ClinicalTrials.gg
RecruitingNCT07492732Updated Mar 25, 2026

Comparison of the Effects of Selected Training Methods and SIS Stimulation on Balance, Motor Tests, and Strength

An observational study in Hamstring Injury, sponsored by Gdansk University of Physical Education and Sport. Recruiting at 1 site in Poland. Open to participants aged 19 Years to 40 Years. Per ClinicalTrials.gov, last updated 2026-03-25.

Sponsored by Gdansk University of Physical Education and Sport · Observational

From the registry’s dates

  • Primary completion was expected by May 2026, 6 months ago, but the record still lists the study as recruiting.
  • Started Mar 2025; still recruiting 1 year 7 months later.
Study type
Observational
Model
Other
Time perspective
Other
Enrollment
30
Ages
19 Years to 40 Years
Sex
All
01

Study summary

The purpose of this study is to evaluate the effects of four-week training interventions-Nordic Hamstring Exercise, plyometric training, and neuromuscular training-combined with Super Inductive Stimulation (SIS) on hamstring muscle strength, balance, and motor performance.

Read the detailed description

This randomized controlled study evaluates the effects of three four-week training interventions-Nordic Hamstring Exercise, plyometric training, and neuromuscular training-performed alone or in combination with Super Inductive Stimulation (SIS) in physically active adults.

The study is conducted in three independent stages, each corresponding to a specific training modality. Within each stage, participants are randomly allocated to one of four parallel groups: (1) training combined with SIS, (2) training only, (3) SIS only, or (4) control (no change in habitual physical activity). This design enables assessment of both isolated and combined effects of exercise and electromagnetic stimulation.

All interventions are delivered over a four-week period under supervision. Training protocols are standardized and specific to the intervention type, targeting eccentric strength (Nordic Hamstring Exercise), explosive performance (plyometric training), or neuromuscular control (neuromuscular training).

SIS is applied to the hamstring muscle group using a high-intensity electromagnetic stimulation device, with standardized parameters across participants.

A familiarization phase is conducted prior to the intervention to ensure consistency in procedures. Adherence and protocol compliance are monitored throughout the study.

This study aims to determine the relative and combined effectiveness of these interventions in improving neuromuscular performance in physically active individuals

02

Conditions studied

  • Hamstring Injury

Keywords

  • plyometric
  • neuromuscular
03

In context

Lead sponsor

Gdansk University of Physical Education and Sport is the lead sponsor of 37 studies on the registry; 11 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
19 Years to 40 Years
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Physically active individuals aged 19-40 years, performing a minimum of two training sessions per week.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Healthy individuals aged 19-40,
  • Without injuries,
  • Physically active persons, athletes.

Exclusion criteria

Exclusion Criteria:

  • periods of peak training load specific to the athlete's discipline,
  • evidence of overload-related pathology in the knee, hip, or lumbosacral joints,
  • the presence of any pain symptoms,
  • muscle fatigue or indicators of overtraining,
  • engagement in strength-based sports within several weeks preceding competition,
  • active inflammatory conditions involving osseous, articular, or ligamentous structures of the lower limbs,
  • a history of injury or surgical intervention within the 6 months prior to the study intervention.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

05

Study design

Observational model
Other
Time perspective
Other
Enrollment
30 participants (estimated)
Patient registry
No

Groups and cohorts

  • Nordic Hamstring Exercises + SIS stimulation

    The participants will be randomly assigned to four research groups. The first research group will undergo a four-week Nordic Hamstring Exercise training program combined with Super Inductive Stimulation applied to the hamstring muscle group. The second research group will perform a four-week Nordic Hamstring Exercise training program. The third research group will undergo a four-week series of Super Inductive Stimulation sessions applied to the hamstring muscle group. The fourth group, which will serve as the control group, will not change their physical activity habits.

    Other: Nordic Hamstring Exercises + SIS stimulation

  • Plyometric traning + SIS stimulation

    The participants will be randomly assigned to four research groups. The first research group will undergo a four-week plyometric training program combined with Super Inductive Stimulation applied to the hamstring muscle group. The second research group will perform a four-week plyometric training program. The third research group will undergo a four-week series of Super Inductive Stimulation sessions applied to the hamstring muscle group. The fourth group, which will serve as the control group, will not change their physical activity habits.

    Other: Plyometric traning + SIS stimulation

  • Neuromuscular traning + SIS stimulation

    The participants will be randomly assigned to four research groups. The first research group will undergo a four-week neuromuscular training program combined with Super Inductive Stimulation applied to the hamstring muscle group. The second research group will perform a four-week neuromuscular training program. The third research group will undergo a four-week series of Super Inductive Stimulation sessions applied to the hamstring muscle group. The fourth group, which will serve as the control group, will not change their physical activity habits.

    Other: Neuromuscular traning + SIS stimulation

  • Super Inductive Stimulation (SIS) Intervention

    Super Inductive Stimulation (SIS) uses a high-intensity electromagnetic field (28 kT/s). The stimulus, induced by a coil placed in the applicator, generates depolarization of neuromuscular tissue. As a result, SIS evokes an action potential in the neuromuscular tissue, leading to the strengthening of weakened muscles. Due to the methodology of this intervention, the procedures are performed once per week over a period of 4 weeks.

    Other: Super Inductive Stimulation (SIS) Intervention

Interventions

  • OtherNordic Hamstring Exercises + SIS stimulation

    Nordic Hamstring Exercise training lasts 4 weeks, during which the participant performs 3 sets, each consisting of 3 repetitions of the NHE. After each set, a 2-minute passive rest period follows, during which the participant recovers. In the first week, the participant trains under the supervision of the instructor, while in the following three weeks the exercises are performed at home after prior instruction.

  • OtherPlyometric traning + SIS stimulation

    The intervention lasts 4 weeks, during which participants train three times per week. The program consists of single-leg and double-leg jumps, vertical jumps, lateral jumps, and forward jumps, all performed on a stable surface. A principle of progressive overload is applied, with gradual increases in training intensity, volume, and jump height. The progression begins with lower intensity exercises, single-joint movements, and less complex techniques, and advances to higher intensity exercises, multi-joint movements, and more complex techniques.

  • OtherNeuromuscular traning + SIS stimulation

    The intervention lasts 4 weeks, with participants training three times per week. The program focuses on improving dynamic stability and incorporates the use of BOSU equipment. Exercises include multitask movements performed on unstable surfaces as well as exercises with eyes closed. During the first week, exercises are performed on a stable surface to improve balance while standing on one leg with eyes open and closed. In the following weeks, exercises on unstable surfaces are introduced, emphasizing the maintenance of proper posture on either one or both legs during multitask activities. In the third week, dynamic exercises on unstable surfaces are added, such as single-leg squats. In the final week, jumps and hops are incorporated. To further increase difficulty, additional load is introduced in the form of medicine balls weighing between 2 and 8 kilograms.

  • OtherSuper Inductive Stimulation (SIS) Intervention

    uses a high-intensity electromagnetic field (28 kT/s). The stimulus, induced by a coil placed in the applicator, generates depolarization of neuromuscular tissue

06

What researchers measure

Primary outcomes

  1. Medial-Lateral Stability Index (MLSI)

    Assessment of medial-lateral postural stability using a balance platform

    Time frame: Baseline and immediately post-intervention (Week 4)

  2. Overall Stability Index (OSI)

    Assessment of overall postural stability using a balance platform

    Time frame: Baseline and immediately post-intervention (Week 4)

  3. Anteroposterior Stability Index (APSI)

    Assessment of anteroposterior postural stability using a balance platform

    Time frame: Baseline and immediately post-intervention (Week 4)

  4. Maximal hamstring muscle strength

    Maximal voluntary strength of the hamstring muscles will be assessed bilaterally using a standardized strength testing protocol

    Time frame: Baseline and immediately post-intervention (Week 4)

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Mar 2025 (actual). Primary completion is estimated for May 2026, 13 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 11, 2025
First posted
Mar 25, 2026
StartActual
Mar 15, 2025
Primary completionEst.
May 1, 2026
CompletionEst.
May 1, 2026
Last update
Mar 25, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Mar 25, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07492732
Lead sponsor
Gdansk University of Physical Education and Sport
Responsible party
Ewelina Perzanowska (Principal Investigator, Gdansk University of Physical Education and Sport) — Principal investigator
First posted
Mar 25, 2026
Start date
Mar 15, 2025
Primary completion
May 1, 2026 (estimated)
Completion
May 1, 2026 (estimated)
Last update
Mar 25, 2026

Study contacts

Ewelina Perzanowska, PhD
Contact
ewelina.perzanowska@awf.gda.pl
791597673
Ewelina Perzanowska, PhD
study chair · Department of Kinesytherapy

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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