- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05624060
Perineal Massage and Pelvic Floor Exercise in the Antenatal Period
January 16, 2025 updated by: Sultan OZKAN SAT, Bitlis Eren University
The Effect of Perineal Massage and Pelvic Floor Exercise Applied in the Antenatal Period on Postpartum Sexuality and Incontinence: a Randomized Controlled Study
This study aimed to determine the effect of perineal massage and pelvic floor exercise in the antenatal period on sexuality and urinary and fecal incontinence in the postpartum period.
This study will be conducted in a pregnant school at a state hospital in Turkey.
An active control group will be formed as the control group.
The control group will be given the "Pelvic Floor Dysfunction Prevention Training" booklet prepared by the researchers.
Experimental 1 group will receive perineal massage training in addition to the "Pelvic Floor Dysfunction Prevention Training" booklet given to the control group.
Experimental 2 group will receive pelvic floor exercises in addition to perineal massage training and the "Pelvic Floor Dysfunction Prevention Training" booklet given to the control group.
Study Overview
Status
Completed
Detailed Description
The research was conducted as a randomized controlled trial.
The simple randomization method will be used for the assignment to groups.
The data of the research; will be collected using the Preliminary Evaluation Form, Personal Information Form, Female Sexual Function Index, The International Consultation on Incontinence Questionnaire-ICIQ-SF (Turkish Version), and Fecal Incontinence Severity Index.
The research will start at the 34th week of pregnancy and the questionnaires will be administered in the 3rd month after delivery.
There will be 3 groups in the research.An active control group will be formed as the control group.
The control group will be given the "Pelvic Floor Dysfunction Prevention Training" booklet prepared by the researchers.
Experimental 1 group will receive perineal massage training in addition to the "Pelvic Floor Dysfunction Prevention Training" booklet given to the control group.
Experimental 2 group will receive pelvic floor exercises in addition to perineal massage training and the "Pelvic Floor Dysfunction Prevention Training" booklet given to the control group.
Study Type
Interventional
Enrollment (Actual)
75
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Karabük, Turkey
- Karabük Health and Training Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 49 years (Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- being over 18 years old,
- being 32-34th pregnancy weeks,
- being not experiencing any complications in the mother and fetus during pregnancy (gestational diabetes, hypertension, preeclampsia, intrauterine growth retardation, congenital anomaly, etc.),
- having a singleton pregnancy,
- being primiparous
- being volunteer to participate in the study
Exclusion Criteria:
- elective cesarean section planning,
- having a history of chronic constipation,
- having a previous history of urinary or anal incontinence,
- having genital infection with lesions (HSV, HPV, Syphilis, Candida Albicans, Chancroid)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
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 |
|---|---|
|
Active Comparator: Control Group
Pelvic Floor Dysfunction Prevention Training
|
The "Pelvic Floor Dysfunction Prevention Training" booklet is cover weight control, perineal hygiene, adequate fluid consumption, not smoking and alcohol use, avoidance of spicy, fizzy and fatty foods and beverages, correct posture and frequency of micturition, prevention of constipation and abdominal pressure.
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Experimental: Experimental Group 1
Pelvic Floor Dysfunction Prevention Training and Perineal Massage
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The "Pelvic Floor Dysfunction Prevention Training" booklet is cover weight control, perineal hygiene, adequate fluid consumption, not smoking and alcohol use, avoidance of spicy, fizzy and fatty foods and beverages, correct posture and frequency of micturition, prevention of constipation and abdominal pressure.
Women will apply perineal massage for an average of 8-10 minutes at least twice a week, starting from the 34th week of pregnancy until delivery.
In addition to perineal massage, the "Pelvic Floor Dysfunction Prevention Training" booklet will be given to participant.
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Experimental: Experimental Group 2
Pelvic Floor Dysfunction Prevention Training and Perineal Massage and Pelvic Floor Exercise
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The "Pelvic Floor Dysfunction Prevention Training" booklet is cover weight control, perineal hygiene, adequate fluid consumption, not smoking and alcohol use, avoidance of spicy, fizzy and fatty foods and beverages, correct posture and frequency of micturition, prevention of constipation and abdominal pressure.
Women will apply perineal massage for an average of 8-10 minutes at least twice a week, starting from the 34th week of pregnancy until delivery.
In addition to perineal massage, the "Pelvic Floor Dysfunction Prevention Training" booklet will be given to participant.
Women assigned to this group will apply pelvic floor exercise at least 3 days a week 8-12 times a week, starting from the 34th week of pregnancy until delivery.
In addition, women will apply perineal massage for an average of 8-10 minutes at least twice a week, starting from the 34th week of pregnancy until delivery.
In addition to perineal massage, the "Pelvic Floor Dysfunction Prevention Training" booklet will be given to participant.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Female Sexual Function Index
Time Frame: Postpartum 12th weeks
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In the structure of the scale; There are 6 sub-dimensions: desire, arousal, lubrication (lubrication, wetting), orgasm, satisfaction and pain.The highest raw score that can be obtained from the scale is 95 and the lowest raw score is 4.After sub-dimension averages were multiplied by factor loads, the highest score that could be obtained from the scale was calculated as 36 and the lowest score as 2. High score means better function.
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Postpartum 12th weeks
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The International Consultation on Incontinence Questionnaire-ICIQ
Time Frame: Postpartum 12th weeks
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The International Consultation on Incontinence Questionnaire-ICIQ-SF (Turkish Version) is a scale for evaluating every aspect of urinary incontinence and its impact on quality of life.It consists of 6 questions.The ICIQ Total Score is calculated by the sum of the 3+4+5 questions and scores between 0 and 21.
If the score is high and close to 21, it shows that it is overly affected.
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Postpartum 12th weeks
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Fecal Incontinence Severity Index-FISI
Time Frame: Postpartum 12th weeks
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It is an index developed to diagnose the frequency and type of fecal incontinence.It defines the type of fecal incontinence in four types and its frequency in five categories.
The index score is calculated by summing the numbers corresponding to each box and the patient score.
In patient-weighted scoring, the highest score that can be obtained from the index is 61 and the lowest score is 0.The cut-off score of the index is 31.7.
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Postpartum 12th weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Sultan Özkan Şat, Dr, Bitlis Eren University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 1, 2023
Primary Completion (Actual)
November 20, 2023
Study Completion (Actual)
November 20, 2023
Study Registration Dates
First Submitted
November 13, 2022
First Submitted That Met QC Criteria
November 13, 2022
First Posted (Actual)
November 21, 2022
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
January 16, 2025
Last Verified
November 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Urogenital Diseases
- Male Urogenital Diseases
- Urologic Diseases
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Intestinal Diseases
- Urination Disorders
- Lower Urinary Tract Symptoms
- Urological Manifestations
- Digestive System Diseases
- Gastrointestinal Diseases
- Rectal Diseases
- Urinary Incontinence
- Fecal Incontinence
Other Study ID Numbers
- SULTANOZKANSAT
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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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