Deze pagina is automatisch vertaald en de nauwkeurigheid van de vertaling kan niet worden gegarandeerd. Raadpleeg de Engelse versie voor een brontekst.

Core Endurance Versus Segmental Stabilization Exercise in Recreational Athletes With Low Back Pain

17 augustus 2026 bijgewerkt door: Doç.Dr.Ömer Şevgin, Uskudar University

Comparison of the Effects of Core Endurance Exercises and Segmental Stabilization Exercises on Low Back Pain and Core Endurance in Recreational Athletes With Non-Specific Low Back Pain: A Randomized Trial

Low back pain is a common musculoskeletal complaint among athletes, and most cases are classified as non-specific low back pain, in which no clear anatomical or pathological source of pain can be identified. Recreational athletes, who exercise regularly for health and fitness rather than for competition, often have less structured training planning and technical supervision than professional athletes, which may increase their susceptibility to musculoskeletal complaints. Core stability has become an important consideration in the prevention and management of low back pain. The core region includes the abdominal muscles, paraspinal muscles, diaphragm, and pelvic floor muscles, and plays an important role in maintaining spinal stability. Reduced activation and endurance of these muscles may increase the load on the lumbar spine and contribute to the development of low back pain. This randomized trial compares two exercise approaches in recreational athletes with non-specific low back pain: a core endurance exercise program and a segmental stabilization exercise program targeting the transversus abdominis and lumbar multifidus. Participants are randomly assigned to one of the two programs, both delivered three days per week for six weeks under physiotherapist supervision. Pain and functional status, dynamic balance, and core muscle endurance are assessed before the program and at the end of the six-week program.

Studie Overzicht

Gedetailleerde beschrijving

Design and setting This is a two-arm, parallel-group randomized trial conducted at a sports club facility.

Institutional permission for the study site has been obtained. Participants Recreational athletes who have recently begun regular physical activity and who report non-specific low back pain are enrolled. Participants provide written informed consent after receiving detailed information about the purpose of the study, the tests to be performed, and the exercise protocol. Sampling and randomization Convenience sampling is used to identify eligible participants, followed by simple random allocation to one of the two exercise groups: the core endurance exercise group or the segmental stabilization exercise group. Allocation is 1:1. Interventions Both exercise programs are delivered three days per week for six weeks. Segmental stabilization group: exercises target the transversus abdominis and lumbar multifidus and comprise stabilization exercises in the quadruped position, transversus abdominis activation exercises in the supine position with the knees flexed, lumbar multifidus activation exercises in the prone position, and standing postural control exercises involving co-activation of the transversus abdominis and lumbar multifidus.

Core endurance group: exercises are performed under the supervision of a certified physiotherapist and comprise the front plank, the side plank, and the superman plank.

Each exercise consists of 20 repetitions with a 15-second isometric hold per repetition.

The set is repeated twice, with a 3-minute rest between sets. In the front plank the participant is supported on the forearms and toes, with the shoulders aligned over the elbows and the trunk and lower limbs maintained in a straight line, producing simultaneous activation of the abdominal and paraspinal muscles. In the side plank the participant is supported on one forearm with the body held in a straight line, the shoulder aligned with the elbow and the pelvis lifted from the floor, targeting the oblique muscles. In the superman plank the participant lies prone with the arms extended overhead and simultaneously lifts the upper and lower limbs from the floor, producing trunk extension and targeting the lumbar extensor muscles. Outcome assessment Assessments are performed at baseline (week 0) and at the end of the six-week program (week 6). Demographic information including age, sex, and sports history is recorded.

Functional status and pain are assessed with the Micheli Functional Scale, dynamic balance with the Star Excursion Balance Test, and core muscle endurance with clinical endurance tests. Variables The independent variable is the type of exercise program (core endurance exercises versus segmental stabilization exercises). The dependent variables are pain level, core muscle endurance, and dynamic balance performance. Statistical analysis Normality of distribution is assessed with histogram curves and the Shapiro-Wilk test, and homogeneity of variance with the Levene test. Parametric or non-parametric tests are selected accordingly. Analyses are performed with IBM SPSS Statistics 20. Independent samples t-tests are used to compare demographic characteristics between groups. Multivariate analysis of variance is used to evaluate between-group and within-group changes, with time (baseline and post-intervention measurements) as the within-subject factor and group as the between-subject factor. Where a statistically significant difference is found, post-hoc analyses are performed with the Tukey test. Change scores between groups are also compared with independent samples t-tests.

Studietype

Ingrijpend

Inschrijving (Geschat)

60

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Locaties

      • Istanbul, Turkije (Türkiye)
        • Werving
        • Fitness club gym
        • Contact:
          • Armita Chitsaz
          • Telefoonnummer: +905456052365

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen

Accepteert gezonde vrijwilligers

Nee

Beschrijving

Inclusion Criteria:

  • Aged 18 years or older
  • Recreational athlete who has recently begun regular physical activity
  • Diagnosis of non-specific low back pain confirmed by an orthopaedic specialist
  • Two or more episodes of low back pain within the past year
  • Not participating in any other treatment program during the study period

Exclusion Criteria:

  • Radicular (nerve root) signs
  • Underlying systemic or visceral disease
  • Diagnosis of ankylosing spondylitis
  • Spinal pathology such as spondylolysis or spondylolisthesis
  • Previous lumbar spine surgery
  • History of vestibular dysfunction
  • Lower extremity injury within the past month
  • History of traumatic concussion within the past three months

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Enkel

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Core endurance exercise
Participants perform a core endurance exercise program consisting of the front plank, the side plank, and the superman plank, three days per week for six weeks under physiotherapist supervision. Each exercise consists of 20 repetitions with a 15-second isometric hold, repeated for two sets with a 3-minute rest between sets.

Supervised isometric core endurance training comprising the front plank, side plank, and superman plank.

Each exercise: 20 repetitions of a 15-second isometric hold, two sets, 3-minute rest between sets. Three sessions per week for six weeks.

Supervised motor-control training targeting the transversus abdominis and lumbar multifidus, comprising quadruped stabilization, supine transversus abdominis activation with knees flexed, prone lumbar multifidus activation, and standing postural control with co-activation of both muscles. Three sessions per week for six weeks.
Actieve vergelijker: Segmental stabilization exercise
Participants perform a segmental stabilization exercise program targeting the transversus abdominis and lumbar multifidus, three days per week for six weeks under physiotherapist supervision. The program comprises quadruped stabilization exercises, supine transversus abdominis activation with the knees flexed, prone lumbar multifidus activation, and standing postural control exercises involving co-activation of both muscles.

Supervised isometric core endurance training comprising the front plank, side plank, and superman plank.

Each exercise: 20 repetitions of a 15-second isometric hold, two sets, 3-minute rest between sets. Three sessions per week for six weeks.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change in low back pain and functional status (Micheli Functional Scale)
Tijdsspanne: Baseline (week 0) and at the end of the six-week exercise program (week 6)
The Micheli Functional Scale is a five-item scale developed to assess low back pain related functional impairment and pain related changes in performance in athletes. It comprises one symptom question, three activity questions (extension, flexion, and jumping), and a visual analogue scale section. The symptom question is scored from 0 to 5; the activity questions are scored from 0 to 4 for extension, from 0 to 3 for flexion, and from 0 to 3 for jumping. The visual analogue scale section provides a 10-point assessment on a 10 cm line. The total score is calculated out of 25 and multiplied by 4 to produce a standardized score from 0 to 100. Lower scores indicate better functional status and higher scores indicate greater functional impairment.
Baseline (week 0) and at the end of the six-week exercise program (week 6)

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Studie stoel: Armita Chitsaz, Uskudar University

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

15 augustus 2026

Primaire voltooiing (Geschat)

1 december 2026

Studie voltooiing (Geschat)

30 december 2026

Studieregistratiedata

Eerst ingediend

7 augustus 2026

Eerst ingediend dat voldeed aan de QC-criteria

7 augustus 2026

Eerst geplaatst (Werkelijk)

12 augustus 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

18 augustus 2026

Laatste update ingediend die voldeed aan QC-criteria

17 augustus 2026

Laatst geverifieerd

1 augustus 2026

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • Uskudar27
  • Uskudar University (Andere identificatie: Non-Interventional Research Ethics Committee)

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Beschrijving IPD-plan

Individual participant data will not be made publicly available. De-identified data supporting the findings may be made available from the corresponding author on reasonable request, subject to institutional approval.

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

Abonneren