- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06791252
Genital Hygiene Education and Pregnancy
The Effect of Genital Hygiene Education Given to Pregnant Women Diagnosed with Urinary Tract Infection on Genital Hygiene Behavior and Self-Care Agency
Genital hygiene behaviors are of great importance in preventing urinary tract infections, especially during pregnancy. The study was conducted to determine the effect of genital hygiene education given to pregnant women diagnosed with urinary tract infections on genital hygiene behavior and self-care ability. The hypotheses of this study were determined as follows:
H1a: Genital hygiene education affects genital hygiene behavior in pregnant women.
H1b: Genital hygiene education affects self-care ability in pregnant women.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Malatya, Turkey
- Malatya
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- All pregnant women who were literate, - Who had completed their pharmacological treatment (antibiotic treatment) for UTI according to medical records were included in the sample
Exclusion Criteria:
- - Those who had previously received training to increase genital hygiene behavior,
- Those who had a risky pregnancy,
- Those who were diagnosed with any health problems related to the pregnant woman and the fetus were not included in the study
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Group receiving genital hygiene education
Pregnant women in the experimental group were given genital hygiene training in 4 sessions.
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The pregnant women in the experimental group were given genital hygiene training individually and in their own homes by the researcher. During the training, the privacy of the client was observed and the researcher and the pregnant women were left alone in the room where the training would be given. Care was taken to ensure that the environment was quiet and calm while the training was given. It was preferred that the pregnant women be in the most comfortable position during the training. The training was completed by explaining each topic in the training booklet in an average of 20-25 minutes. Genital hygiene training content: Session 1 (Day 1): After the introduction phase, information was given about the method to be followed in the study to the pregnant women who agreed to participate in the study. Then, the "Minimum Informed Consent Form" was given to these women, and the pregnant women who approved the form after reading it were included in the study. Pre-test data were collecte |
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No Intervention: Control Group
No intervention was applied to the control group other than the application of data collection tools simultaneously with the pregnant women in the experimental group (pre-test: 1st session/1st day - post-test: 2nd session/30th day).
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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genital hygiene behavior
Time Frame: 30 days
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Considering that behaviors regarding genital hygiene are established from an early age, it is important to objectively determine risky behaviors in young women who are not yet sexually active in order to take precautions for improving genital hygiene.In this way, many negative outcomes that may occur during the fertile period and are directly related to genital infections, such as infertility, abortion, and the threat of premature birth,can be prevented.On the other hand, it would be useful to use an objective, valid, and reliable measurement tool in determining the relationship between genital hygiene behaviors in women and situations such as the threat of premature birth, premature rupture of membranes, and postpartum infection.The primary outcome of this study is to determine the genital hygiene behaviors of the hygiene education given to women who have previously had urinary tract infections.For this purpose, the General Hygiene Habit and Abnormal Finding Awareness scale was used.
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30 days
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Self-Care Ability
Time Frame: 30 days
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Self-care is the activities initiated and carried out by an individual to protect, maintain and improve their life, health and well-being.
According to Orem, self-care needs are divided into three groups: universal, developmental and self-care needs in deviations from health.
Universal needs are special care behaviors that occur at different developmental levels of the individual, such as infancy, childhood and pregnancy.
Pregnancy is also a developmental condition and is a subject that should be examined separately due to its importance.
During pregnancy, a woman may need help if her health deteriorates and she cannot meet her care needs.
It is important to use an objective, valid and reliable measurement tool in determining the relationship between the self-care of pregnant women and conditions such as urinary system infections.
In this study, self-care power was determined as a secondary outcome and the self-care power scale was used to determine the effect of hygiene training give
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30 days
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Collaborators and Investigators
Sponsor
Publications and helpful links
Helpful Links
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 (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2021/2261
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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