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Immediate Effects of Shock Wave Therapy With Stretching or Isometric Contraction on Upper Trapezius (rESWT)

19 mei 2026 bijgewerkt door: Gukhwa Han, Sahmyook University

The Immediate Effects of Simultaneous Application of Radial Extracorporeal Shock Wave Therapy and Stretching or Isometric Contraction on Muscle Tone, Stiffness, Thickness, Pressure Pain Threshold, and Grip Strength of the Upper Trapezius

Excessive use of smart devices and prolonged sitting posture in modern daily life can lead to potential hypertonicity and functional impairment of the upper trapezius even in healthy individuals. Such conditions may cause functional changes and discomfort before the onset of pain, and early intervention may help prevent the progression to musculoskeletal disorders. Therefore, this study aims to investigate the immediate effects of radial extracorporeal shock wave therapy (rESWT) applied simultaneously with stretching or isometric contraction on muscle tone, stiffness, thickness, pressure pain threshold, and grip strength of the upper trapezius in healthy adults.

Participants will be divided into two groups : rESWT + stretching and rESWT + isometric contraction. Immediate changes in the upper trapezius will be compared before and after the interventions. rESWT will be applied to the upper trapezius with 1.0 bar pressure, 10 Hz frequency, and 1000 shocks.

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

      • Gwangju, Zuid -Korea, 62287
        • 73, Bungmun-daero 419beon-gil, Gwangju health university

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:

  • Individuals with no history of neck or shoulder pain in the past 6 months
  • Individuals with no history of upper limb musculoskeletal disorders
  • Individuals with a pressure pain threshold (PPT) of the upper trapezius ≥ 263 kPa

Exclusion Criteria:

  • Individuals with a history of neurological or orthopedic disorders
  • Individuals taking medications that may affect ESWT response
  • Individuals with local skin conditions, including ulcers or open wounds

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
Actieve vergelijker: experimental 1 group
Radial Extracorporeal Shock Wave Therapy and Stretching

Participants will sit on a chair and receive rESWT with gel applied to the upper trapezius. A 20 mm rESWT applicator angled at 90° will be applied to the muscle belly and the musculotendinous junction. The intensity will be set at 1.0 bar pressure, 10 Hz frequency, with 1000 shocks.

When rESWT is applied to the upper trapezius, participants will sit on a chair and repeatedly bend the neck diagonally to stretch the muscle, then return to the neutral position.

Actieve vergelijker: experimental 2 group
Radial Extracorporeal Shock Wave Therapy and Isometric Contraction

Participants will sit on a chair and receive rESWT with gel applied to the upper trapezius. A 20 mm rESWT applicator angled at 90° will be applied to the muscle belly and the musculotendinous junction. The intensity will be set at 1.0 bar pressure, 10 Hz frequency, with 1000 shocks.

When rESWT is applied to the upper trapezius, participants will sit on a chair and maintain a shoulder elevation posture during the intervention.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Muscle Tone
Tijdsspanne: Post-intervention measurement is conducted immediately after the intervention to assess immediate effects.
Upper trapezius muscle stiffness will be assessed as dynamic stiffness (N/m) using the MyotonPRO device (Myoton AS, Tallinn, Estonia). The probe will be positioned perpendicular to the skin over the belly of the upper trapezius muscle. After a pre-load of approximately 0.18 N, 10 mechanical impulses of approximately 0.4 N at 1 Hz will be delivered. Measurements will be repeated 3 times, and the mean value will be used for analysis. Change from baseline will be calculated as the immediate post-intervention value minus the baseline value.
Post-intervention measurement is conducted immediately after the intervention to assess immediate effects.
Muscle Stiffnes
Tijdsspanne: Post-intervention measurement is conducted immediately after the intervention to assess immediate effects.
Upper trapezius muscle stiffness will be assessed as dynamic stiffness (N/m) using the MyotonPRO device (Myoton AS, Tallinn, Estonia). The probe will be positioned perpendicular to the skin over the belly of the upper trapezius muscle. After a pre-load of approximately 0.18 N, 10 mechanical impulses of approximately 0.4 N at 1 Hz will be delivered. Measurements will be repeated 3 times, and the mean value will be used for analysis. Change from baseline will be calculated as the immediate post-intervention value minus the baseline value.
Post-intervention measurement is conducted immediately after the intervention to assess immediate effects.
Muscle Thickness
Tijdsspanne: Post-intervention measurement is conducted immediately after the intervention to assess immediate effects.
The probe of the ultrasound imaging device is placed perpendicular to the target area without applying any pressure after applying a water-based transmission gel, in order to measure muscle thickness. Then, using a 2.5 MHz ultrasound, strong echoes at tissue interfaces are focused, and the distance between the focused points is converted into millimeters to determine tissue thickness.
Post-intervention measurement is conducted immediately after the intervention to assess immediate effects.
Grip Strength
Tijdsspanne: Post-intervention measurement is conducted immediately after the intervention to assess immediate effects.
Grip strength is measured using a wireless dynamometer. The participant holds the dynamometer with the arm relaxed, the elbow flexed at 90°, the arm slightly away from the torso, and the wrist in a neutral position. Following the researcher's instructions, the participant exerts maximum force. The measurement is repeated three times, and the average value is recorded.
Post-intervention measurement is conducted immediately after the intervention to assess immediate effects.
Pressure Pain
Tijdsspanne: Post-intervention measurement is conducted immediately after the intervention to assess immediate effects.
The participant sits upright with the back supported by a wall or chair and feet flat on the floor. A pressure algometer with a 1 cm² rubber tip is placed perpendicular to the same muscle belly measured by the Myoton PRO. The researcher applies gradual pressure at a constant rate of 0.5 kg/cm²/s until the participant reports pain, and the value at the point of reported pain is recorded. The measurement is repeated twice, and the average value is used.
Post-intervention measurement is conducted immediately after the intervention to assess immediate effects.

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)

20 september 2025

Primaire voltooiing (Werkelijk)

10 oktober 2025

Studie voltooiing (Werkelijk)

25 oktober 2025

Studieregistratiedata

Eerst ingediend

11 december 2025

Eerst ingediend dat voldeed aan de QC-criteria

19 mei 2026

Eerst geplaatst (Werkelijk)

27 mei 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

27 mei 2026

Laatste update ingediend die voldeed aan QC-criteria

19 mei 2026

Laatst geverifieerd

1 mei 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

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

NEE

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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