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Isometric Core Training and Swimming Performance in Adolescent Amputee Swimmers

28 mei 2026 bijgewerkt door: 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.

Studie Overzicht

Studietype

Ingrijpend

Inschrijving (Werkelijk)

30

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Kind
  • Volwassen

Accepteert gezonde vrijwilligers

Nee

Beschrijving

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

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Enkel

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: 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.
Actieve vergelijker: 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.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
50-m Freestyle Swimming Performance
Tijdsspanne: 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

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
20-second Sit-up Performance
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

1 maart 2024

Primaire voltooiing (Werkelijk)

1 juni 2024

Studie voltooiing (Werkelijk)

1 juni 2024

Studieregistratiedata

Eerst ingediend

7 mei 2026

Eerst ingediend dat voldeed aan de QC-criteria

28 mei 2026

Eerst geplaatst (Werkelijk)

2 juni 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

2 juni 2026

Laatste update ingediend die voldeed aan QC-criteria

28 mei 2026

Laatst geverifieerd

1 mei 2026

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • 2024-03-73

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

ONBESLIST

Beschrijving IPD-plan

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.

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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