The Association Between Urinary Incontinence, Physical Performance, Physical Activity Levels in Women With Low Back Pain
14 de abril de 2022 actualizado por: Pinar Yasar
The Association Between Urinary Incontinence, Physical Performance and Physical Activity Level in Women With Low Back Pain a Cross-Sectional Study
The study is searching for the correlation between low back pain(LBP), physical performance, urinary incontinence and physical activity levels in women.
Lower physical performance, more frequent urinary incontinence and less physical activity are expected in women who have LBP.
Descripción general del estudio
Estado
Reclutamiento
Condiciones
Tipo de estudio
De observación
Inscripción (Anticipado)
146
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Estudio Contacto
- Nombre: Pinar Yasar, MSc
- Número de teléfono: +905350145340
- Correo electrónico: pinarergoz@gmail.com
Ubicaciones de estudio
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Isparta, Pavo, 32100
- Reclutamiento
- Faculty of Health Sciences
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Contacto:
- Pınar Yasar, MSc
- Número de teléfono: +905350145340
- Correo electrónico: pinarergoz@gmail.com
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Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
26 años a 61 años (Adulto, Adulto Mayor)
Acepta Voluntarios Saludables
No
Géneros elegibles para el estudio
Femenino
Método de muestreo
Muestra no probabilística
Población de estudio
30-65 ages women who live in city of Isparta in Turkey.
Descripción
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
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Modelos observacionales: Grupo
- Perspectivas temporales: Transversal
Cohortes e Intervenciones
Grupo / Cohorte |
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Grupo saludable
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Women with low back pain
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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Visual Analog Scale(VAS)
Periodo de tiempo: 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)
Periodo de tiempo: 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)
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Actual)
29 de noviembre de 2021
Finalización primaria (Anticipado)
1 de abril de 2022
Finalización del estudio (Anticipado)
1 de mayo de 2022
Fechas de registro del estudio
Enviado por primera vez
8 de abril de 2022
Primero enviado que cumplió con los criterios de control de calidad
14 de abril de 2022
Publicado por primera vez (Actual)
21 de abril de 2022
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
21 de abril de 2022
Última actualización enviada que cumplió con los criterios de control de calidad
14 de abril de 2022
Última verificación
1 de abril de 2022
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 72867572-050.01.04-
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
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