- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07562360
The Effectiveness of Tecar Therapy in Management of Calf Muscle Strain Injuries (MS)
April 25, 2026 updated by: Nabil Mahmoud Ismail Abdel-Aal, Cairo University
this study will be conducted to investigate the effect of TECAR Therapy on quality of landing, healing and Function in patient with Calf Muscle Strain.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Calf muscle strain is one of the most common muscle injuries in high-performance athletes and contributes to substantial player downtime because of its high mean time to return to sport and occurrence during critical periods in the competitive season.
Published reports on lower-body muscle strain have provided frequent updates on the rehabilitation of high-profile muscle groups, such as the hamstring muscles, and improvements to calf strain management are seldom discussed despite the prevalence of these injuries in competitive sports.
In this article, we discuss the diagnosis, treatment, outcomes, risk factors, and prevention of calf muscle strain in athletes.Transfer of Electricity-Capacitive and Resistive (Tecar) therapy is considered a special form of energy that uses frequencies between 300 KHz and 1 MHz and is characterized as a non-invasive high-frequency energy that awakens the body's natural ability to self-regenerate.
Thus, it promotes the natural physiological processes of the tissue metabolically, transferring energy without introducing radiation from the external environment.
TECAR therapy stands out as a promising yet underexplored modality.
Its mechanism of action-utilizing both capacitive and resistive energy transfer-suggests a novel approach to addressing musculoskeletal injuries and pain.
While preliminary studies and clinical applications hint at its potential advantages, such as improved tissue healing and pain relief, a comprehensive evaluation of the existing research is necessary to fully understand the role of TECAR therapy in rehabilitation
Study Type
Interventional
Enrollment (Estimated)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Nabil Abdel-Aal, professor
- Phone Number: 01200133613
- Email: nabil.mahmoud@cu.edu.eg
Study Contact Backup
- Name: Hossam Mostafa, master
- Phone Number: 01092727746
- Email: h.elshatory@gmail.com
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Aged between 16-39 years of age.
- not having suffered leg injuries in the past 6 months.
- not having suffered a triceps sural rupture in the past two years.
- be diagnosed with latent MTPs in the gastric-soleus complex through manual therapy in the dominant side.
- Presence of Calf muscles Strain evaluated by Ultrasonography.
- Athlete willing and able to participate in an exercise program safely.
- The radiologist also assessed whether the tendon ends could be reduced in passive plantar flexion of the ankle joint with the knee extended.
- Athlete BMI from 18.5 to 24.9 kg / m2
Exclusion Criteria:
- connective tissue pathology.
- lymphatic disorders (lymphadenopathy).
- Skin injuries (open wounds, infection, psoriasis, tattoos, hematoma).
- peripheral neuropathies.
- previous fractures.
- previous lower limb surgeries (in the past 12 months).
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: TECAR therapy
Thirty patients will receive TECAR therapy combined with conventional treatment three times per week for 12 weeks.
|
The TECAR intervention was administered to the calf muscle using the Zimmer devicein capacitive (CAP) mode for a duration of 20 min.
The therapy was applied with the signal at a variable power with a maximum of 300 W. The frequency used was 500 kHz with an intensity of 40%.
The intervention was standardized to a distal-to-proximal stroking rhythm with moderate pressure.
For the TECAR intervention, the capacitive (CAP) mode at 500 kHz with 40% intensity and a maximum power of 300 W was chosen to optimize deep tissue heating and promote local blood flow and tissue recovery.
The 20 min duration reflects protocols commonly used in therapeutic settings for muscle recovery and rehabilitation plus conventional therapy
the patients will receive stretching exercises of the gastrocnemius (straight leg) and soleus (bended knee), eccentric exercises for calf muscles, plus plyometric exercises.
|
|
Active Comparator: conventional treatment
Thirty patients will receive conventional treatment three times per week for 12 weeks.
|
the patients will receive stretching exercises of the gastrocnemius (straight leg) and soleus (bended knee), eccentric exercises for calf muscles, plus plyometric exercises.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
size of injury
Time Frame: up to 12 weeks
|
ultrasonography device will be used to assess size of injury
|
up to 12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
landing error score system
Time Frame: up to 12 weeks
|
Landing Error Scoring System is a clinical tool used to assess jump-landing mechanics for the video from my jumb land aplication .
the feet, ankle, knees, hip, trunk, shoulder, neck and head posture is assessed through the video.
it is a 17-item .
According to the performance sheet, the questions 1-15 are Yes/No questions that are rated as 0 or 1.
The questions 16 are rated as 0, 1, and 2; 0 = soft, 1= average and 2= stiff.
the question 17 are rated as 0,1,2; 0= excellent,1 average and 2= poor, so the total score ranges from zero to 19.
A higher score indicates poor technique in landing from a jump; a lower score indicates better jump-landing technique.
the score are categorized as excellent which less than 4, good score more than four and less than or equal 5, moderate score less than four and poor more than six
|
up to 12 weeks
|
|
jump height
Time Frame: up to 12 weeks
|
The vertical jump test was performed as a one-legged counter movement jump (CMJ).
Starting position was in an upright position with the hands placed behind the back.
The subjects quickly bent the knee as much as desired and then immediately jumped upward attempting to maximize the height jumped.
The subjects performed three maximal approved trials for each leg, starting with the right and alternating between the right and the left leg.
However, if the subject increased hop performance in all three jumps, additional jumps were performed until no increase was seen.
The best jump height for each leg was used for data analysis.
|
up to 12 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
May 1, 2026
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
December 1, 2026
Study Registration Dates
First Submitted
April 25, 2026
First Submitted That Met QC Criteria
April 25, 2026
First Posted (Actual)
May 1, 2026
Study Record Updates
Last Update Posted (Actual)
May 1, 2026
Last Update Submitted That Met QC Criteria
April 25, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC/012/006406
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Muscle Strain
-
Universidad Católica San Antonio de MurciaNot yet recruitingMuscle Strain | Electromyography | Trapezius Muscle Strain
-
Józef Piłsudski University of Physical EducationActive, not recruitingBalanced | Psychomotor Status | Muscle Strain, Lower Leg | Muscle Strain BackPoland
-
Cairo UniversityNot yet recruitingHamstring Muscle StrainEgypt
-
Superior UniversityActive, not recruitingTrapezius Muscle StrainPakistan
-
University of Mogi das CruzesCompleted
-
University of Erlangen-Nürnberg Medical SchoolCompleted
-
Bispebjerg HospitalUniversity of CopenhagenCompleted
-
Superior UniversityActive, not recruitingMuscle StrainPakistan
-
Aya Mohamed ElsheikhFaculty of Physical Therapy, Cairo University, Egypt is not a recognized...CompletedGroin Pain | Adductor Muscle StrainEgypt
-
American Medical AssociationAttorney General Consumer & Prescriber Education GrantCompleted
Clinical Trials on TECAR therapy
-
Ankara City Hospital BilkentRecruiting
-
Delta University for Science and TechnologyNot yet recruiting
-
Middle East UniversityNot yet recruiting
-
Universitat Internacional de CatalunyaCompletedSpasticity, Muscle | Stroke Sequelae | Massage | ElectrotherapySpain
-
Izmir City HospitalNot yet recruiting
-
Kirsehir Ahi Evran UniversitesiNot yet recruiting
-
International Hellenic UniversityCompleted
-
CAPENERGY MEDICAL, SLUniversity of Malaga; Alfonso X El Sabio UniversityCompletedObesity; Endocrine | Obesity, VisceralSpain
-
Ankara City Hospital BilkentCompletedCarpal Tunnel Syndrome | Energy Transfer Capacitative and Resistive TherapyTurkey
-
Fundación Universidad Católica de Valencia San...CompletedSports Physical Therapy | Thermography | Strain of Gastrocnemius Muscle (Diagnosis) | Diathermy Plate BurnSpain