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Noninvasive Treatment of Upper Trapezius Active Trigger Points in College Students With Neck Pain

Noninvasive Treatment of Upper Trapezius Active Trigger Points in College Students With Neck Pain. A Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05265468
Enrollment
80
Registered
2022-03-03
Start date
2022-03-14
Completion date
2022-05-19
Last updated
2022-05-20

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

Conditions

Neck Pain, Trigger Point Pain, Myofascial

Keywords

Physiotherapy, Rehabilitation, Treatment, Active Trigger Point

Brief summary

Hyperexcitable myofascial trigger points located within a taut band of skeletal muscle or fascia cause referred pain, local tenderness, and autonomic changes. The scientific data refer to an immediate improvement in the symptoms of these active points treated with manual therapy. Based on these factors, the objective of the study is to determine the effect of the combined therapy of the Jones, Chaitow, Lewit technique and pain-free positioning in participants with the presence of an active upper trapezius trigger point.

Detailed description

The treatment will last a total of 15 minutes accompanied by a baseline assessment and after 10 minutes of the intervention in 3 experimental groups and a placebo group, of no-pain positioning. In addition to basic indices and scales of cervical pain and functionality, it is intended to measure flexibility, range of motion, proprioception and cognition through software with sensors of the latest technology when it comes to representing reliable results in differences between techniques.

Interventions

No pain positioning technique with diaphragmatic breathing

OTHERLewit Group

Isometric muscular exercise acompained with stretching technique

OTHERChaitow Group

Isometric muscular exercise acompained with stretching technique and diaphragmatic breathing

OTHERPlacebo Group

No pain positioning of participants

Sponsors

Universidad Católica San Antonio de Murcia
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
19 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* persistent neck pain or headache for more than 3 days * presence of active trigger point in upper trapezius

Exclusion criteria

* Participants who present dizziness, vertigo and/or symptoms aggravated by the movement and/or positioning of the neck; * who present infection or febrile state at the time of performing the test; * with anxiety and/or extreme emotional tension; * who are undergoing pharmacological treatment (analgesics, muscle relaxants, anxiolytics, antidepressants)

Design outcomes

Primary

MeasureTime frameDescription
Neck Disability Index10 minutesSelf-completed neck questionnaire wich consists in 10 sections. Each one of them (cervical pain intensity, personal care, lifting weights, reading, headache, ability to concentrate, ability to work, driving, sleep and leisure activities) offers 6 possible answers that represent 6 progressive levels of functional capacity, and is scored from 0 to 5. The total score is expressed in percentage terms with respect to the maximum possible
Pain intensity10 minutesMeasured with Numeric Rating Scale wich consist in measure pain intensity with a score of 0-10
Pression algometer10 minutesMeasures pressure pain thresholds

Secondary

MeasureTime frameDescription
Cervical Test10 minutesMeasured with Baiobit Software. The range of movement will be measured in grades as per: flexion/extension; right/left rotation; and right/left inclination
Proprioceptive Test10 minutesMeasured with Baiobit Software o'clock test in a high/medium/low levels wich consist in a velocity and accuracy evaluation of combined cervical movements in the o'clock game test.

Countries

Spain

Outcome results

None listed

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