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Sprinter vs Skater Coordination Synergy Training for Balance and Coordination in Chronic Stroke (SPRINT-SKATE)

15 giugno 2026 aggiornato da: Dr Aqsa Saman, University of Faisalabad

Comparative Effects of Coordinative Locomotor Training Using Sprinter Versus Skater Coordination Synergies on Balance and Coordination in Patients With Chronic Stroke: A Randomized Clinical Trial

This study compares two types of coordinative locomotor training - the sprinter coordination synergy and the skater coordination synergy - to improve balance and coordination in people with chronic stroke (more than six months after stroke). Twenty two participants will be randomly assigned to receive either sprinter-based or skater-based training for 30 minutes per session, three times per week, for four weeks. Balance will be measured using the Berg Balance Scale and Functional Reach Test. Coordination and functional mobility will be measured using the Timed Up and Go test. This study aims to determine which coordination synergy produces greater improvements, which may help physiotherapists choose more effective treatments for stroke survivors in Pakistan.

Panoramica dello studio

Descrizione dettagliata

Background: Chronic stroke survivors often experience persistent deficits in balance and coordination due to damage to motor control pathways in the brain. These deficits limit independence, increase fall risk, and reduce quality of life. Coordinative Locomotor Training (CLT) is a rehabilitation approach that integrates Proprioceptive Neuromuscular Facilitation (PNF) patterns with whole-body movement sequences. The sprinter coordination synergy mimics a runner's movement: on one side, the upper extremity moves into flexion, adduction, and external rotation while the ipsilateral lower extremity moves into extension, adduction, and internal rotation. The skater coordination synergy mimics a speed skater: on one side, the upper extremity moves into flexion, abduction, and external rotation while the lower extremity moves into extension, adduction, and external rotation. Both patterns activate the whole body with one leg functioning in a closed chain position.

Objectives: To compare the effects of sprinter coordination synergy versus skater coordination synergy on: (1) static and dynamic balance measured by Berg Balance Scale (BBS) and Functional Reach Test (FRT); (2) coordination and functional mobility measured by Timed Up and Go (TUG) test. Secondary objectives include determining which technique shows significantly greater improvement and providing evidence-based recommendations for physiotherapy practice in Pakistan.

Study Design: Randomized, parallel-group, double-blind clinical trial.

Setting: Outpatient rehabilitation department, Aziz Fatima Hospital and In Motion Clinic, Faisalabad, Punjab, Pakistan.

Sample Size: Twenty-two participants (11 per group). Sample size calculated based on effect sizes from previous similar studies (Kim, Lee and Jung, 2015), with 20% allowance for attrition (n=4).

Eligibility Criteria: Adults aged 30-60 years with a physician-diagnosed ischemic or hemorrhagic stroke occurring at least six months prior. Participants must be able to stand or walk independently for at least 10 meters (with or without assistive device) and follow verbal instructions. Exclusion criteria include visual or hearing deficits, vestibular dysfunction, orthopedic disorders affecting movement, other neurological disorders, or any contraindication to exercise.

Intervention Protocol: Both groups receive 30-minute sessions, three times per week, for four weeks (total 12 sessions). Group A (n=11) performs CLT using the sprinter coordination synergy . Group B (n=11) performs CLT using the skater coordination synergy. Both interventions are delivered by a trained physiotherapist using standardized PNF techniques. Participants perform the patterns in four postures: supine, sitting, standing, and walking with support as tolerated. Each pattern is performed for 30-60 seconds per posture, repeated 5-10 times with rest periods as needed.

Outcome Measures: Assessments occur at baseline (pre-intervention, week 0) and after the final intervention session (week 4). Primary outcomes: Berg Balance Scale (14 items, scored 0-56, higher scores indicate better balance) and Functional Reach Test (distance in centimeters, greater distance indicates better dynamic balance), Timed Up and Go test (seconds to stand from chair, walk 3 meters, turn, return, and sit; shorter times indicate better functional mobility and coordination).

Statistical Analysis: Intention-to-treat analysis will be used. Normality of data will be assessed by Shapiro-Wilk test. Within-group comparisons will use paired t-test for normally distributed data or Wilcoxon signed-rank test for non-normal data. Between-group comparisons will use independent t-test or Mann-Whitney U test. Significance level set at p ≤ 0.05. Results will be presented in graphical and tabular form using SPSS version (latest available).

Expected Outcomes: Both sprinter and skater coordination synergy are expected to improve balance and coordination. This study will identify whether one coordination synergy produces superior results, providing evidence for targeted rehabilitation programs for chronic stroke patients in Pakistan.

Tipo di studio

Interventistico

Iscrizione (Stimato)

22

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Punjan
      • Faisalābad, Punjan, Pakistan, 38000
        • Department of Rehabilitation Sciences, The University of Faisalabad

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

  • Adulto

Accetta volontari sani

Descrizione

Inclusion Criteria:

  • Physician-diagnosed ischemic or hemorrhagic stroke
  • Age between 30 and 60 years, inclusive
  • Both male and female participants
  • Time since stroke onset: 6 months or more (chronic stage)
  • Able to stand or walk independently for at least 10 meters (with or without assistive device)
  • Able to follow verbal instructions (Mini-Mental State Examination score ≥ 24 or equivalent clinical judgment)
  • Able to provide informed consent

Exclusion Criteria:

  • Visual impairment that interferes with movement coordination
  • Hearing deficit that prevents following instructions
  • Vestibular dysfunction affecting balance
  • Orthopedic disorders (fracture, joint deformity, severe arthritis, joint replacement) limiting movement
  • Other neurological disorders besides stroke (Parkinson's disease, multiple sclerosis, peripheral neuropathy)
  • Contraindication to exercise as advised by physician
  • Participation in another interventional rehabilitation study concurrently

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

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

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Sprinter Coordination Synergy Group
Participants receive Coordinative Locomotor Training using the sprinter coordination synergy for 30 minutes per session, three times per week, for four weeks (total 12 sessions). The sprinter pattern mimics a runner's movement: on one side of the body, the upper extremity moves into flexion, adduction, and external rotation while the ipsilateral lower extremity moves into extension, adduction, and internal rotation. The opposite side performs the reciprocal pattern. Training is performed in four postures: supine, sitting, standing, and walking with support as tolerated. Each pattern is performed for 30-60 seconds per posture, repeated 5-10 times with rest periods as needed.
What: Coordinative Locomotor Training using the sprinter coordination synergy. How: A trained physiotherapist manually guides the participant through diagonal, rotational movement patterns of upper and lower extremities simultaneously. The sprinter pattern involves: on one side, upper extremity flexion/adduction/external rotation with ipsilateral lower extremity extension/adduction/internal rotation; the contralateral side performs the reciprocal pattern. When: 30 minutes per session, 3 sessions per week, for 4 consecutive weeks (total 12 sessions). How much: Each pattern performed for 30-60 seconds per posture (supine, sitting, standing, walking), repeated 5-10 times with rest periods as needed. By whom: Physiotherapist trained in PNF and CLT techniques.
Sperimentale: Skater Coordination Synergy Group
Participants receive Coordinative Locomotor Training using the skater coordination synergy for 30 minutes per session, three times per week, for four weeks (total 12 sessions). The skater pattern mimics a speed skater's movement: on one side of the body, the upper extremity moves into flexion, abduction, and external rotation while the ipsilateral lower extremity moves into extension, adduction, and external rotation. The opposite side performs the reciprocal pattern. Training is performed in four postures: supine, sitting, standing, and walking with support as tolerated. Each pattern is performed for 30-60 seconds per posture, repeated 5-10 times with rest periods as needed.
What: Coordinative Locomotor Training using the skater coordination synergy . How: A trained physiotherapist manually guides the participant through diagonal, rotational movement patterns mimicking a speed skater. The skater pattern involves: on one side, upper extremity flexion/abduction/external rotation with ipsilateral lower extremity extension/adduction/external rotation; the contralateral side performs the reciprocal pattern. When: 30 minutes per session, 3 sessions per week, for 4 consecutive weeks (total 12 sessions). How much: Each pattern performed for 30-60 seconds per posture (supine, sitting, standing, walking), repeated 5-10 times with rest periods as needed. By whom: Physiotherapist trained in PNF and CLT techniques.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in Balance as Measured by the Berg Balance Scale
Lasso di tempo: Baseline (week 0, before first intervention session) and post-intervention (week 4, within 48 hours after the final intervention session)
The Berg Balance Scale (BBS) is a 14-item objective measure of static and dynamic balance. Each item is scored from 0 (unable to perform) to 4 (independent performance). Total scores range from 0 to 56. Higher scores indicate better balance. Interpretation: 41-56 = low fall risk, 21-40 = medium fall risk, 0-20 = high fall risk. The scale is widely used in stroke rehabilitation research and has excellent reliability and validity.
Baseline (week 0, before first intervention session) and post-intervention (week 4, within 48 hours after the final intervention session)
Change in Dynamic Balance as Measured by the Functional Reach Test
Lasso di tempo: Baseline (week 0, before first intervention session) and post-intervention (week 4, within 48 hours after the final intervention session)
The Functional Reach Test (FRT) measures the maximum distance a person can reach forward from a standing position while maintaining a fixed base of support. Distance is measured in centimeters. Greater reach distance indicates better dynamic balance. Int
Baseline (week 0, before first intervention session) and post-intervention (week 4, within 48 hours after the final intervention session)
Change in Functional Mobility and Coordination as Measured by the Timed Up and Go Test
Lasso di tempo: Baseline (week 0, before first intervention session) and post-intervention (week 4, within 48 hours after the final intervention session)
The Timed Up and Go (TUG) test measures the time in seconds required to stand up from a standard armchair (seat height approximately 46 cm), walk 3 meters at a comfortable and safe pace, turn around, walk back to the chair, and sit down again. Shorter ti
Baseline (week 0, before first intervention session) and post-intervention (week 4, within 48 hours after the final intervention session)

Collaboratori e investigatori

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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)

1 febbraio 2026

Completamento primario (Stimato)

15 giugno 2026

Completamento dello studio (Stimato)

1 luglio 2026

Date di iscrizione allo studio

Primo inviato

10 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

15 giugno 2026

Primo Inserito (Effettivo)

22 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

22 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

15 giugno 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • 2021-D-PT-086
  • TUF/EIRB/252/26 (Altro identificatore: The University of Faisalabad)

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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