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

9. července 2026 aktualizováno: 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.

Přehled studie

Detailní popis

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.

Typ studie

Intervenční

Zápis (Aktuální)

5

Fáze

  • Nelze použít

Kontakty a umístění

Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.

Studijní místa

    • Antioquia
      • Guarne, Antioquia, Kolumbie, 054080
        • Tecnológico de Antioquia

Kritéria účasti

Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.

Kritéria způsobilosti

Věk způsobilý ke studiu

  • Dítě
  • Dospělý
  • Starší dospělý

Přijímá zdravé dobrovolníky

Ano

Popis

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.

Studijní plán

Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.

Jak je studie koncipována?

Detaily designu

  • Primární účel: Jiný
  • Přidělení: N/A
  • Intervenční model: Přiřazení jedné skupiny
  • Maskování: Žádné (otevřený štítek)

Zbraně a zásahy

Skupina účastníků / Arm
Intervence / Léčba
Experimentální: 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.

Co je měření studie?

Primární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Change from baseline in main-event finswimming performance time
Časové okno: 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

Sekundární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Change from baseline in mean swimming velocity
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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

Spolupracovníci a vyšetřovatelé

Zde najdete lidi a organizace zapojené do této studie.

Termíny studijních záznamů

Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.

Hlavní termíny studia

Začátek studia (Aktuální)

1. dubna 2026

Primární dokončení (Aktuální)

1. dubna 2026

Dokončení studie (Aktuální)

2. května 2026

Termíny zápisu do studia

První předloženo

2. července 2026

První předloženo, které splnilo kritéria kontroly kvality

2. července 2026

První zveřejněno (Aktuální)

9. července 2026

Aktualizace studijních záznamů

Poslední zveřejněná aktualizace (Aktuální)

13. července 2026

Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality

9. července 2026

Naposledy ověřeno

1. července 2026

Více informací

Termíny související s touto studií

Další identifikační čísla studie

  • LVHI-Finswimmers-TdeA

Plán pro data jednotlivých účastníků (IPD)

Plánujete sdílet data jednotlivých účastníků (IPD)?

NE

Popis plánu 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.

Informace o lécích a zařízeních, studijní dokumenty

Studuje lékový produkt regulovaný americkým FDA

Ne

Studuje produkt zařízení regulovaný americkým úřadem FDA

Ne

Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .

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