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Effects of Dry Needling on the Behavior of the Shoulder Muscles

Effect of Dry Needling Technique on Shoulder Muscle Functionality in Subjects With and Without Shoulder Pain.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06398574
Enrollment
40
Registered
2024-05-03
Start date
2024-05-06
Completion date
2026-12-20
Last updated
2026-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Shoulder Pain

Keywords

Dry needling, Shoulder muscle strength, Surface electromyography

Brief summary

The main objective of this study will be to evaluate the effects of the application of the dry needling technique on the activity of the rotator cuff muscles in the shoulder. The evaluation of the effects of the application of the dry needling technique will be carried out in subjects with and without shoulder pain.To do this, muscle strength, possible thickness changes in the muscle and electromyographic activity will be measured before and immediately after the application of a dry needling technique. Likewise, other variables will be measured such as the pressure pain threshold (PPT), pain with a Numeric Verbal Scale, kinesiophobia and catastrophism, the shoulder pain and disability index (SPADI) and the influence of expectations about dry needling.

Interventions

With the subject lying supine, a dry needling technique will be applied to the infraspinatus muscle. First, the most hyperalgesic point in the muscle will be located. Subsequently, Hong's fast-in and fast-out technique will be applied. Ten incisions will be made

OTHERSham dry needling

With the subject lying supine, a sham dry needling technique will be applied to the infraspinatus muscle. First, the most hyperalgesic point in the muscle will be located. Subsequently, Hong's fast-in and fast-out technique will be applied. Ten incisions will be made, simulating the real technique

Sponsors

University of Alcala
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Subjects of legal age * Subjects without shoulder pain or with unilateral shoulder pain of \> 3 months duration. * Have shoulder mobility of 90º of abduction and at least 30º of glenohumeral external rotation.

Exclusion criteria

* Have neck pain. * Whiplash * Having had trauma to the shoulder. * Having fibromyalgia. * Be pregnant. * Being afraid of needles.

Design outcomes

Primary

MeasureTime frameDescription
Muscle strengthChange from Baseline at 15 minutes.The isometric strength will be assessed using a handheld dynamometer (Hand held dynamometer, MicroFET3; Hoggan Health Industries Inc.). The strength measures will included external rotation at 90° abduction in the prone position. The dynamometer will be placed just proximal to the just proximal to the styloid process of the wrist joint. Subjects will be asked to produce a 5-second maximal contraction. Muscular strength will be measured in kilograms

Secondary

MeasureTime frameDescription
Muscle functionChange from Baseline at 15 minutes.Muscle function will be measured by an ultrasound scanner with a linear transducer with a frequency range of 6-16MHz (X6-16L, 5cm footprint) will be used. The unit of measurement used will be millimeters. Muscle thickness at rest and contraction will be measured. On the other hand, the percentage of change in thickness will be measured using the equation (Contraction thickness - Rest thickness) \* 100 / Rest thickness.
Shoulder PainChange from Baseline at 15 minutes.Pain intensity will be measured using the Visual Analog Scale (VAS) for pain. The VAS is a 100-mm line, oriented horizontally, with one end representing "no pain" and ten the other end representing "worst pain." Subjects will be asked to rate their current pain with a mark on the scale.
DisabilityChange from Baseline at 15 minutes.Disability will be measured by Shoulder Pain and Disability Index (SPADI).The Spanish version of SPADI has high test-retest reliability (ICC 0.89-0.93).The clinically important minimum difference varies between 8 and 13.2. The minimum value is 0 and de maximum value is 100
Pressure Pain Threshold (PPT)Change from Baseline at 15 minutes.An algometer Wagner FPI 10-WA will be used to determine the PPT in infraespinatus muscle.

Countries

Spain

Contacts

CONTACTMarina Ortega-Santamaria, PhD student
marinaortegasantamaria@gmail.com(+34) 683 378 391
CONTACTCentro Investigacion Fisioterapia y Dolor
STUDY_CHAIRDaniel Pecos-Martin, PhD

Alcala University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 2, 2026