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The Effectiveness of Radial ESWT on Upper Trapezius Mtrps

The Effectiveness of Radial Extracorporeal Shockwave on Upper Trapezius Myofascial Trigger Points

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05187468
Enrollment
56
Registered
2022-01-11
Start date
2019-08-01
Completion date
2020-02-28
Last updated
2022-01-11

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

Conditions

Myofascial Pain Syndrome, Myofascial Trigger Point Pain, Upper Trapezius Trigger Points

Keywords

Myofascial Trigger points, upper trapezius, Myofascial pain syndrome, Mtrps

Brief summary

This study looked after the effectiveness of radial ESWT on upper trapezius mtrps. There were three intervention groups which recieved either ESWT or standard care. VAS, PPT, Neck ROM and Cervical functionality were the main outcomes.

Detailed description

This study was a randomized controlled trial consisted of three intervention groups. Two of them recieved ESWT with different parameters in each group, while the third one was standard care recieving Ultrasound therapy, Therapeutic massage and Heat packs Participants were divided randomly into the three groups. Participants were blind to the group allocated and also the therapist and outcome investigator were blind. The participants recieved three weekly sessions. The evaluation took place before therapy, after each session and one month after last session. The outcome measures was the pain intensity with VAS, the pain tolerance to pressure by an algometer device, the range of motion of neck measured by electronic goniometer and and functionality of neck measured by the Northwick Park Neck Pain

Interventions

DEVICEExtracorporeal Shockwave Therapy

1000 pulses at 60 mj, 10 Hz

DEVICEUltrasound therapy, Massage, Heat pack

Ultrasound therapy 5 min, 1,2W/cm2, 10 min Massage, 10 min heat pack

Sponsors

European University Cyprus
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Pain between shoulder and neck on upper trapezius muscle * Three out of five of Travel and Simons criteria for myofascial trigger points

Exclusion criteria

* Fibromyalgia diagnosis * Systemic diseases diagnosis, * Pacemaker, under 18, * Any kind of cervical disorder or surgery, * Mental disorders

Design outcomes

Primary

MeasureTime frameDescription
Pain intensity on myofascial trigger pointsbaselineVisual Analogue Scale 1-10 (1 is the least pain, 10 is the worst pain)
Pressure Pain ThresholdbaselinePain tolerance to compression. Measured in kilos
cervical range of motionbaselineGoniometer (measured in degrees)
Northwick Park Neck Pain questionnairebaselinefunctionality of Neck related to pain for daily activities. measured in % (36 questions). Higher the %, greater the disability

Countries

Cyprus

Outcome results

None listed

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