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Low-Volume High-Intensity Race-Pace Training in Finswimmers (LVHI-FS-TdeA)

9 de julho de 2026 atualizado por: Édison Andrés Pérez Bedoya, Federal University of Vicosa

Individual Responses to a Low-Volume, High-Intensity Race-Pace Training Block in Finswimmers From the Antioquia Underwater Activities League: A Prospective Single-Group Case Series

This single-group case series describe individual responses to a 9-week low-volume, high-intensity race-pace training block in 5 finswimmers from the Antioquia Underwater Activities League (LASA), Colombia. The intervention will be oriented towards race-specific swimming paces and will include repeated swimming efforts prescribed according to each athlete's main competitive event. External training load, heart rate, rating of perceived exertion, pace stability, and sport performance were monitored throughout the block. The primary outcome was the change in performance time in each athlete's main competitive event from baseline to post-intervention. The study used an intra-individual descriptive approach and did not include randomisation, a control group, or causal inference.

Visão geral do estudo

Descrição detalhada

Finswimming is a high-speed aquatic sport in which performance in short and middle-distance events depends on the ability to produce and sustain race-specific velocity. Traditional aquatic training models often emphasise high training volume; however, for events lasting from seconds to a few minutes, race-pace work, neuromuscular quality, and individualised load monitoring may be particularly relevant.

This study follows 5 finswimmers from the Antioquia Underwater Activities League (LASA) during a 9-week low-volume, high-intensity training block. All participants received the same general training approach, but training distances, repetitions, target times, and race-pace references were individualised according to each athlete's main competitive event.

Before the intervention, athletes completed a basic characterisation and a baseline performance assessment using an official competition result. Training target times were estimated from the baseline performance. During the 9-week block, the investigators recorded external load variables, including distance, repetitions, weekly volume, target time, and actual time for each relevant repetition. Internal load were monitored using heart rate and rating of perceived exertion. Pace stability were estimated from repeated times in event-specific distances using descriptive indicators such as mean time, standard deviation, and coefficient of variation.

After the intervention, performance were reassessed in the athlete's main event through an official competition or a comparable standardised control test. Data analysis were focus on individual responses, weekly trends, and descriptive changes from baseline to post-intervention. The study were not include a control group or randomisation; therefore, findings were interpreted as exploratory and non-causal.

Tipo de estudo

Intervencional

Inscrição (Real)

5

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • Antioquia
      • Guarne, Antioquia, Colômbia, 054080
        • Tecnológico de Antioquia

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Filho
  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Sim

Descrição

Inclusion Criteria:

  • Finswimmers affiliated with the Antioquia Underwater Activities League (LASA).
  • Regular participation in finswimming training.
  • A defined main competitive event.
  • Availability to complete the 9-week follow-up period.
  • Ability to complete high-intensity swimming training according to the regular sport programme.
  • Written informed consent from adult participants.
  • For participants under 18 years of age, written informed consent from a parent or legal guardian and written assent from the participant.

Exclusion Criteria:

  • Active musculoskeletal injury.
  • Relevant pain or acute illness at baseline.
  • Medical restriction for high-intensity swimming exercise.
  • Inability to complete the planned follow-up.
  • Withdrawal of consent or assent.
  • Insufficient attendance or incomplete records for the main study variables.
  • Any condition judged by the research team or coaching staff to compromise participant safety during high-intensity swimming.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Outro
  • Alocação: N / D
  • Modelo Intervencional: Atribuição de grupo único
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Low-volume high-intensity race-pace finswimming training
Participants will complete a 9-week finswimming training block focused on low-volume, high-intensity, race-pace swimming. Training will be individualised according to each athlete's main competitive event and monitored using external load, heart rate, rating of perceived exertion, and repetition times.
The intervention will consist of a 9-week finswimming training block oriented towards race-specific pace. Participants will perform repeated swimming efforts prescribed according to individual target times derived from baseline performance. Training sessions will include event-specific distances, repetitions, recovery periods, and target intensities. External load will be monitored through distance, repetitions, weekly volume, target time, and actual time. Internal load will be monitored using heart rate and rating of perceived exertion. Training volume will be adjusted according to the athlete's event profile and reduced towards the final phase when tapering is required.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Change from baseline in main-event finswimming performance time
Prazo: Baseline and week 9
Performance time, in seconds, will be recorded for each participant's main competitive event. The baseline value will be obtained from an official competition result or a standardised control test before the training block. The post-intervention value will be obtained from an official competition result or a comparable standardised control test after the 9-week block. A lower time will indicate better performance.
Baseline and week 9

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Change from baseline in mean swimming velocity
Prazo: Baseline and week 9
Mean swimming velocity will be calculated from the performance distance and time in each participant's main event. Velocity will be expressed in metres per second. A higher value will indicate better performance.
Baseline and week 9
Weekly external training volume
Prazo: Weekly from baseline to week 9
External training volume will be quantified as the total metres completed per week during recorded race-pace or event-specific swimming repetitions.
Weekly from baseline to week 9
Weekly mean heart rate during recorded swimming repetitions
Prazo: Weekly from baseline to week 9
Heart rate will be recorded during training sessions using a heart rate monitor, sport watch, or equivalent device. Weekly mean heart rate will be reported in beats per minute.
Weekly from baseline to week 9
Weekly rating of perceived exertion
Prazo: Weekly from baseline to week 9
Rating of perceived exertion will be recorded using a numerical perceived exertion scale after relevant sets or at the end of the session, according to the predefined monitoring protocol. Weekly mean values will be described for each participant.
Weekly from baseline to week 9
Pace stability during event-specific swimming repetitions
Prazo: Repeated training sessions from baseline to week 9
Pace stability will be estimated from repeated swimming times in event-specific distances. The coefficient of variation will be calculated for each participant and distance when repeated measurements are available. Lower values will indicate greater pace stability.
Repeated training sessions from baseline to week 9

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

1 de abril de 2026

Conclusão Primária (Real)

1 de abril de 2026

Conclusão do estudo (Real)

2 de maio de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

2 de julho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

2 de julho de 2026

Primeira postagem (Real)

9 de julho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

13 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

9 de julho de 2026

Última verificação

1 de julho de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • LVHI-Finswimmers-TdeA

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Descrição do plano IPD

Individual participant data will not be publicly shared because the study will include a small number of athletes from a specific sport league, which may increase the risk of re-identification even after anonymisation. De-identified aggregate data, data dictionaries, and analysis procedures may be made available upon reasonable request, subject to ethics approval and institutional data protection requirements.

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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