Deze pagina is automatisch vertaald en de nauwkeurigheid van de vertaling kan niet worden gegarandeerd. Raadpleeg de Engelse versie voor een brontekst.

Inspiratory Muscle Training Plus Cold Water Immersion After Muscle-Damaging Exercise

3 november 2026 bijgewerkt door: Mete Berk Demiryol, University of Gaziantep

The Combined Effect of Cold Water Immersion and Inspiratory Muscle Training on the Recovery From Exercise-Induced Muscle Damage and Physical Performance: A Randomized, Placebo-Controlled Crossover Study

The purpose of this study is to examine, using a placebo-controlled design, the additional effect of inspiratory muscle training (IMT) added to cold water immersion (CWI) on recovery and muscle performance following exercise-induced muscle damage (EIMD), and to determine whether this effect varies depending on the timing of the intervention. The study will include 12 healthy male athletes aged 18-22 who have been licensed for at least 4 years and are actively involved in sports. Each participant will undergo four different interventions in a randomized order determined by the Williams balanced sequence following muscle damage induced by eccentric exercise on an isokinetic dynamometer: CWI + placebo IMT immediately after exercise, IMT + CWI immediately after exercise, IMT + CWI 24 hours after exercise, and a control condition with no recovery intervention. The sessions will be conducted in weekly cycles with 7-day intervals, alternating between the dominant and non-dominant legs; thus, there will be a 14-day interval between two loading sessions for the same leg. All measurements will be taken during the week. Muscle strength will be assessed using an isokinetic dynamometer; markers of muscle damage (CK, myoglobin, LDH) will be measured via blood samples; and muscle pain will be evaluated using the Visual Analog Scale (VAS) before each exercise session and 48 hours after exercise.

Studie Overzicht

Studietype

Ingrijpend

Inschrijving (Geschat)

12

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

    • Şehitkamil
      • Gaziantep, Şehitkamil, Turkije (Türkiye)
        • Gaziantep University, Faculty of Sports Sciences, Sports Performance and Testing Laboratory

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

18 jaar tot 22 jaar (Volwassen)

Accepteert gezonde vrijwilligers

Ja

Geslachten die in aanmerking komen voor studie

Mannelijk

Beschrijving

Inclusion Criteria:

  • Be a male between the ages of 18 and 22
  • Hold a sports license valid for at least 4 years
  • Be actively involved in sports
  • Not smoke or use similar substances

Exclusion Criteria:

  • Having sustained a sports injury within the past 2 years
  • Having engaged in exercise that could cause muscle damage within the past 15 days
  • Cold intolerance, cold urticaria, or Raynaud's phenomenon
  • Known cardiovascular, respiratory, or musculoskeletal disease
  • Use of anti-inflammatory medication or dietary supplements that could affect recovery during the study period

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: Ander
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Crossover-opdracht
  • Masker: Enkel

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Sham-vergelijker: CWI + placebo IMT

Device: Placebo IMT - 2 × 30 breaths at 15% of MIP using POWERbreathe (1 min between sets), immediately following the short test after EIMD. Other: Immersion in cold water - immediately following the placebo IMT, in 10-12 °C water, up to waist level or with legs fully submerged, for 10-15 minutes.

Immersion up to the waist in water at 13-15 °C for 13-15 minutes in a portable ice bath; water temperature is monitored with a thermometer and maintained by adding ice.

Same device, position and volume as inspiratory muscle training (two sets of 30 breaths, 1 minute rest), but at 15% of maximal inspiratory pressure, a load considered below the training threshold. Followed immediately by cold water immersion.

Experimenteel: IMT + CWI (immediately)

Other: Inspiratory muscle training + cold water immersion. Immediately following the short test after EIMD, 2 × 30 breaths at 40% of MIP using POWERbreathe (1 min rest between sets), followed by CWI.

Immersion up to the waist in water at 13-15 °C for 13-15 minutes in a portable ice bath; water temperature is monitored with a thermometer and maintained by adding ice.

Two sets of 30 breaths at 40% of maximal inspiratory pressure with 1 minute rest between sets, using a POWERbreathe device; oxygen saturation is monitored by pulse oximetry. Followed immediately by cold water immersion.

Experimenteel: IMT + CWI (at 24 hours)

Other: Inspiratory muscle training + cold water immersion. The same IMT and CWI protocol is administered 24 hours after EIMD; the 48-hour measurement is taken relative to EIMD (24 hours after the intervention).

Immersion up to the waist in water at 13-15 °C for 13-15 minutes in a portable ice bath; water temperature is monitored with a thermometer and maintained by adding ice.

Two sets of 30 breaths at 40% of maximal inspiratory pressure with 1 minute rest between sets, using a POWERbreathe device; oxygen saturation is monitored by pulse oximetry. Followed immediately by cold water immersion.

Geen tussenkomst: Control

No recovery procedure is performed after the EIMD protocol; only measurements are taken.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Peak Power ( 60°/s)
Tijdsspanne: The 48-hour period before and after EIMD in each phase

Highest torque (Nm) measured during a 5-rep maximum test on an isokinetic dynamometer

The 48-hour period before and after EIMD in each phase
Peak Power ( 180°/s)
Tijdsspanne: The 48-hour period before and after EIMD in each phase

Highest torque (Nm) measured during a 10-rep maximum test on an isokinetic dynamometer

The 48-hour period before and after EIMD in each phase
Average Power ( 180°/s- 60°/s)
Tijdsspanne: The 48-hour period before and after EIMD in each phase

Average of peak torque values during test repetitions (Nm)

The 48-hour period before and after EIMD in each phase
Serum creatine kinase (CK)
Tijdsspanne: The 48-hour period before and after EIMD in each phase

CK level in venous blood (U/L)

The 48-hour period before and after EIMD in each phase
Myoglobin (Mb)
Tijdsspanne: The 48-hour period before and after EIMD in each phase

Myoglobin level in venous blood (ng/mL)

The 48-hour period before and after EIMD in each phase
Lactate dehydrogenase (LDH)
Tijdsspanne: The 48-hour period before and after EIMD in each phase

LDH level in venous blood (U/L)

The 48-hour period before and after EIMD in each phase

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
H/Q ratio
Tijdsspanne: The 48-hour period before and after EIMD in each phase

Hamstring-to-quadriceps peak torque ratio (60°/s and 180°/s)

The 48-hour period before and after EIMD in each phase
VAS
Tijdsspanne: During each period: before EIMD, immediately after EIMD, and 48 hours after EIMD

0-10 cm Visual Analog Scale (0 = no pain, 10 = very severe pain)

During each period: before EIMD, immediately after EIMD, and 48 hours after EIMD
Fatique Index
Tijdsspanne: The 48-hour period before and after EIMD in each phase

Fatigue index (%) calculated from a test consisting of 10 cycles at 180°/s

The 48-hour period before and after EIMD in each phase

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 (Geschat)

1 december 2026

Primaire voltooiing (Geschat)

31 december 2026

Studie voltooiing (Geschat)

31 december 2026

Studieregistratiedata

Eerst ingediend

27 oktober 2026

Eerst ingediend dat voldeed aan de QC-criteria

3 november 2026

Eerst geplaatst (Werkelijk)

9 november 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

9 november 2026

Laatste update ingediend die voldeed aan QC-criteria

3 november 2026

Laatst geverifieerd

1 november 2026

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • 2026/9504

Plan Individuele Deelnemersgegevens (IPD)

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

NEE

Beschrijving IPD-plan

"Individual participant data will not be shared for privacy reasons; aggregate results will be published."

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

Abonneren