diseases
- Age between 18 and 35 years
Exclusion Criteria:
- Non-pregnancy related chronic illness
- Pregnancy-related illness
- Pregnancy complications
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control group
No intervention will be applied
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Experimental: Multifunctional Birthing Ball group
Massages will be applied to the experimental group in the first stage of labor for 30 minutes each at the end of the latent, active and transition phases (cervical dilatation 3-4 cm, 5-7 cm, 8-10 cm), respectively. Perineal heating application is planned to be performed at least twice until the delivery occurs as 20 minutes of application and 20 minutes of tissue rest periods when the second stage of labor begins (the duration of this stage may reach 2 hours in primiparous women). |
In order to reduce low back pain in labor, massages will be applied to the experimental group in the first stage of labor for 30 minutes each at the end of the latent, active and transition phases (cervical dilatation 3-4 cm, 5-7 cm, 8-10 cm), respectively. Perineal heating application is planned to be performed at least twice until the delivery occurs as 20 minutes of application and 20 minutes of tissue rest periods when the second stage of labor begins (the duration of this stage may reach 2 hours in primiparous women). |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evaluating pain scores by performing lumbar massage with the massage chair on the birthing ball in order to reduce the back pain experienced during birth.
Time Frame: during the intervention
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In order to reduce the back pain experienced during birth, the experimental group received massages in the first stage of birth, respectively; It will be applied for 30 minutes at the end of the latent, active and transition phases (cervical dilatation 3-4 cm, 5-7 cm, 8-10 cm).
To determine low back pain at birth, VAS (visual analogue scale) scores will be evaluated a total of three times at all these stages.
In the control group, VAS scores will be evaluated three times without massage application for the same period of time.
|
during the intervention
|
|
Evaluating perineal pain with perineal heating application
Time Frame: during the intervention
|
Perineal heating application is planned to be performed at least twice when the second phase of labor begins (in primiparas, this phase may last up to 2 hours), with a 20-minute application and a 20-minute tissue rest period until birth.
To determine perineal pain, VAS (visual analogue scale) scores will be evaluated twice in all these stages.
In the control group, VAS scores will be evaluated twice at the same time without heating.
|
during the intervention
|
|
Applying the "Birth Satisfaction Scale" to measure the woman's satisfaction with her birth experience in the postpartum period.
Time Frame: immediately after the intervention
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Finally, in the postpartum period, the "Birth Satisfaction Scale" consisting of 30 items will be filled in to measure the woman's satisfaction with her birth experience.
The original "Birth Satisfaction Scale (BSS)" was developed by Caroline Hollins in 2009.
A Turkish validity and reliability study was conducted by Cosar Cetin F. and his colleagues in 2015.
Responses to this scale, which is a 5-point Likert type; Absolutely I agree.
5; I agree.
4; I'm undecided 3; Disagree 2; Strongly Disagree: scores as 1.
In the scale items; Items 4, 8, 12, 15, 16, 17, 19, 20, 21, 23, 25, and 29 are scored as reversed items.
The total number of points to be obtained from the scale varies between 30 and 150 points.
Subthemes in the scale were determined as quality of care, birth environment, adequate support and relationships with health professionals.
High scores from the scale indicate that the woman is more satisfied with birth.
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immediately after the intervention
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- YDU/2021/93-1378
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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