- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05339516
The Association Between Urinary Incontinence, Physical Performance, Physical Activity Levels in Women With Low Back Pain
The Association Between Urinary Incontinence, Physical Performance and Physical Activity Level in Women With Low Back Pain a Cross-Sectional Study
Study Overview
Status
Conditions
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Pinar Yasar, MSc
- Phone Number: +905350145340
- Email: pinarergoz@gmail.com
Study Locations
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Isparta, Turkey, 32100
- Recruiting
- Faculty of Health Sciences
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Contact:
- Pınar Yasar, MSc
- Phone Number: +905350145340
- Email: pinarergoz@gmail.com
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria For Healthy Group:
- 30-65 years women
- Agreeing to involve in the study
Inclusion Criteria For Women With Low Back Pain Group:
- 30-65 years women
- Having low back pain for at least 3 months
- Scoring pain at least 1 in Visual Analog Scale(VAS)
- Agreeing to involve in the study
Exclusion Criteria:
- Any kind of surgery history in low back area
- Surgery history in lower limbs
- Acute low back pain
- Having a neurological disease
- Having sensory deficists
- The ones with rheumatological diseases which can cause low back pain
- Being pregnant
- Having a disc hernia pressuring to sacral nerves
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
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Healthy group
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Women with low back pain
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Visual Analog Scale(VAS)
Time Frame: Baseline
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Visual Analogue Scale (VAS) will be used to evaluate the severity of low back pain.
The back pain they feel during activity and rest will be questioned separately from the participants.
For this assessment, patients will be asked to mark their pain intensity on a 10-centimeter line.
Pain intensity will be determined by measuring the distance of the marked point to the "0" point with a tape measure.
Scoring is made between 0-10 and "0 means no pain"- "10 means the most severe pain imaginable".
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Baseline
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International Consultation on Incontinence Questionnaire-Short Form (ICIQ-SF)
Time Frame: Baseline
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The six-question form allows evaluation of the frequency of urinary incontinence and during which activities it occurs.
The validity and reliability study of the Turkish version of the test was done by Çetinel et al. made by Scoring is done with frequency, amount and degree of impact questions, a total score between 0-21 is obtained.
A low score indicates that urinary incontinence affects the quality of life less, and a high score indicates that the involvement is high.
For the ICIQ-SF, a score of 8 and above was determined as the most appropriate cut-off value for irritating urine leakage.
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Baseline
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International Physical Activity Questionnaire(IPAQ)
Time Frame: Baseline
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The physical activity level of the participants will be evaluated with the International Physical Activity Questionnaire (IPAQ).
The survey consists of a total of 5 sections and 27 questions.
Information is obtained about the light, moderate and vigorous activities that the person has done in the last week and the sitting time.
For physical activities performed for at least 10 minutes, the MET value (metabolic equivalent) is multiplied by the number of days and minutes to obtain the MET-min/week score.
Classification according to the energy level spent in METs is made as no physical activity (MET=<600), insufficient activity (MET=600-3000), and adequate activity level (MET= >3000).
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Baseline
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Muscle Strength Testing
Time Frame: Baseline
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The muscle strength of the participants will be determined by the Manual Muscle Test.
The person is asked to move against gravity by taking the appropriate position for the muscle to be evaluated.
If the movement can be done up to the desired part (3) it is scored as medium, if it receives minimal resistance (3+) if it gets a little good from the middle, if it can get moderate resistance (4) good, if it can get full resistance (5) it is normal.
Muscle strength of the shoulder and elbow flexors in the upper extremity and hip flexors in the lower extremities will be evaluated.
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Baseline
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Endurance Testing
Time Frame: Baseline
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Trunk Flexor Endurance test and Wall-Sit-Hold Test will be used to evaluate trunk and lower extremity endurance. Wall-Sit- Hold Test: The participant leans his back against the wall, spreads his feet shoulder-width apart and squats by bringing his knees to 90 degrees of flexion. The time during which the position can be held is recorded |
Baseline
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Agility Testing
Time Frame: Baseline
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Burpee Agility Test will be used for the agility evaluation of the participants.
The test consists of 4 stages.
Initially, the standing participant moves into a half-squat position, then into a stance on the floor with hands and feet close together.
Then the participant takes the plank position with the arms fully extended by throwing his legs back and then returning to the previous position.
He then stands up and returns to the starting position and claps his hands above his head once.
The standard test duration is 3 minutes, but a modified version of 1 minute will be used in order to be applicable to individuals with low physical activity.
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Baseline
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Flexibility Testing
Time Frame: Baseline
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Flexibility will be assessed with the sit and reach test.
The person sits in a long sitting position with his legs straight, the soles of the feet are in contact with the 31 cm high evaluation table.
The participant is then asked to reach forward as far as he can, keeping his knees straight, with one hand on the other.
Starting position and the farthest point that the middle finger can reach at the end of the movement is measured and the difference is recorded.
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Baseline
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
- 72867572-050.01.04-
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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