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Isokinetic Profile of Ankle Joint Muscles in Chronic Non Specific Low Back Pain Patients

2026年7月15日 更新者:Mohamed Hazem Abdelhakam Elshafey、Cairo University

The Relationship Between Chronic Non-Specific Low Back Pain and Isokinetic Performance of Ankle Joint Muscles

Chronic non-specific low back pain and its resulting infirmity have become a huge health and socioeconomic burden. Low back pain is reportedly associated with decreased activities of daily living and quality of life. Previous literature supports the presence of a link between CLBP and lower limb kinematics that can contribute to functional limitations and disability. For example, CLBP commonly coexist with postural and structural asymmetry. Ankle muscle performance of individuals with LBP during gait becomes more clinically important as it may provide insights into the mechanisms of ankle strategies. The isokinetic testing is an assessment method of high effectivity and trustworthiness that can be used to compare bilateral and agonist/ antagonist ankle muscles strength of normal subjects and athletes. It can be used to analyze muscular performance and differences in muscle performance between dominant and non-dominant limbs.

調査の概要

詳細な説明

This study will involve 50 male patients diagnosed with CNSLBP and will correlate between level of pain, disability, psychological status, and overall body fatiguability, core muscles endurance with the strength, endurance, joint angle position, and time parameters of isokinetic testing profile of ankle joint.

研究の種類

観察的

入学 (推定)

50

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

研究連絡先のバックアップ

研究場所

    • Gharbia Governorate
      • Tanta、Gharbia Governorate、エジプト、31511
        • 募集
        • Al-Salam University
        • コンタクト:
          • Ayman Mohammed Elmakakey, Associate Professor
          • 電話番号:+20403386400
          • メール:info@sue.edu.eg
        • コンタクト:
          • Aya Elkomy, Lecturer
          • 電話番号:+20 106 603 4330
          • メール:info@sue.edu.eg

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

  • 大人

健康ボランティアの受け入れ

いいえ

サンプリング方法

非確率サンプル

調査対象母集団

50 male patients aged 20-40 years, diagnosed with CNSLBP through direct referral from their orthopedic surgeon after excluding the previous criteria.

Medical assessment for recruiting, diagnosis, and including or excluding will be done at Kafrelsheikh University Hospitals.

説明

Inclusion Criteria:

  1. 50 male patients diagnosed with Chronic non-specific low back pain through direct referral from their orthopedic surgeon.
  2. Each patient will be diagnosed by "Waddle sign"
  3. Age limit 20-40 years.
  4. BMI: less than 30.
  5. Pain duration: chronic more than 3 months or 12 weeks.
  6. Pain location: Between T12- and lower gluteal folds.
  7. Pain Intensity: At least have 3 out of 10 on VAS.
  8. Level of functional disability: 21%-40% on MODI.
  9. Each patient sign an informed consent.

Exclusion Criteria:

  1. Unexplained weight loss.
  2. History of malignancy.
  3. Recent trauma within last 12 months.
  4. Osteoporosis.
  5. Cauda Equina Symptoms.
  6. Herniated discs.
  7. Radicular signs.
  8. Spine fractures.
  9. Spinal Canal Stenosis.
  10. Myofascial Pain Syndrome.
  11. Spondylolisthesis.
  12. Rheumatological history.
  13. CVS manifestations.
  14. GIT manifestations.
  15. Psychiatric disorders.
  16. Weakness or parathesis in L.L.
  17. History of back surgery.
  18. Chronic Ankle Instability.
  19. Scoliosis or leg length discrepancies.
  20. Neurological and systemic manifestations such Epilepsy, muscular diseases, or seziures.
  21. Mechanical back pain

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

コホートと介入

グループ/コホート
介入・治療
Study Group
50 patient diagnosed with Chronic non-specific low back pain will be evaluated and assessed by humac isokinetic for ankle profile, Mcgill core endurance tests, level of pain, disability, fatiguability through questionnaires and measuring Lumbosacral angle for each patient, and correlate all variables with each others.
Humac isokinetic device will be used for testing and assessing ankle joint profile including torque, endurance, joint position, and time parameters for both limbs for 50 patients diagnosed with chronic non specific low back pain

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
Torque parameters for ankle Isokinetic testing of plantar flexors and dorsi flexors for dominant and non-dominant limbs.
時間枠:Baseline (Single assessment session per patient)
Ankle torque parameters will be tested at velocity of 30°/s, these parameters will include (peak torque - peak torque / BW - Cof of Variance)
Baseline (Single assessment session per patient)
Endurance and power parameters for ankle Isokinetic testing of plantar flexors and dorsi flexors for dominant and non-dominant limbs.
時間枠:Baseline (single assessment session per patient)
Ankle torque parameters will be tested at velocity of 180°/s, these parameters will include (fatigue index - Total work - Average Power/reps)
Baseline (single assessment session per patient)
Position parameters for ankle Isokinetic testing of plantar flexors and dorsi flexors for dominant and non-dominant limbs.
時間枠:Baseline (Single assessment session per patient)
Position torque parameters will be tested at two velocities of 30°/s, and 180°/s these parameters will include (Joint angle at peak torque - Range of motion)
Baseline (Single assessment session per patient)
Time parameters for ankle Isokinetic testing of plantar flexors and dorsi flexors for dominant and non-dominant limbs.
時間枠:Baseline (Single assessment session per patient)
Time torque parameters will be tested at two velocities of 30°/s, and 180°/s these parameters will include (Time to peak torque - Force decay time - Delay time)
Baseline (Single assessment session per patient)

二次結果の測定

結果測定
メジャーの説明
時間枠
Lumbo-sacral angle
時間枠:Baseline
Will be measured by Fergusson's method on Lateral X-ray films of lumbo-sacral region for each patient
Baseline
Level of pain intensity
時間枠:Baseline
Will be measured through Visual Analogue Scale (VAS) VAS is a proven, evaluative tool for measuring both acute and chronic pain as scores is recorded by placing a handwriting mark along a 10-cm line that represents a pain spectrum between "no pain" and "worst pain" as the word descriptions "no pain" on the left and "worst imaginable pain" on the right serve as anchors for the 100-mm long horizontal line.
Baseline
Level of functional disability
時間枠:Baseline

Will be assessed through Arabic version of Modified Oswestry Disability Index (MODI).

The Oswestry Low Back Pain Disability Index is a 10-item self-assessment questionnaire with 6 levels of answers ranging from 0 to 5. Pain, personal care, lifting and moving objects, walking, sitting, standing, sleep disorders caused by LBP, sex life, social life, and traveling are among these items. A total score is computed, and the percentage of disability (score obtained divided by 50 and multiplied by 100) ranges from 0% (no disability) to 100% (complete disability) (complete disability). The following scores are used to interpret this scale: 0 to 20%: minimal disability; 20 to 40%: moderate disability; 40 to 60%: severe disability; 60 to 80%: crippling low back pain; and above 80%: the person is confined to bed. To obtain the score, the sum of the scores is divided by the total possible score (i.e., 50). To obtain the percentage of a patient's disability, the resulting total is multiplied by 100

Baseline
Kinesiophobia and fearing of physical activity and work
時間枠:Baseline
Will be assessed through Fear Avoidance Beliefs Questionnaire (FABQ) The questionnaire consists of 16 items in which a patient rates their agreement with each statement on a 7-point Likert scale. Where 0= completely disagree, 6=completely agree. There is a maximum score of 96. A higher score indicates more strongly held fear avoidance beliefs. There are two subscales within the FABQ; the work subscale (FABQw) with 7 questions (maximum score of 42) and the physical activity subscale (FABQpa) with 4 questions (maximum score of 24). The numbers in parentheses below designate which items from the FABQ are included in each subscale. The questionnaire takes approximately 10 minutes to complete. The higher the score, the higher the subject's fear-avoidance beliefs
Baseline
Overall body fatiguability status and physical function
時間枠:Baseline
Will be assessed through Fatigue Severity Scale (FSS) Arabic version of the FSS is a 9-item scale which measures the severity of fatigue and its effect on a person's activities. Answers are scored on a seven- point scale where 1 = strongly disagree and 7 = strongly agree. This means the minimum score possible is nine and the highest is 63. The higher the score, the more severe the fatigue is and the more it affects the person's activities.
Baseline
Assessment of core muscles endurance
時間枠:Baseline
Will be assessed through McGill endurance test For the McGill test, the participant back leaned against a jig in a sit-up position that will be 60 degrees (degrees) off the ground, their knees bent 90 degrees, their hips folded over their chests, their hands on the shoulder across from them, and their feet fastened. The patient will be instructed to maintain isometric posture for the longest period of time feasible before the researcher pushed the jig back 10 centimeters. Thus, when the patients' backs touched the jig, it was considered a failure. The researcher also will note how long the subjects maintained an isometric stance, which is typically between one and two minutes.
Baseline
Core endurance The Sorenson test
時間枠:Baseline
The Sorenson test will be carried out with the individuals' upper bodies off the end of the test bench and their pelvises, knees, and hips restrained. Hands were placed on opposite shoulders while the subjects' upper bodies were held across their chests. Failure is defined as the moment that a subject's upper body deviated from the horizontal position, and the researcher will note the amount of time that a subject typically maintained a straight posture for between one and two minutes.
Baseline
Core endurance Side Plank test
時間枠:Baseline
Side plank test will be conducted with subjects lied on side, then researcher will ask to lift body on elbow, forearm, and feet will be stacked to create a straight line from head to toes. Thus, failure will be determined when subjects' body would be dropped; and researcher will record time that subjects has hold body straight with normal range of one and two minutes.
Baseline

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • スタディディレクター:Maha Mostafa Alibeiny, Associate Professor、Cairo University
  • スタディディレクター:Hany Mohamed Hamed, Associate Professor、Faculty of Medicine, Kafrelsheikh University

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

一般刊行物

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)

2026年6月13日

一次修了 (推定)

2026年10月30日

研究の完了 (推定)

2026年12月1日

試験登録日

最初に提出

2026年6月4日

QC基準を満たした最初の提出物

2026年6月4日

最初の投稿 (実際)

2026年6月9日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月17日

QC基準を満たした最後の更新が送信されました

2026年7月15日

最終確認日

2026年7月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • Ankle Isokinetic in CNSLBP

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個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

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いいえ

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いいえ

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