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Treatment of Muscle Injuries With Physium Therapy.

Treatment of Muscle Injuries With Physium Therapy.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03762720
Acronym
Physium
Enrollment
20
Registered
2018-12-04
Start date
2019-07-15
Completion date
2019-08-15
Last updated
2019-06-20

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

Conditions

Injuries; Muscle, Nontraumatic

Keywords

Manual Therapy, Massage, physium, pain, range of motion, quality of life, muscle injuries

Brief summary

Muscle injuries are currently particularly frequent among people who participate in sports. The diagnosis is easily made with an ultrasound study and Shear Wave Elastography.

Detailed description

Patients of the experimental group, after diagnosis by ultrasound and Shear Wave Elastography , will receive five sessions of physium therapy at 80 millibars during one month. The measurements of the variables visual analog scale, joint mobility through the double inclinometer device, elasticity and tissue vascularization through the ultrasound, quality of life through SF-12 questionnaire and pressure algometry will be made before, after, month and three months after the end of treatment.

Interventions

DEVICEPhysium treatment

patients will receive five sessions of physium therapy at 80 millibars in 30 minutes for one month in muscle injury and diagnosed by ultrasound and Shear Wave Elastography.

Sponsors

University of Cadiz
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Masking description

Blind researcher

Intervention model description

RANDOMIZED CLINICAL TRIAL WITH BLIND EVALUATION BY THIRD PARTIES, LONGITUDINAL AND PROSPECTIVE.

Eligibility

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

Inclusion criteria

* Patients of both sexes, aged between 20 and 60 years, in an active state of pain and diagnosed with muscle breakdown.

Exclusion criteria

* Patients who are pregnant, have pacemakers and surgically operated in the area to be treated.

Design outcomes

Primary

MeasureTime frameDescription
Time necessary to return to full sport participation.BaselineTime necessary to return to full sport participation.

Secondary

MeasureTime frameDescription
Range of motion.Baseline and four weeksMeasured by goniometer.
The intensity of painBaseline and four weeksA 10-point Numerical Pain Rating Scale (NPRS; 0: no pain, 10: maximum pain) will be used to assess the patients' current level of pain, and the worst and lowest level of pain experienced in the preceding week in the area.
Time necessary to return to full sport participation.Four weeks.Time necessary to return to full sport participation.
Questionnaire SF 12Baseline and four weeksThe multidimensional health related quality of life
the extent of sports-related muscle injuriesBaseline and four weeksImaging is crucial to confirm and assess the extent of sports-related muscle injuries and may help to guide management.
Pressure pain thresholds in cervical trigger pointsBaseline and four weeksPressure pain thresholds (PPTs) will be measured with a pressure algometer

Contacts

Primary ContactManuel Rodriguez Huguet, Physiotherapy
manuel.rodriguez@uca.es+34606176814

Outcome results

None listed

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