- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06155435
INVESTIGATION OF THE EFFECT OF SOLUTION-FOCUSED APPROACH TRAINING ON TRAUMATIC BIRTH PERCEPTION, VAGINAL BIRTH SELF-EFFICACY AND BIRTH TYPE PREFERENCE.
THE EFFECT OF SOLUTION-FOCUSED APPROACH TRAINING GIVEN TO NULLIPAROUS PREGNANT WOMEN ON TRAUMATIC BIRTH PERCEPTION, VAGINAL BIRTH SELF-EFFICACY AND BIRTH TYPE PREFERENCE
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Tuğba Yazıcı Topçu
- Phone Number: +905535718551
- Email: tibiyzc@gmail.com
Study Locations
-
-
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Trabzon, Turkey
- Recruiting
- Karadeniz Teknik Üniversitesi
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Contact:
- Tuğba Yazıcı Topçu
- Phone Number: +905535718551
- Email: tibiyzc@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Agreeing to participate in the research
- Being over 20 years old
- Being able to speak Turkish
- Not having any disability such as hearing or vision
- Being nulliparous pregnant
- Being in the 3rd trimester (those who are pregnant between 28-35 weeks)
- Not having received any psychiatric diagnosis before
- No risk of vaginal bleeding, hypertension, diabetes, multiple pregnancy etc. during pregnancy.
- Not having any physical/mental problems that would prevent normal birth.
Exclusion Criteria:
- Pregnant women in high risk groups (arthritis, premature birth, placenta previa, etc.)
- Multigravida pregnant women (pregnant women with 2 or more pregnancies)
- Having received any psychiatric diagnosis and/or receiving psychiatric treatment.
The termination criteria for the cases included in the study will be as follows:
- Intrauterine fetal death during pregnancy,
- Emergence of any risk during pregnancy,
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: experimental group
Firstly, the Pregnant Information Form, Traumatic Birth Perception Scale and Vaginal Birth Self-Efficacy Scale forms will be applied.Solution-oriented approach training; It is indicated for pregnant women one by one and in the form of at least 4 entries. A recording will take approximately 30-35 minutes.15-21 days after the solution-oriented approach training is completed the traumatic birth perception and vaginal birth self-efficacy scale form will be applied again.The traumatic birth perception form will be applied again 15-21 days after birth. The woman's birth type will be learned and recorded. 40 pregnant women will be followed in the experimental group. |
To the woman; A list of education subjects will be sent in order to determine educational changes for birth, birth and postpartum periods.
This list will be; It consists of reproductive organs, pregnancy formations, changes, psychological changes, daily life, nutrition, reproductive monitoring, immunization, frequent problems and solution suggestions, danger signs and what to do.
Also included in the list are labor, birth cycle, and postpartum periods.
Other Names:
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No Intervention: control group
Firstly, the Pregnant Information Form, Traumatic Birth Perception Scale and Vaginal Birth Self-Efficacy Scale forms will be applied.
will be no intervention on the pregnant women in the control group, and the 15-21st week after the prenatal care given to the pregnant women by the Ministry of Health is completed.
Traumatic birth perception and vaginal birth self-efficacy scale form will be filled in on these days.
The traumatic birth perception form will be applied again 15-21 days after birth.
The woman's birth type will be learned and recorded.
40 pregnant women will be followed in the control group.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
traumatic birth perception scale
Time Frame: two months
|
It was developed to measure the traumatic birth perception levels of women of reproductive age.
There are a total of 13 questions in the scale.
These questions; It includes the feelings and thoughts, anxiety, fear and trauma that a woman may experience when she thinks about giving birth.
Answers to the questions were scored between 0 and 10, from "none at all" to "most".
The total score obtained from the scale shows the level of perception of traumatic birth.
The minimum scores that can be obtained from the scale are 0 and the maximum is 130.
Total score averages indicate that the 0-26 point range is very low, the 27-52 point range is low, the 53-78 point range is medium, the 79-104 point range is high, and the 105-130 point range indicates that the woman has a very high level of perception of traumatic birth.
The Cronbach Alpha reliability coefficient of the scale is 0.895.
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two months
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vagınal bırth self-effıcacy
Time Frame: two months
|
This scale was developed to measure self-efficacy regarding vaginal birth during pregnancy.
The scale consists of 9 items and there is an 11-point (0-10) numerical rating scale for each item.
Scores range from 0 to 90, with higher scores indicating higher levels of self-efficacy.
There are no items in the scale that need to be reverse coded.
Cronbach's alpha coefficient, as a reliability criterion to determine the internal consistency of the scale, varies between 0.93 and 0.94.
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two months
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KTU-SABE-TYT-01
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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