European University Cyprus
Nicosia, 2404, Cyprus
NCT Number: NCT05187468
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.
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Notify Me18 year–65 year
All sexes
Interventional
Not applicable
Nicosia, 2404, Cyprus
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
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
1000 pulses at 60 mj, 10 Hz
Other names: ESWT, rSWT
Ultrasound therapy 5 min, 1,2W/cm2, 10 min Massage, 10 min heat pack
Time frame: baseline
Visual Analogue Scale 1-10 (1 is the least pain, 10 is the worst pain)
Time frame: one week
Visual Analogue Scale 1-10 (1 is the least pain, 10 is the worst pain)
Time frame: two weeks
Visual Analogue Scale 1-10 (1 is the least pain, 10 is the worst pain)
Time frame: three weeks
Visual Analogue Scale 1-10 (1 is the least pain, 10 is the worst pain)
Time frame: 1 month after
Visual Analogue Scale 1-10 (1 is the least pain, 10 is the worst pain)
Time frame: baseline
Pain tolerance to compression. Measured in kilos
Time frame: one week
Pain tolerance to compression. Measured in kilos
Time frame: two weeks
Pain tolerance to compression. Measured in kilos
Time frame: three weeks
Pain tolerance to compression. Measured in kilos
Time frame: one month after
Pain tolerance to compression. Measured in kilos
Time frame: baseline
Goniometer (measured in degrees)
Time frame: one week
Goniometer (measured in degrees)
Time frame: two weeks
Goniometer (measured in degrees)
Time frame: three weeks
Goniometer (measured in degrees)
Time frame: one month after
Goniometer (measured in degrees)
Time frame: baseline
functionality of Neck related to pain for daily activities. measured in % (36 questions). Higher the %, greater the disability
Time frame: one week
functionality of Neck related to pain for daily activities. measured in % (36 questions). Higher the %, greater the disability
Time frame: two weeks
functionality of Neck related to pain for daily activities. measured in % (36 questions). Higher the %, greater the disability
Time frame: three weeks
functionality of Neck related to pain for daily activities. measured in % (36 questions). Higher the %, greater the disability
Time frame: one month after
functionality of Neck related to pain for daily activities. measured in % (36 questions). Higher the %, greater the disability
European University Cyprus
Other
The Effectiveness of Radial Extracorporeal Shockwave on Upper Trapezius Myofascial Trigger Points
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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