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Electrical Stimulation vs. Static Stretching in the Leg Muscles

Effect of Electrical Muscle Elongation vs. Static Stretching in the Leg Muscles Contracture

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06626698
Enrollment
56
Registered
2024-10-04
Start date
2024-06-01
Completion date
2024-07-31
Last updated
2025-12-19

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

Conditions

Muscle Fatigue

Keywords

Achilles tendon, gastrocnemius muscle, electric stimulation, static stretching, articular Range of Motion, randomized Clinical trial, Longitudinal, muscle shortening, Session duration, Comparision group, Electric muscle elongation, triceps surae

Brief summary

The retraction of the posterior leg muscles consists of a shortening of the muscle fibers that limits ankle dorsiflexion. The objective of this randomized controlled clinical trial (RCT) with a double-blind technique and longitudinal chronology is to evaluate the short-term effect of electrostimulation associated with muscle stretching (electrical muscle elongation technique or EME) compared to static stretching in adult subjects with shortening of the posterior leg muscles. The main questions it seeks to answer are: * Are there significant differences in the short-term effect of electrical muscle elongation versus static stretching exercises on the gastrocnemius complex and Achilles tendon in young adults? * Does the ankle's range of motion increase in both weight-bearing and non-weight-bearing positions? * Does muscle strength increase in ankle plantar flexion? The researchers will compare the group receiving electrical muscle elongation with interferential current to the group receiving passive static stretching to assess whether there are significant differences in the effects on the ankle's range of motion and the muscle strength of the posterior leg muscles. Participants in this study will perform the following tasks: * Receive a session of electrical muscle elongation with TENS and static stretching performed by the researcher. * Follow the instructions during the intervention. * Undergo evaluations of ankle range of motion and plantar flexor muscle strength * Record their level of satisfaction after the study.

Interventions

OTHERStatic stretching

A passive static stretch of the posterior leg muscles will be performed with the subject in a supine position and knees extended, starting with the ankle at 90º and continuing until reaching the maximum tolerated dorsiflexion.

DEVICEElectrical muscle elongation

The intervention will be performed with the subject in a supine position with knees extended. Electrodes will be placed on the gastrocnemius muscles of the leg being assessed. The parameters will be selected. Static stretching will begin until resistance is felt, at which point the intensity of the electrical current will be increased to induce a visible and tolerable contraction. Simultaneously, the subject will be asked to perform an isometric contraction of the antagonist muscles, resisted by the investigator. When the subject feels the stretch again, the intensity of the current will be increased once more until a new movement barrier is reached.

Sponsors

University of Seville
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

This was a single-blind study. The Participants were blinded to the specific intervention they received, as both the Electrical Muscle Elongation (EME) technique and the Static Stretching (SS) technique involved similar positioning and physical manipulation of the ankle, making it challenging for them to distinguish the exact treatment modality. However, the Investigator (A.C-M, responsible for allocation and data recording) and the Care Provider (L.R-F, the podiatrist who applied the corresponding technique) were not blinded to the group assignment due to the distinct nature of the two interventions (one involving electrotherapy equipment and the other not).

Intervention model description

Participants were randomly assigned to either the Experimental Group (Electrical Muscle Elongation, EME) or the Control Group (Static Stretching, SS) to compare the immediate and short-term effects of the interventions.

Eligibility

Sex/Gender
ALL
Age
18 Years to 25 Years
Healthy volunteers
No

Inclusion criteria

* Subjects affiliated with or related to the University of Seville. * Those with muscular shortening of the posterior chain of the limb.

Exclusion criteria

* Subjects who engage in sports activity above the average of the sample or who follow an organized stretching program for the posterior leg muscles. * Hyperlaxity * History of musculoskeletal, neuromuscular injuries, joint disease, surgery on the lower leg, or serious illness.

Design outcomes

Primary

MeasureTime frameDescription
Evaluation of the ankle range motionThrough study completion, an average of 2 weeks.Assessment will be conducted in a prone position using a two-arm goniometer with the knee flexed and extended, as well as in a standing position with a digital inclinometer with the knee flexed and extended. Additionally, the distance from the big toe to the wall will be measured with a tape measure. This evaluation is carried , before and after a electric stimulation to compare if this measure may be different after this intervention At the beginning, during the intervention and a week later.
leg muscular forceThrough study completion, an average of 2 weeks.Assessment will be conducted with the subject in a supine position and with knees extended. The plantarflexor strength of the ankle will be measured using a portable dynamometer. Three measurements will be taken, and the average will be calculated. this measure is carried on to evaluation if the force of the posterior leg muscles may be increased At the beginning, during the intervention and a week later.

Secondary

MeasureTime frameDescription
Patient Global Impression of Improvement cuestionarieAt the end of the study, an average of 2 weeksA questionnaire indicating the global impression of improvement after the intervention will be administered at the end of the study. It is to assesment is this study it is confortable for the patient The scale has a total score from 1 to 7. A value of 1 indicates great improvement and a value of 7 indicates that the patient is very unwell.

Countries

Spain

Outcome results

None listed

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