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

3 november 2026 uppdaterad av: 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.

Studieöversikt

Studietyp

Interventionell

Inskrivning (Beräknad)

12

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

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

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år till 22 år (Vuxen)

Tar emot friska volontärer

Ja

Kön som är behöriga för studier

Manlig

Beskrivning

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

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Övrig
  • Tilldelning: Randomiserad
  • Interventionsmodell: Crossover tilldelning
  • Maskning: Enda

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Sham Comparator: 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.

Experimentell: 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.

Experimentell: 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.

Inget ingripande: Control

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

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Peak Power ( 60°/s)
Tidsram: 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)
Tidsram: 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)
Tidsram: 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)
Tidsram: 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)
Tidsram: 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)
Tidsram: 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

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
H/Q ratio
Tidsram: 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
Tidsram: 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
Tidsram: 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

Samarbetspartners och utredare

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Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Beräknad)

1 december 2026

Primärt slutförande (Beräknad)

31 december 2026

Avslutad studie (Beräknad)

31 december 2026

Studieregistreringsdatum

Först inskickad

27 oktober 2026

Först inskickad som uppfyllde QC-kriterierna

3 november 2026

Första postat (Faktisk)

9 november 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

9 november 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

3 november 2026

Senast verifierad

1 november 2026

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • 2026/9504

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

NEJ

IPD-planbeskrivning

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

Läkemedels- och apparatinformation, studiedokument

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Nej

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Nej

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