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

9. juli 2026 oppdatert av: 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.

Studieoversikt

Detaljert beskrivelse

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.

Studietype

Intervensjonell

Registrering (Faktiske)

5

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Antioquia
      • Guarne, Antioquia, Colombia, 054080
        • Tecnológico de Antioquia

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn
  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Ja

Beskrivelse

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.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Annen
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change from baseline in main-event finswimming performance time
Tidsramme: 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

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change from baseline in mean swimming velocity
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

1. april 2026

Primær fullføring (Faktiske)

1. april 2026

Studiet fullført (Faktiske)

2. mai 2026

Datoer for studieregistrering

Først innsendt

2. juli 2026

Først innsendt som oppfylte QC-kriteriene

2. juli 2026

Først lagt ut (Faktiske)

9. juli 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

13. juli 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

9. juli 2026

Sist bekreftet

1. juli 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • LVHI-Finswimmers-TdeA

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

IPD-planbeskrivelse

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.

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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