Muscle Position and Dry Needling Efficacy
The Importance of Muscle Position in the Effectiveness of Dry Needling Technique
Currently, no previous studies have investigated how the position of a muscle before dry needling may influence the outcome and effectiveness of the treatment.
This study aims to demonstrate whether the position of the upper trapezius muscle during dry needling treatment influences the outcome of that treatment in subjects with neck pain.
A total of 46 participants with chronic neck pain will be recruited and randomly assigned to two groups: a dry needling group with the muscle in a stretched position and a dry needling group with the muscle in a shortened position. A total of two treatment sessions will be performed, separated by a 7-day interval. The primary outcome measure will be the intensity of neck and head pain, measured using the visual analog scale (VAS). Other variables to be measured include the cervical disability index, kinesiophobia, and catastrophizing (using a self-completion questionnaire), as well as participants' expectations and post-needling pain.
Descripción general del estudio
Estado
Condiciones
Tipo de estudio
Inscripción (Estimado)
Fase
- No aplica
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Daniel Pecos-Martin, PhD
- Número de teléfono: 34918855142
- Correo electrónico: daniel.pecos@uah.es
Ubicaciones de estudio
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Madrid
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Alcalá de Henares, Madrid, España, 28805
- Reclutamiento
- Physioterapy and Pain center research
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Contacto:
- Laura López Pérez, Mrs
- Número de teléfono: +34683378391
- Correo electrónico: info@institutofisioterapiaydolor.es
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Alcalá de Henares, Madrid, España, 2805
- Reclutamiento
- Clinical University Physiotherapy and pain
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Contacto:
- Patricia Martinez-Merinero, PhD
- Número de teléfono: 683378391
- Correo electrónico: clinica.fisio@fgua.es
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Age between 18 and 65 years
- Neck pain lasting more than 3 months
- Current neck pain greater than 3/10 on the VAS (Visual Analog Scale)
- Presence of active trigger points in the upper trapezius muscle, meeting the following criteria: Painful point within a taut band whose palpation reproduces the patient's symptoms.
Exclusion Criteria:
- Neck pain with a medical diagnosis (fractures, arthritis, fibromyalgia, etc.)
- Radicular pain (paresthesia, burning, electric shocks)
- Whiplash or any recent trauma
- Previous surgery
- Treatment by another physiotherapist within the last 3 months
- Infections
- Needle phobia
- Use of anticoagulant medications
- Pregnancy
- Fibromyalgia
- Metal allergies
- Cognitive deficits or communication problems
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Doble
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Experimental: Upper trapezius dry needling with adduction shoulder
The dry needling technique will be applied to the trapezius muscle while the subject lies prone, with the upper limb at the side of the body, shoulder lowered, in adduction and cervical region in a neutral position. The dry needling technique will be applied using a pincer grasp, inserting the needle from the posterior to the anterior portion of the upper trapezius muscle. |
Ten incisions will be made in a posteroanterior direction while the patient lies prone and the muscle is grasped with a pincer grip between the first three fingers.
The technique will be applied to the area that is mechanically most hyperalgesic and related to the reproduction of the patient's pain.
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Experimental: Upper trapezius dry needling with 90º abduction shoulder
The dry needling technique will be applied to the trapezius muscle while the subject lies prone, with the upper limb separated from the body, shoulder at 90 degrees of abduction and cervical region in a neutral position. The dry needling technique will be applied using a pincer grasp, inserting the needle from the posterior to the anterior portion of the upper trapezius muscle. |
Ten incisions will be made in a posteroanterior direction while the patient lies prone and the muscle is grasped with a pincer grip between the first three fingers.
The technique will be applied to the area that is mechanically most hyperalgesic and related to the reproduction of the patient's pain.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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The visual analog scale (VAS)
Periodo de tiempo: Change from baseline at 3 months
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Intensity of neck and head pain: This was measured using the visual analog scale (VAS).
It consists of a 10 cm horizontal line, where 0 cm on the left side represents "no pain" and 10 cm on the right side represents "maximum pain."
The subject marks a perpendicular line at the point they consider to represent their pain intensity.
The examiner then places a millimeter ruler on the scale, assigning a numerical value to the line drawn by the patient.
The VAS has proven to be a valid and reliable tool (intraclass correlation coefficient [ICC] 0.71-0.99).
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Change from baseline at 3 months
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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Disability Associated with Neck Pain
Periodo de tiempo: Change from baseline at 3 months
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The degree of disability associated with neck pain will be measured using the Neck Disability Index (NDI) questionnaire in its Spanish version.
The NDI is a 10-item questionnaire, and each item is scored on a scale of 0 to 5 points, with a range of 0 to 50 points.
The higher the score, the greater the degree of disability.
The NDI has proven to be a reliable tool (ICC 0.98).
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Change from baseline at 3 months
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Kinesiophobia with the Tampa Kinesiophobia Scale (TSK-11)
Periodo de tiempo: Change from baseline at 3 months
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The Tampa Kinesiophobia Scale (TSK-11) short version will be used to assess fear of movement.
It is an 11-item scale rated on a four-point scale ranging from "strongly agree" to "strongly disagree."
Scores range from 11 to 44, with higher scores indicating greater fear of movement and/or (re)injury.
This questionnaire has demonstrated similar properties to the original TSK scale, proving to be a valid and reliable instrument.
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Change from baseline at 3 months
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Catastrophizing with the Pain Catastrophizing Scale (PCS)
Periodo de tiempo: Change from baseline at 3 months
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Catastrophizing Scale (PCS).
The PCS has 13 items scored from 0 to 4 and is composed of three subscales: rumination, magnification, and helplessness.
The overall score ranges from 0 to 52.
Higher scores indicate a greater degree of pain catastrophizing.
A total score >30 represents a clinically significant level of pain catastrophizing.
This questionnaire has been shown to be reliable (ICC 0.94).
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Change from baseline at 3 months
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Local twitch response (LTRs)
Periodo de tiempo: Change from baseline at 3 months
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Local twitch response (LTRs).
The LTRs produced by needle insertion during dry needling will be counted.
LTRs are generally associated with better treatment outcomes.
A higher number of LTRs indicates better results, and a lower number of LTRs indicates worse results.
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Change from baseline at 3 months
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Cervical joint Range
Periodo de tiempo: Change from baseline mobility at one week after intervention
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Flexion, inclination, extension and rotational movement ranges will be measured with a cervical goniometer
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Change from baseline mobility at one week after intervention
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Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- CEEI22/199
Plan de datos de participantes individuales (IPD)
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Información sobre medicamentos y dispositivos, documentos del estudio
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