- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06287658
The Effect of Kegel Exercise and Ba Duan Jin Applications on Premenopausal Women With Urinary Incontinence
April 1, 2024 updated by: Birsen ALTAY, Ondokuz Mayıs University
The Effect of Kegel Exercise and Ba Duan Jin Applications on Quality of Life and Psychological Well-Being Applied to Premenopausal Women With Urinary Incontinence
This study aimed to determine the effects of Kegel exercise and Ba Duan Jin applications applied to premenopausal women with urinary incontinence on quality of life and psychological well-being.
Study Group of the Research: Premenopausal women between the ages of 45-55 who come to the family health center with any complaint and have urinary incontinence.
The research will be conducted as a randomized pre-test, post-test and control group intervention study design.
The research will be conducted with women aged 45-55 with urinary incontinence who came for examination for any reason to a Family Health Center in Sinop between March 2024 and July 2024.
According to the power analysis, the number of participants was calculated to be at least 54 when the type 1 error was taken as 0.05, the power was 0.95 and the effect size was medium (0.25) for the two-group design with two repeated measurements.
To prevent possible data loss, the sample size was increased by 10% and the total number of participants was determined as 60.
A total of 60 women, 30 experimental and 30 control, coming to the Family Health Center will be randomly included in the study.
No information, Kegel exercise program and Ba Duan Jin applications will be given to the women in the experimental group, and no intervention will be given to the control group during the research process.
Participants will be assigned to 2 groups: experimental and control.
Those who come to FHC on odd days of the month will be included in the experimental group, and those who come on even days of the month will be included in the control group.
Each group will be determined as 30 people.
After the research is completed, the interventions applied to the experimental group will be applied to the women in the control group.
Personal Information Form, Psychological Well-Being Scale and Incontinence Quality of Life Scale will be applied to women in the experimental and control groups as pre-test measurements.
As a final test, the same measurements will be made to both the control group and the experimental group 16 weeks after the first measurement.
Study Overview
Status
Recruiting
Detailed Description
All applications regarding Kegel exercise and Ba Duan Jin applications have been determined.
Kegel exercise content; At the beginning of the exercise, one should try to hold urine while emptying the bladder only once or twice in order to define the pelvic floor muscles correctly.
If the result is successful, it means that the correct muscles contracted.
The second stage, the beginning of the exercise; It can be performed in a supine position (with legs bent at the knee) or in a sitting position.
The bladder should be emptied before starting exercise.
In the determined position, the pelvic floor muscles should be contracted for 5 seconds, as if stopping urine or gas outflow, and then relaxed for 5 seconds.
It should be repeated 4-5 times in a row.
The gluteal, abdominal and thigh muscles should not contract.
In this way, it is defined that the correct muscles are contracting.
In the Ba Duan Jin practice: stretch the hands to the sky, pull the arrow and string the bow (the knees are bent, the sitting posture on the horse is taken, the hand and arm take a stance as if pulling an arrow to the right and left alternately, eyes look at the target in the distance), push the sky and the earth ( Similar to the first movement, while raising the hands, one hand is directed upwards towards the sky and the other hand is directed towards the ground, turn the head and look back, shake the head and shake the tail (This movement regulates the functions of the heart and lungs, facilitates relaxation by relaxing the sympathetic nervous system, and helps emotional imbalances in the body).
It is said that it removes the stagnation of Qi and eliminates the numbness and malaise in the legs.
Its main purpose is to eliminate excessive heat in the heart), bending the waist down and holding the feet, punching, looking angry and shaking the ground by heeling will be done respectively.
Study Type
Interventional
Enrollment (Estimated)
60
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 Contact
- Name: Tuba YILMAZ BULUT, Dr.
- Phone Number: +905343435109
- Email: tuba_yilmaz1991@hotmail.com
Study Contact Backup
- Name: Birsen ALTAY, Ass. Prof.
- Phone Number: 0 (535) 546 54 53
- Email: baltay@omu.edu.tr
Study Locations
-
-
-
Kocaeli, Turkey
- Recruiting
- Tuba Yilmaz Bulut
-
Contact:
- TUBA YILMAZ BULUT, Dr.
- Phone Number: 05343435109
- Email: tuba_yilmaz1991@hotmail.com
-
-
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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Agreeing to participate in the study
- Having a complaint of urinary incontinence
- Being a woman between the ages of 45-55
- Being communicable
- Having a device (phone, tablet, computer) that can participate in online conversations
- Being in the premenopausal period
Exclusion Criteria:
- Women who do not complain of urinary incontinence
- Women in menopause
- Women who left unanswered questions on their scale forms
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental
Kegel exercises and Ba Duan Jin applications will be applied to women in the experimental group online (via Zoom application) in two sessions per week for a total of 8 weeks.
Afterwards, women will be asked to perform these practices three days a week for 12 weeks and will be monitored.
The research will last a total of 16 weeks.
|
Kegel exercises and Ba Duan Jin applications online
|
|
Active Comparator: Control
Women in the control group will be given training on Kegel exercises and Ba Duan Jin applications after the research is completed.
|
Behavioral: training on Kegel exercises and Ba Duan Jin applications after the research is completed
Women in the control group will be given training on Kegel exercises and Ba Duan Jin applications after the research is completed.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Psychological Well-Being Scale
Time Frame: 4 month
|
It was developed by Diener et al. to measure socio-psychological well-being as a complement to existing well-being measurements.
The adaptation of the scale into Turkish was carried out by Telef.
Factor loadings of the scale items were calculated between .54 and .76.
The Cronbach's alpha internal consistency coefficient obtained in the reliability study of the scale was calculated as .80.
All items are worded positively.
Scores range from 8 to 56.
|
4 month
|
|
Incontinence Quality of Life Scale
Time Frame: 4 month
|
It was developed by Wagner et al. in 1996 in America to determine the quality of life of patients with urinary incontinence.
However, the scale was revised by Patrick et al. in 1999, and during the creation of the European versions, six questions were removed and the number of questions was reduced to 22 by evaluating the psychometric measurements.
In our country, the validity and reliability of I-QOL was determined by Özerdoğan.
It is converted to a scale value up to 100.
Higher scores indicate a better level of quality of life than lower scores.
|
4 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: TUBA YILMAZ BULUT, Dr., Kocaeli University
- Study Chair: Aynur ATAMAN KUFACI, Lecturer, Sinop University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Wagner TH, Patrick DL, Bavendam TG, Martin ML, Buesching DP. Quality of life of persons with urinary incontinence: development of a new measure. Urology. 1996 Jan;47(1):67-71; discussion 71-2. doi: 10.1016/s0090-4295(99)80384-7.
- Telef BB. Psychological Well-Being Scale (PIOO): Adaptation to Turkish, Validity and Reliability Study. Hacettepe Faculty of Education Journal, 2013; 28(3):374-384
- Diener E, Wirtz D, Tov W, Kim-Prieto C, Choi D, Oishi S, Biswas-Diener R. New well-being measures: Short scales to assess flourishing and positive and negative feelings. Social Indicators Research, 2010; 97: 143-156.
- Özerdoğan N, Kızılkaya NB. Prevalence, risk factors, and impact on quality of life of urinary incontinence in women aged 20 and over in Eskişehir, Bilecik, Afyon, Kütahya provinces. Journal of Nursing 2003; 13:37-50.
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)
April 1, 2024
Primary Completion (Estimated)
July 1, 2024
Study Completion (Estimated)
March 1, 2025
Study Registration Dates
First Submitted
February 19, 2024
First Submitted That Met QC Criteria
February 29, 2024
First Posted (Actual)
March 1, 2024
Study Record Updates
Last Update Posted (Actual)
April 3, 2024
Last Update Submitted That Met QC Criteria
April 1, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Behavioral Symptoms
- Mental Disorders
- Metabolic Diseases
- Urologic Diseases
- Lower Urinary Tract Symptoms
- Urological Manifestations
- Infant, Newborn, Diseases
- Genetic Diseases, Inborn
- Urination Disorders
- Metabolism, Inborn Errors
- Lysosomal Storage Diseases
- Lipid Metabolism Disorders
- Elimination Disorders
- Lipidoses
- Lipid Metabolism, Inborn Errors
- Cholesterol Ester Storage Disease
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Urogenital Diseases
- Male Urogenital Diseases
- Urinary Incontinence
- Enuresis
- Wolman Disease
Other Study ID Numbers
- E-57428665-050.04-240046
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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