Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2026-03-26 @ 3:16 PM
Ignite Modification Date:
2026-03-26 @ 3:16 PM
NCT ID:
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.
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
Study:
NCT07492732
Study Brief:
Protocol Section:
NCT07492732