Diese Seite wurde automatisch übersetzt und die Genauigkeit der Übersetzung wird nicht garantiert. Bitte wende dich an die englische Version für einen Quelltext.

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

9. Juli 2026 aktualisiert von: 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.

Studienübersicht

Detaillierte Beschreibung

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.

Studientyp

Interventionell

Einschreibung (Tatsächlich)

5

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

    • Antioquia
      • Guarne, Antioquia, Kolumbien, 054080
        • Tecnológico de Antioquia

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Kind
  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Ja

Beschreibung

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.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Sonstiges
  • Zuteilung: N / A
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
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.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Change from baseline in main-event finswimming performance time
Zeitfenster: 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

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Change from baseline in mean swimming velocity
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

1. April 2026

Primärer Abschluss (Tatsächlich)

1. April 2026

Studienabschluss (Tatsächlich)

2. Mai 2026

Studienanmeldedaten

Zuerst eingereicht

2. Juli 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

2. Juli 2026

Zuerst gepostet (Tatsächlich)

9. Juli 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

13. Juli 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

9. Juli 2026

Zuletzt verifiziert

1. Juli 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • LVHI-Finswimmers-TdeA

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Beschreibung des IPD-Plans

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.

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

Abonnieren