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The Association Between Urinary Incontinence, Physical Performance, Physical Activity Levels in Women With Low Back Pain

14 de abril de 2022 atualizado 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.

Visão geral do estudo

Status

Recrutamento

Condições

Tipo de estudo

Observacional

Inscrição (Antecipado)

146

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Nome: Pinar Yasar, MSc
Número de telefone: +905350145340
E-mail: pinarergoz@gmail.com

Locais de estudo

Peru
- - Isparta, Peru, 32100
    - Recrutamento
    - Faculty of Health Sciences
    - Contato:
      
      Pınar Yasar, MSc
      
      Número de telefone: +905350145340
      
      E-mail: pinarergoz@gmail.com

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

26 anos a 61 anos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Fêmea

Método de amostragem

Amostra Não Probabilística

População do estudo

30-65 ages women who live in city of Isparta in Turkey.

Descrição

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

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

Modelos de observação: Coorte
Perspectivas de Tempo: Transversal

Número de grupos/coortes

Coortes e Intervenções

Grupo / Coorte
Grupo saudável
Women with low back pain

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado	Descrição da medida	Prazo
Visual Analog Scale(VAS) Prazo: Baseline	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".	Baseline
International Consultation on Incontinence Questionnaire-Short Form (ICIQ-SF) Prazo: Baseline	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.	Baseline
International Physical Activity Questionnaire(IPAQ) Prazo: Baseline	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).	Baseline
Muscle Strength Testing Prazo: Baseline	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.	Baseline
Endurance Testing Prazo: Baseline	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
Agility Testing Prazo: Baseline	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.	Baseline
Flexibility Testing Prazo: Baseline	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.	Baseline

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Pinar Yasar

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

29 de novembro de 2021

Conclusão Primária (Antecipado)

1 de abril de 2022

Conclusão do estudo (Antecipado)

1 de maio de 2022

Datas de inscrição no estudo

Enviado pela primeira vez

8 de abril de 2022

Enviado pela primeira vez que atendeu aos critérios de CQ

14 de abril de 2022

Primeira postagem (Real)

21 de abril de 2022

Atualizações de registro de estudo

Última Atualização Postada (Real)