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

15 de junio de 2026 actualizado por: 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.

Descripción general del estudio

Descripción detallada

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 de estudio

Intervencionista

Inscripción (Estimado)

22

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

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

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto

Acepta Voluntarios Saludables

Descripción

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

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Doble

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: 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.
Experimental: 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.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in Balance as Measured by the Berg Balance Scale
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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)

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

1 de febrero de 2026

Finalización primaria (Estimado)

15 de junio de 2026

Finalización del estudio (Estimado)

1 de julio de 2026

Fechas de registro del estudio

Enviado por primera vez

10 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

15 de junio de 2026

Publicado por primera vez (Actual)

22 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

22 de junio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

15 de junio de 2026

Última verificación

1 de junio de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

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

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

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