Skip to content

Effectiveness of Dry Needling and Ischemic Compression in Sternocleidomastoid, on Cervical Motor Control in Patients With Cervical Pain.

Effectiveness of Dry Needling and Ischemic Compression in the Sternocleidomastoid, on Cervical Motor Control in Patients With Cervical Pain, Versus Placebo Technique and Ischemic Compression, Randomized Trial.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03331653
Enrollment
34
Registered
2017-11-06
Start date
2017-11-10
Completion date
2018-06-10
Last updated
2018-06-13

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

Conditions

Cervical Pain

Keywords

Cervical Pain, Motor Control, Sternocleidomastoid, Dry Needling

Brief summary

This study will compare the effect of dry needling on the active trigger point on sternocleidomastoid versus the effect of dry needling at 1.5 centimeters of active trigger point on sternocleidomastoid, both combined with ischemic compression, on cervical pain and cervical motor control short and medium term.

Interventions

OTHERDry Needling and Ischemic Compression at the Trigger Point

The intervention consist on dry needling in the active trigger point, and next, do ischemic compression in the same point.

OTHERDry Needling and Ischemic Compression at 1.5 centimeters from the Trigger Point

The intervention consist on dry needling at 1.5 centimeters from the active trigger point, and next, do ischemic compression in the same point.

Sponsors

University of Alcala
Lead SponsorOTHER

Study design

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

Masking description

Double-blind, masking the patient and the outcomes assesor. A simple randomization will be performed with Epidat software.

Intervention model description

Randomized Clinical Trial (RCT) with two groups.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Be between 18 and 65 years old * Have pain in the cervical region, which extends from the occipital to the 7th cervical vertebra. * Have an active trigger point on the sternocleidomastoid.

Exclusion criteria

* Present history of trauma in the neck. * Present cervical radiculopathy * Present a vestibular pathology * Previous surgery on the neck or shoulder area * Having a primary headache diagnosis * Have received dry needling in the neck in the previous 6 months * Present cognitive deficit. * Be pregnant * Taking anticoagulants. * Have phobia to the needles (belonephobia).

Design outcomes

Primary

MeasureTime frameDescription
Cervical PainPre-intervention, immediately post-intervention, 1 day, 1 week, 1 monthChanges in the level of Cervical Pain.
Cervical Motor ControlPre-intervention, immediately post-intervention, 1 day, 1 week, 1 monthChange in the Cervical Motor Control

Secondary

MeasureTime frameDescription
Cervical Range of MovementPre-intervention, immediately post-intervention, 1 day, 1 week, 1 monthChanges in grades of cervical movement
Coordination of superficial and deep cervical flexor musclesPre-intervention, immediately post-intervention, 1 day, 1 week, 1 monthChanges in the coordination of cervical flexor muscles
Cervical DisabilityPre-intervention,1 monthChanges in perceived cervical disability

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026