The Association Between Urinary Incontinence, Physical Performance, Physical Activity Levels in Women With Low Back Pain
2022年4月14日 更新者: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.
調査の概要
研究の種類
観察的
入学 (予想される)
146
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究連絡先
- 名前:Pinar Yasar, MSc
- 電話番号:+905350145340
- メール:pinarergoz@gmail.com
研究場所
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Isparta、七面鳥、32100
- 募集
- Faculty of Health Sciences
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コンタクト:
- Pınar Yasar, MSc
- 電話番号:+905350145340
- メール:pinarergoz@gmail.com
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参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
26年~61年 (大人、高齢者)
健康ボランティアの受け入れ
いいえ
受講資格のある性別
女性
サンプリング方法
非確率サンプル
調査対象母集団
30-65 ages women who live in city of Isparta in Turkey.
説明
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
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか?
デザインの詳細
- 観測モデル:コホート
- 時間の展望:断面図
コホートと介入
グループ/コホート |
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健康グループ
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Women with low back pain
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
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Visual Analog Scale(VAS)
時間枠: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)
時間枠: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)
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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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協力者と研究者
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スポンサー
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (実際)
2021年11月29日
一次修了 (予想される)
2022年4月1日
研究の完了 (予想される)
2022年5月1日
試験登録日
最初に提出
2022年4月8日
QC基準を満たした最初の提出物
2022年4月14日
最初の投稿 (実際)
2022年4月21日
学習記録の更新
投稿された最後の更新 (実際)
2022年4月21日
QC基準を満たした最後の更新が送信されました
2022年4月14日
最終確認日
2022年4月1日
詳しくは
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