NCT07492732

Brief 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.

Trial Health

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Mar 2025

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 15, 2025

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

September 11, 2025

Completed
7 months until next milestone

First Posted

Study publicly available on registry

March 25, 2026

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2026

Completed
Last Updated

March 25, 2026

Status Verified

March 1, 2026

Enrollment Period

1.1 years

First QC Date

September 11, 2025

Last Update Submit

March 19, 2026

Conditions

Keywords

plyometricneuromuscular

Outcome Measures

Primary Outcomes (4)

  • Medial-Lateral Stability Index (MLSI)

    Assessment of medial-lateral postural stability using a balance platform

    Baseline and immediately post-intervention (Week 4)

  • Overall Stability Index (OSI)

    Assessment of overall postural stability using a balance platform

    Baseline and immediately post-intervention (Week 4)

  • Anteroposterior Stability Index (APSI)

    Assessment of anteroposterior postural stability using a balance platform

    Baseline and immediately post-intervention (Week 4)

  • Maximal hamstring muscle strength

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

    Baseline and immediately post-intervention (Week 4)

Study Arms (4)

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

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

Super Inductive Stimulation (SIS) Intervention

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.

Nordic Hamstring Exercises + 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.

Plyometric 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.

Neuromuscular traning + SIS stimulation

Eligibility Criteria

Age19 Years - 40 Years
Sexall
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

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

You may qualify if:

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

You may not qualify if:

  • 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,
  • clinically relevant 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Gdansk University of Physical Education and Sport

Gdansk, 80-336, Poland

RECRUITING

MeSH Terms

Interventions

Methods

Intervention Hierarchy (Ancestors)

Investigative Techniques

Study Officials

  • Ewelina Perzanowska, PhD

    Department of Kinesytherapy

    STUDY CHAIR

Central Study Contacts

Ewelina Perzanowska, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

September 11, 2025

First Posted

March 25, 2026

Study Start

March 15, 2025

Primary Completion

May 1, 2026

Study Completion

May 1, 2026

Last Updated

March 25, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations