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

4. juni 2026 opdateret af: 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 (Haile et al., 2021). 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 (Leung et al., 2015). Ankle muscle performance of individuals with LBP during gait becomes more clinically important as it may provide insights into the mechanisms of ankle strategies (Claeys et al., 2015). 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 (Bonetti et al., 2018).

Studieoversigt

Status

Ikke rekrutterer endnu

Intervention / Behandling

Detaljeret beskrivelse

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.

Undersøgelsestype

Observationel

Tilmelding (Anslået)

50

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Undersøgelse Kontakt Backup

Studiesteder

    • Gharbia Governorate
      • Tanta, Gharbia Governorate, Egypten, 31511
        • Al-Salam University
        • Kontakt:
          • Ayman Mohammed Elmakakey, Associate Professor
          • Telefonnummer: +20403386400
          • E-mail: info@sue.edu.eg
        • Kontakt:
          • Aya Elkomy, Lecturer
          • Telefonnummer: +20 106 603 4330
          • E-mail: info@sue.edu.eg

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen

Tager imod sunde frivillige

Ingen

Prøveudtagningsmetode

Ikke-sandsynlighedsprøve

Studiebefolkning

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.

Beskrivelse

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

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

Kohorter og interventioner

Gruppe / kohorte
Intervention / Behandling
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

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Torque parameters for ankle Isokinetic testing of plantar flexors and dorsi flexors for dominant and non-dominant limbs.
Tidsramme: 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.
Tidsramme: 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.
Tidsramme: 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.
Tidsramme: 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)

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Level of pain intensity
Tidsramme: Baseline
Will be measured through Visual Analogue Scale (VAS)
Baseline
Level of functional disability
Tidsramme: Baseline
Will be assessed through Arabic version of Modified Oswestry Disability Index (MODI)
Baseline
Kinesiophobia and fearing of physical activity and work
Tidsramme: Baseline
Will be assessed through Fear Avoidance Beliefs Questionnaire (FABQ)
Baseline
Overall body fatiguability status and physical function
Tidsramme: Baseline
Will be assessed through Fatigue Severity Scale (FSS)
Baseline
Lumbo-sacral angle
Tidsramme: Baseline
Will be measured by Fergusson's method on Lateral X-ray films of lumbo-sacral region for each patient
Baseline
Assessment of core muscles endurance
Tidsramme: Baseline
Will be assessed through McGill endurance test
Baseline

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Studieleder: Maha Mostafa Alibeiny, Associate Professor, Cairo University
  • Studieleder: Hany Mohamed Hamed, Associate Professor, Faculty of Medicine, Kafrelsheikh University

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Generelle publikationer

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

7. juni 2026

Primær færdiggørelse (Anslået)

30. oktober 2026

Studieafslutning (Anslået)

1. december 2026

Datoer for studieregistrering

Først indsendt

4. juni 2026

Først indsendt, der opfyldte QC-kriterier

4. juni 2026

Først opslået (Faktiske)

9. juni 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

9. juni 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

4. juni 2026

Sidst verificeret

1. juni 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • Ankle Isokinetic in CNSLBP

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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Ingen

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Ingen

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Kliniske forsøg med Humac Isokinetic 2015 System 2

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