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Core Stabilization and Kinesthetic Training in Diplegic CP

28 aprile 2026 aggiornato da: Nabisha Yaseen, University of Lahore

Comparative Effects of Core Stabilization Exercises and Kinesthetic Training in Diplegic Cerebral Palsy

This randomized controlled trial aimed to compare the effects of core stabilization exercises (CSE) and kinesthetic training (KT) on postural control in children with spastic diplegic cerebral palsy (GMFCS Level III), aged 4-8 years. Cerebral palsy was recognized as a non-progressive neurological disorder that affects movement, posture, and motor function, often leading to impaired balance, reduced trunk control, and decreased functional independence. Postural instability was identified as a key concern in diplegic CP, and effective rehabilitation strategies were considered essential to improve mobility and daily functioning. Core stabilization exercises focused on strengthening deep trunk muscles to enhance stability and alignment, whereas kinesthetic training emphasized proprioceptive awareness and neuromuscular coordination to improve movement accuracy and balance. Although both interventions had shown benefits individually, their comparative effectiveness remained unclear.

A total of 32 participants were recruited using purposive sampling and were randomly assigned into two groups: CSE (n=16) and KT (n=16). Both groups received conventional physiotherapy for 15 minutes followed by 30 minutes of their respective interventions, three times per week for 12 weeks. Outcome assessment was conducted at baseline, mid-intervention (6 weeks), and post-intervention (12 weeks) using the Pediatric Berg Balance Scale (PBBS) to evaluate static and dynamic balance. Data were analyzed using SPSS, applying paired t-tests for within-group comparisons and independent t-tests for between-group analysis, with significance set at p < 0.05. This study aimed to determine the more effective intervention for improving balance and functional outcomes, thereby supporting evidence-based clinical practice in pediatric rehabilitation.

A total of 32 participants will be recruited using purposive sampling and randomly assigned into two groups: CSE (n=16) and KT (n=16). Both groups will receive conventional physiotherapy for 15 minutes followed by 30 minutes of their respective interventions, three times per week for 12 weeks. Outcome assessment will be conducted at baseline, mid-intervention (6 weeks), and post-intervention (12 weeks) using the Pediatric Berg Balance Scale (PBBS) to evaluate static and dynamic balance. Data will be analyzed using SPSS, applying paired t-tests for within-group comparisons and independent t-tests for between-group analysis, with significance set at p < 0.05. This study aims to determine the more effective intervention for improving balance and functional outcomes, thereby supporting evidence-based clinical practice in pediatric rehabilitation.

Panoramica dello studio

Descrizione dettagliata

This randomized controlled trial was conducted to compare the effects of core stabilization exercises (CSE) and kinesthetic training (KT) on postural control in children diagnosed with spastic diplegic cerebral palsy classified at Gross Motor Function Classification System (GMFCS) Level III, aged between 4 and 8 years. Children within this classification typically demonstrated limitations in independent mobility and required assistive devices for ambulation, with notable impairments in trunk control and balance.

Postural instability in this population was identified as a major contributor to functional limitations, affecting activities such as sitting, standing, and transitional movements. Impaired trunk stability and reduced proprioceptive input were considered key factors influencing balance deficits. Therefore, targeted interventions focusing on trunk control and sensory-motor integration were explored to enhance postural regulation and functional independence.

Core stabilization exercises were implemented with the aim of improving activation, strength, and endurance of deep trunk musculature, including the transversus abdominis, multifidus, and pelvic stabilizers. These exercises emphasized controlled movements, alignment, and postural symmetry in various positions such as supine, sitting, and supported standing. Progression was based on the child's ability to maintain stability with reduced external support.

Kinesthetic training was designed to enhance proprioceptive awareness, joint position sense, and neuromuscular coordination. Activities included weight-shifting, balance challenges on stable and unstable surfaces, guided movement tasks, and functional reaching exercises. The intervention focused on improving the child's ability to perceive and adjust body position in space, thereby facilitating better motor control and balance responses.

Participants were recruited through purposive sampling from pediatric rehabilitation settings and were randomly allocated into two intervention groups using a simple randomization method. Each group consisted of 16 participants. Both groups received a standardized conventional physiotherapy program to ensure consistency in baseline care. This included stretching of spastic muscle groups, range-of-motion exercises, and facilitation of functional movements.

Following conventional therapy, participants underwent their assigned intervention (CSE or KT) for 30 minutes per session. The intervention was delivered three times per week over a period of 12 weeks. Sessions were supervised by trained physiotherapists to ensure adherence, safety, and appropriate progression of exercises.

Outcome measures were recorded at three time points: baseline (prior to intervention), mid-intervention (6 weeks), and post-intervention (12 weeks). Postural control and balance were assessed using the Pediatric Berg Balance Scale (PBBS), a validated tool for measuring both static and dynamic balance in pediatric populations. The scale included functional tasks such as sitting, standing, reaching, turning, and transferring, with scores reflecting the child's level of independence and stability.

Data were analyzed using statistical software. Within-group comparisons were performed to assess changes over time, while between-group comparisons were conducted to determine differences in effectiveness between the two interventions. Statistical significance was set at p < 0.05.

The findings of this study were intended to provide evidence regarding the relative effectiveness of core stabilization versus kinesthetic training in improving balance in children with spastic diplegic cerebral palsy. The results were expected to contribute to clinical decision-making and support the development of targeted rehabilitation protocols aimed at enhancing functional outcomes and quality of life in this population.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

32

Fase

  • Non applicabile

Contatti e Sedi

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Luoghi di studio

    • Punjab Province
      • Lahore, Punjab Province, Pakistan, 42000
        • Sehat Medical Complex, Pediatric Rehabilitation Department, ULTH.

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  • Spastic diplegic CP
  • GMFCS Level III
  • Age range: 4 to 8 years
  • Must have verbal communication
  • Ability to follow verbal commands

Exclusion Criteria:

  • Severe cognitive impairment
  • History of epilepsy or seizures in the past 3 months.
  • Children with progressive neurological or genetic disorders (e.g., muscular dystrophy).
  • Any acute respiratory infection or chronic pulmonary disease
  • Any visual or auditory impairments

Piano di studio

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Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Core Stabilization Group
Participants in this group received a core stabilization exercise program focusing on deep abdominal and back muscles. The protocol included the plank, bird-dog, and dead bug exercises, which were performed three times per week for four weeks.
A 4-week exercise program focusing on deep abdominal and back muscles. Sessions are 45 minutes each, 3 times per week. Exercises include The Plank (front and side), Bird-Dog, and Dead Bug. Progression will be managed by increasing hold times and repetitions as the patient's stability improves.
Sperimentale: Kinesthetic Training Group
Participants in this group underwent kinesthetic training aimed at improving proprioception and joint position sense. This included weight-shifting and balance activities on stable and unstable surfaces, which were performed three times per week for four weeks.
A 4-week sensory-motor training program designed to improve proprioception and balance. Sessions are 45 minutes each, 3 times per week. Activities include single-limb standing, weight shifting on stable and unstable surfaces (like foam pads), and coordinated limb movements to enhance joint position sense and postural control.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Balance Control is measured using the PBBS to evaluate both static and dynamic postural stability.
Lasso di tempo: 6 months
The Pediatric Berg Balance Scale (PBBS) is a standardized clinical assessment used to measure functional balance and postural control in children with motor challenges. It consists of 14 distinct tasks that mimic activities of daily living, including the ability to sit and stand without support, transfer between chairs, reach forward, and pick up objects from the floor. Each task is evaluated on a 5-point scale ranging from 0 to 4, where a higher score reflects a greater level of independence and stability. With a maximum total score of 56, the PBBS serves as a reliable tool for tracking a child's progress over time and determining the effectiveness of therapeutic interventions. In this clinical trial, the scale is utilized at baseline, week 6, and week 12 to provide a clear quantitative record of the participant's balance improvements.
6 months

Collaboratori e investigatori

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Pubblicazioni e link utili

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Pubblicazioni generali

  • Eliasson, A. C., Krumlinde-Sundholm, L., Rösblad, B., Beckung, E., Arner, M., Ohrvall, A. M., & Rosenbaum, P. (2006). The Manual Ability Classification System (MACS) for children with cerebral palsy: scale development and evidence of validity and reliability. Dev Med Child Neurol, 48(7), 549-554.
  • Akay, T., & Murray, A. J. (2021). Relative contribution of proprioceptive and vestibular sensory systems to locomotion: opportunities for discovery in the age of molecular science. International Journal of Molecular Sciences, 22(3), 1467.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

8 agosto 2025

Completamento primario (Effettivo)

9 marzo 2026

Completamento dello studio (Effettivo)

10 aprile 2026

Date di iscrizione allo studio

Primo inviato

28 aprile 2026

Primo inviato che soddisfa i criteri di controllo qualità

28 aprile 2026

Primo Inserito (Effettivo)

6 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

6 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

28 aprile 2026

Ultimo verificato

1 aprile 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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