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Isometric Core Training and Swimming Performance in Adolescent Amputee Swimmers

28 de mayo de 2026 actualizado por: Görkem Açar, Istanbul Gelisim University

Effects of a 12-Week Isometric Core Training Program on Trunk Endurance and 50-m Freestyle Performance in Adolescent Amputee Swimmers: A Randomized Controlled Trial

Adolescent amputee swimmers often experience challenges related to trunk stabilization, postural control, and efficient force transfer during swimming because of asymmetric biomechanics associated with limb loss. Core muscle training has been proposed as a potential dryland conditioning strategy to support swimming performance and trunk endurance in Para-swimmers; however, evidence from randomized controlled trials in adolescent amputee swimmers remains limited.

The purpose of this study is to investigate the effects of a 12-week supervised isometric core training program on trunk muscular endurance and 50-meter freestyle swimming performance in adolescent amputee swimmers. Participants will be randomly assigned to either an experimental group receiving additional isometric core training together with standard swimming training or a control group performing standard swimming training only.

Primary outcome measures will include 50-meter freestyle performance time. Secondary outcome measures will include trunk muscular endurance assessments such as the 20-second sit-up test, 20-second reverse sit-up test, supine bent-knee leg hold, and prone trunk-extension hold. Assessments will be performed before and after the 12-week intervention period.

The findings of this study may contribute to the development of evidence-based dryland conditioning programs for adolescent Para-swimmers with limb amputations.

Descripción general del estudio

Tipo de estudio

Intervencionista

Inscripción (Actual)

30

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

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

  • Niño
  • Adulto

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  • Upper- or lower-limb amputation
  • Participation in at least two consecutive Turkish National Para-swimming -Championships
  • Active training with regular competitive participation
  • Age between 14 and 20 years
  • Ability to participate in regular swimming and exercise training
  • Written informed consent obtained from participants and/or parents/guardians

Exclusion Criteria:

  • Discontinuation of regular training or competitive participation
  • Acute musculoskeletal injury or cardiovascular condition preventing maximal exercise participation
  • Refusal or inability to participate in the study protocol
  • Failure to complete the intervention or assessment procedures

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: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Experimental Group
Participants in the experimental group completed a 12-week supervised isometric core training program in addition to their regular swimming training. The intervention was performed three times per week and included individualized trunk stabilization and endurance exercises adapted to the athlete's level of amputation.
Participants assigned to the experimental group completed a supervised 12-week isometric core training program in addition to their regular swimming training. The intervention was performed three times per week and included individualized exercises targeting trunk stabilization, abdominal endurance, and lumbopelvic control. Exercises were adapted according to the athlete's level of upper- or lower-limb amputation and included front plank, side plank, trunk-extension holds, bridge exercises, Pallof press holds, and bird-dog/dead-bug variations. Training duration and resistance were progressively increased throughout the intervention period.
Comparador activo: Control Group
Participants in the control group continued their regular swimming training program for 12 weeks without additional dryland core training.
Participants assigned to the control group continued their regular swimming training program for 12 weeks without any additional dryland core training intervention. The swimming program consisted of routine in-water training sessions conducted at the Ankara Olympic Preparation Centre according to the standard preparation program for competitive Para-swimmers.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
50-m Freestyle Swimming Performance
Periodo de tiempo: Baseline and after 12 weeks of intervention
Official 50-m freestyle race time measured using FINA-approved electronic timing equipment during national Para-swimming competitions.
Baseline and after 12 weeks of intervention

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
20-second Sit-up Performance
Periodo de tiempo: Baseline and after 12 weeks of intervention
Number of correctly completed sit-up repetitions performed within 20 seconds to assess trunk flexor endurance.
Baseline and after 12 weeks of intervention
20-second Reverse Sit-up Performance
Periodo de tiempo: Baseline and after 12 weeks of intervention
Number of correctly completed reverse sit-up repetitions performed within 20 seconds to assess trunk extensor endurance.
Baseline and after 12 weeks of intervention
Supine Bent-knee Leg Hold Duration
Periodo de tiempo: Baseline and after 12 weeks of intervention
Duration in seconds that participants maintained the supine bent-knee leg hold position to assess lumbopelvic endurance.
Baseline and after 12 weeks of intervention
Prone Trunk-extension Hold Duration
Periodo de tiempo: Baseline and after 12 weeks of intervention
Duration in seconds that participants maintained the prone trunk-extension hold position to assess trunk extensor endurance.
Baseline and after 12 weeks of intervention

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 marzo de 2024

Finalización primaria (Actual)

1 de junio de 2024

Finalización del estudio (Actual)

1 de junio de 2024

Fechas de registro del estudio

Enviado por primera vez

7 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

28 de mayo de 2026

Publicado por primera vez (Actual)

2 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

2 de junio de 2026

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

28 de mayo de 2026

Última verificación

1 de mayo de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • 2024-03-73

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

INDECISO

Descripción del plan IPD

Individual participant data sharing has not yet been determined. Data may be shared upon reasonable request after publication of the study results and following approval by the corresponding author and institutional ethics requirements. Participant confidentiality and privacy protections will be maintained.

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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