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

Acute Changes in Gastrocnemius Muscle Stiffness

30 juli 2026 bijgewerkt door: Monira Aldhahi, Princess Nourah Bint Abdulrahman University

Acute Changes in Gastrocnemius Muscle Stiffness Following Different Work-Rest Calf-Raise Protocols and Percussive Therapy: A Randomized Crossover Experimental Study

This study evaluated how different exercise and rest schedules during calf-raise exercise affected the stiffness of the calf muscle in trained volleyball athletes. It also examined how muscle stiffness changed during a five-minute recovery period in which percussive therapy was applied.

Thirty volleyball athletes, including 15 women and 15 men, completed three exercise sessions in a randomized order. During each session, participants performed repeated calf raises for a total period of five minutes using one of three work-to-rest schedules: 30 seconds of exercise followed by 30 seconds of rest, 15 seconds of exercise followed by 45 seconds of rest, or 45 seconds of exercise followed by 15 seconds of rest.

The stiffness of the medial gastrocnemius, one of the main calf muscles, was measured using shear-wave elastography. Measurements were taken before exercise, immediately after exercise, and after the five-minute percussive therapy recovery period.

Studie Overzicht

Gedetailleerde beschrijving

This randomized, three-period crossover study examined the acute effects of different work-to-rest configurations during a standardized bilateral calf-raise exercise on medial gastrocnemius stiffness in trained volleyball athletes.

Thirty participants, comprising 15 women and 15 men, completed three experimental sessions in a computer-generated randomized order. Sessions were separated by at least 48 hours and were conducted at approximately the same time of day for each participant to reduce the effects of fatigue, carryover, and daily variation. Before data collection, participants completed a familiarization session.

Each experimental session lasted five minutes and included one of the following work-to-rest configurations:

30 seconds of calf raises followed by 30 seconds of rest; 15 seconds of calf raises followed by 45 seconds of rest; or 45 seconds of calf raises followed by 15 seconds of rest.

The exercise cadence was standardized at one repetition per second using a metronome. Participants performed the calf raises barefoot, with their feet approximately shoulder-width apart and their hands placed on their hips. The total session duration was the same for all conditions, while the amount and distribution of exercise and rest differed between protocols.

Medial gastrocnemius stiffness was assessed bilaterally using shear-wave elastography. Measurements were obtained before exercise, immediately after completion of the calf-raise protocol, and after a standardized five-minute recovery period involving percussive therapy. Three elastography acquisitions were recorded for each leg at each assessment and were averaged for analysis.

Percussive therapy was applied to both medial gastrocnemius muscles using a Theragun PRO device with a spherical attachment at approximately 1,750 percussions per minute. Each leg received two 60-second applications separated by 30 seconds of rest. The same experienced researcher administered the intervention and performed the measurements during all sessions.

The primary analysis evaluated changes in shear-wave velocity across the three measurement times and compared those changes among the three exercise protocols. Limb side and participant sex were also examined as exploratory factors.

The primary hypothesis was that the protocol containing 45 seconds of exercise and 15 seconds of rest would produce the greatest immediate increase in gastrocnemius stiffness because it had the highest work density. A secondary objective was to examine whether stiffness decreased toward baseline during the subsequent percussive therapy recovery period.

No sham percussive therapy or passive recovery condition was included. Therefore, changes between the immediate post-exercise and final assessments were interpreted as recovery occurring during the percussive therapy period and not as definitive evidence of an isolated treatment effect

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

  • Volwassen

Accepteert gezonde vrijwilligers

Ja

Beschrijving

Inclusion Criteria:

  • Male or female volleyball athlete aged 18 to 30 years.
  • Competing at university or club level.
  • At least 3 years of structured volleyball training experience.
  • Participating in volleyball training at least 3 times per week.
  • Body mass index between 18.5 and 27.0 kg/m².
  • No lower-limb musculoskeletal injury during the previous 6 months.
  • No known neuromuscular or systemic disorder.
  • No use of anti-inflammatory, analgesic, or muscle-relaxant medication during the week before testing.

Exclusion Criteria:

  • Failure to attend or complete any of the three experimental sessions.
  • Performance of vigorous exercise within 24 hours before a testing session.
  • Occurrence of an adverse event that prevented adherence to or completion of the study protocol.

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: Fundamentele wetenschap
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Crossover-opdracht
  • Masker: Enkel

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: 30-Second Work / 30-Second Rest Protocol
Participants performed bilateral calf raises for 30 seconds followed by 30 seconds of rest, repeated over a total protocol duration of 5 minutes. Calf raises were performed at one repetition per second. Gastrocnemius shear-wave elastography measurements were obtained before exercise, immediately after exercise, and after the standardized 5-minute percussive therapy recovery period.
Participants performed bilateral standing calf raises for 30 seconds, followed by 30 seconds of rest. The work-rest cycle was repeated over a total protocol duration of 5 minutes. Calf raises were performed barefoot at a standardized cadence of one repetition per second using a metronome, with the feet shoulder-width apart and the hands positioned on the hips.
Experimenteel: 15-Second Work / 45-Second Rest Protocol
Participants performed bilateral calf raises for 15 seconds followed by 45 seconds of rest, repeated over a total protocol duration of 5 minutes. Calf raises were performed at one repetition per second. Gastrocnemius shear-wave elastography measurements were obtained before exercise, immediately after exercise, and after the standardized 5-minute percussive therapy recovery period.
Participants performed bilateral standing calf raises for 15 seconds, followed by 45 seconds of rest. The work-rest cycle was repeated over a total protocol duration of 5 minutes. Calf raises were performed barefoot at a standardized cadence of one repetition per second using a metronome, with the feet shoulder-width apart and the hands positioned on the hips.
Experimenteel: 45-Second Work / 15-Second Rest Protocol
Participants performed bilateral calf raises for 45 seconds followed by 15 seconds of rest, repeated over a total protocol duration of 5 minutes. Calf raises were performed at one repetition per second. Gastrocnemius shear-wave elastography measurements were obtained before exercise, immediately after exercise, and after the standardized 5-minute percussive therapy recovery period.
Participants performed bilateral standing calf raises for 45 seconds, followed by 15 seconds of rest. The work-rest cycle was repeated over a total protocol duration of 5 minutes. Calf raises were performed barefoot at a standardized cadence of one repetition per second using a metronome, with the feet shoulder-width apart and the hands positioned on the hips.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Mean Change in Medial Gastrocnemius Shear-Wave Velocity
Tijdsspanne: Baseline, immediately after each 5-minute calf-raise protocol, and after the subsequent 5-minute percussive therapy recovery period, during each of 3 sessions separated by at least 48 hours.
Medial gastrocnemius stiffness was assessed bilaterally using shear-wave elastography and reported as shear-wave velocity in meters per second (m/s), with higher values indicating greater stiffness. Three acquisitions were obtained for each leg at each time point and averaged. Mean changes were evaluated within each work-to-rest protocol from baseline to immediately after exercise, from immediately after exercise to after the percussive therapy recovery period, and from baseline to after recovery.
Baseline, immediately after each 5-minute calf-raise protocol, and after the subsequent 5-minute percussive therapy recovery period, during each of 3 sessions separated by at least 48 hours.

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)

24 juni 2025

Primaire voltooiing (Werkelijk)

24 februari 2026

Studie voltooiing (Werkelijk)

24 maart 2026

Studieregistratiedata

Eerst ingediend

30 juli 2026

Eerst ingediend dat voldeed aan de QC-criteria

30 juli 2026

Eerst geplaatst (Werkelijk)

4 augustus 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

4 augustus 2026

Laatste update ingediend die voldeed aan QC-criteria

30 juli 2026

Laatst geverifieerd

1 juli 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

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

ONBESLIST

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