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Kinesio Taping for Upper Trapezius Myofascial Trigger Points

24 agosto 2026 aggiornato da: Alev Atıgan, Pamukkale University

Effects of Kinesio Taping on Pain, Pressure Pain Threshold, Trapezius Muscle Thickness, and Strain Elastography in Patients With Upper Trapezius Myofascial Trigger Points: A Randomized Sham-Controlled Trial

Myofascial pain syndrome is one of the most common causes of musculoskeletal pain, and the upper trapezius is the muscle most frequently affected in the neck and shoulder region. Kinesio taping is a non-invasive, painless and low-cost method that is increasingly used in the treatment of myofascial trigger points, but its true therapeutic effect beyond placebo has not been clearly established.

The purpose of this randomized, sham-controlled trial is to evaluate the effectiveness of kinesio taping applied with the muscle inhibition technique on myofascial trigger points of the upper trapezius muscle. Forty patients with an active myofascial trigger point in the upper trapezius will be randomly assigned in a 1:1 ratio to receive either therapeutic kinesio taping or sham taping (20 patients per group). Both groups will receive four applications over two weeks (twice weekly). The primary outcome is the pressure pain threshold measured with a digital algometer. Secondary outcomes are pain intensity, trapezius muscle thickness measured by B-mode ultrasonography, and muscle stiffness assessed by strain elastography. All outcomes are assessed at baseline, on day 3, and at the end of the two-week treatment period.

Panoramica dello studio

Descrizione dettagliata

Myofascial pain syndrome is characterized by hyperirritable nodules located within taut bands of skeletal muscle, known as myofascial trigger points. The upper trapezius is the most commonly involved muscle in the neck and shoulder girdle, and trigger points in this region are an important cause of neck pain, restricted mobility and loss of productivity.

Kinesio taping has become increasingly popular in the management of myofascial trigger points because it is non-invasive, painless, inexpensive and has few adverse effects. Systematic reviews and meta-analyses suggest that kinesio taping reduces pain intensity and improves pressure pain threshold and range of motion in myofascial pain syndrome. However, the taping techniques used across studies differ substantially. Two techniques predominate: the space correction technique, in which strips are applied over the trigger point in a star-shaped pattern, and the muscle inhibition technique, in which a single I-strip is applied along the muscle fibres from insertion to origin with low tension. A trial directly comparing these two techniques found no significant difference between them, whereas a sham-controlled trial found that the space correction technique was not superior to sham at 72 hours. Studies using the inhibition technique have reported significant improvements in pressure pain threshold. Because the inhibition technique is mechanistically aimed at reducing muscle tone and is supported by stronger evidence, it was selected for this trial.

In addition, outcome measures in previous studies have been largely subjective. Pressure algometry provides a quantitative measure of the mechanical sensitivity of the trigger point, while B-mode ultrasonography allows measurement of muscle thickness and ultrasound elastography allows objective assessment of tissue stiffness. Strain elastography with calculation of the strain ratio has shown good reliability in patients with upper trapezius myofascial pain syndrome and can differentiate active trigger points, latent trigger points and control sites.

To the best of our knowledge, no sham-controlled randomized trial has evaluated kinesio taping of upper trapezius myofascial trigger points using pressure pain threshold as the primary outcome together with muscle thickness and strain elastography as objective secondary outcomes. A sham-controlled design was chosen because sham taping alone may produce a substantial placebo response, and only a sham comparator can isolate the true therapeutic effect.

In the intervention group, a single I-shaped kinesio tape strip will be applied from insertion to origin along the upper trapezius with 15-25% tension while the muscle is held in a stretched position. In the sham group, an identical tape of the same brand, colour and size will be applied to the same region without therapeutic tension and with the neck in a neutral position, so that the skin convolutions responsible for the therapeutic effect are not produced. Both groups will receive four applications over two weeks (twice weekly); at each session the existing tape is removed and a new tape applied, so the tape remains on the skin continuously throughout the treatment period.

Patients will be randomly allocated in a 1:1 ratio using a computer-generated random number list. The study is single-blind: the practitioner applying the tape cannot be blinded due to the nature of the intervention and therefore takes no part in any assessment. All pain, pressure pain threshold and ultrasonographic measurements will be performed by a researcher blinded to group allocation, after tape removal.

Tipo di studio

Interventistico

Iscrizione (Stimato)

40

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

      • Denizli, Turchia (Türkiye)
        • Pamukkale University, Faculty of Medicine, Department of Physical Medicine and Rehabilitation

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  • Age between 18 and 65 years
  • At least one active myofascial trigger point in the upper trapezius muscle diagnosed on clinical examination according to the criteria of Travell and Simons
  • Neck and/or shoulder pain lasting at least 3 months
  • Able to understand the procedures, benefits and possible adverse effects
  • Able to provide written informed consent

Exclusion Criteria:

  • Diagnosis of fibromyalgia syndrome
  • Cervical disc herniation, radiculopathy or myelopathy
  • History of cervical or shoulder surgery
  • History of trauma, fracture or structural deformity of the neck region
  • Inflammatory rheumatic disease, malignancy or serious systemic disease
  • Neurological disease or peripheral neuropathy
  • Kinesio taping to the trigger point, injection, dry needling or physical therapy to the neck region within the previous 6 months
  • Use of analgesics, muscle relaxants or non-steroidal anti-inflammatory drugs within the previous week
  • Active skin lesion, wound, dermatological disease or known allergy to tape at the application site
  • Pregnancy or lactation

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Kinesio Taping
Therapeutic kinesio taping applied to the myofascial trigger point of the upper trapezius using the muscle inhibition technique. A single I-shaped strip is applied from insertion to origin along the muscle fibres with 15-25% tension while the muscle is held in a stretched position (shoulder depressed, neck in contralateral lateral flexion and rotation). Four applications over two weeks (twice weekly).
Elastic therapeutic tape applied over the upper trapezius myofascial trigger point using the muscle inhibition technique. A single I-shaped strip is applied from insertion to origin along the muscle fibres with 15-25% tension while the muscle is held in a stretched position. The tape is renewed at each session and remains on the skin continuously throughout the two-week treatment period (four applications, twice weekly).
Comparatore fittizio: Sham Kinesio Taping
Sham taping using tape of identical brand, colour and size, applied by the same practitioner to the same anatomical region, with no therapeutic tension (0% tension) and with the neck in a neutral position, so that no skin convolutions are produced. Four applications over two weeks (twice weekly), identical in frequency and duration to the intervention group.
Tape of identical brand, colour and size applied over the same anatomical region without therapeutic tension (0% tension) and with the neck in a neutral position, so that the skin convolutions responsible for the therapeutic effect are not produced. The tape is renewed at each session and remains on the skin continuously throughout the two-week treatment period (four applications, twice weekly).

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in Pressure Pain Threshold (PPT) of the upper trapezius trigger point
Lasso di tempo: Baseline, day 3, and end of week 2
Pressure pain threshold measured over the marked trigger point with a digital algometer with the participant prone and the muscle relaxed. The probe is applied perpendicular to the trigger point and pressure is increased at approximately 1 kg/cm2/s. The participant reports verbally when the pressure first becomes painful. The mean of three measurements taken at least 30 seconds apart is used. An increase indicates reduced trigger point sensitivity.
Baseline, day 3, and end of week 2

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in pain intensity measured by Visual Analogue Scale (VAS)
Lasso di tempo: Baseline, day 3, and end of week 2
Pain intensity assessed on a 10 cm horizontal visual analogue scale anchored at 0 (no pain) and 10 (unbearable pain). The marked distance is measured with a ruler.
Baseline, day 3, and end of week 2
Change in upper trapezius muscle thickness measured by B-mode ultrasonography
Lasso di tempo: Baseline, day 3, and end of week 2
Muscle thickness measured with a diagnostic ultrasound device using an 8-13 MHz linear probe placed parallel to the muscle fibres over the marked region. On a clear longitudinal image of the upper trapezius, the shortest vertical distance between the superior and inferior hyperechoic borders of the muscle at the centre of the image is recorded.
Baseline, day 3, and end of week 2
Change in muscle stiffness measured by strain elastography (strain ratio)
Lasso di tempo: Baseline, day 3, and end of week 2
Strain elastography performed with the participant prone and the probe parallel to the muscle fibres at the midpoint between the C7 spinous process and the acromion. Constant light probe pressure is maintained using the pressure feedback indicator. Two regions of interest are placed: a reference region in subcutaneous fat (approximately 2x5 mm) and a target region over the trigger point (approximately 3x8 mm). The strain ratio is calculated as the muscle region value divided by the fat region value and is inversely related to tissue stiffness. The mean of three measurements recorded at end-expiration is used.
Baseline, day 3, and end of week 2

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Alev ATIGAN, Assistant Professor, Pamukkale University

Pubblicazioni e link utili

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Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 agosto 2026

Completamento primario (Stimato)

1 ottobre 2026

Completamento dello studio (Stimato)

1 ottobre 2026

Date di iscrizione allo studio

Primo inviato

24 agosto 2026

Primo inviato che soddisfa i criteri di controllo qualità

24 agosto 2026

Primo Inserito (Effettivo)

27 agosto 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

27 agosto 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

24 agosto 2026

Ultimo verificato

1 agosto 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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