Acute Effect of Resistance Exercise, Neuromuscular Electrical Stimulation, and Transcutaneous Electrical Stimulation Applications on Muscle Activation

NCT ID: NCT06016660

Last Updated: 2023-08-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

21 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-05-01

Study Completion Date

2023-01-01

Brief Summary

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The aim of our study is to investigate the effects of single-session resistance exercise, neuromuscular electrical stimulation, and transcutaneous electrical stimulation on the level of muscle activation and their superiority over each other on both the ipsilateral and contralateral sides. Our randomized controlled crossover study included 21 participants (13 female, 8 male, age; 27.7±4). Transcutaneous electrical stimulation was used for sensory input. A single-session application was performed only to the right extremities of all participants, and the acute effects on muscle activation on both the ipsilateral and contralateral sides were evaluated. Muscle activation was evaluated with superficial EMG. SPSS® Statistics V22.0 software was used for statistical analysis. As a result of the statistical analysis, a significant increase in activation was found only in the sensory input application group on the ipsilateral side flexor carpi radialis (FCR) (p=0.001), flexor carpi ulnaris (FCU) (p\<0.001), flexor digitorum superficialis (FDS) (p=0.023) and flexor digitorum profundus (FDP) (p=0.003) muscles. On the contralateral side, there was an increase in activation in all muscles (FCR; p\<0.001, FCU; p=0.033, FDS; p=0.017 and FDP; p=0.001) in the resistant exercise group. In addition, there was a significant increase in the activation of certain muscles on the contralateral side in the NMES application group (FCR (p=0.049) and FDP (p=0.016) muscles) and the sensory input application group (FDP (p=0.004) and FDS (p=0.043) muscles). In situations where movement is contraindicated, ipsilateral sensory input can increase the level of muscle activation through both cortical and peripheral neural mechanisms.In addition, resistance exercise to be performed on the contralateral side can be an effective application to increase muscle activation on the ipsilateral side.

Detailed Description

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Conditions

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Motor Activity

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Resistance exercise

Resistance exercise

Group Type EXPERIMENTAL

Physiotherapy

Intervention Type OTHER

Resistance exercise, Neuromuscular electrical stimulation, and Transcutaneous electrical stimulation

Neuromuscular electrical stimulation

Neuromuscular electrical stimulation

Group Type EXPERIMENTAL

Physiotherapy

Intervention Type OTHER

Resistance exercise, Neuromuscular electrical stimulation, and Transcutaneous electrical stimulation

Transcutaneous electrical stimulation

Transcutaneous electrical stimulation

Group Type EXPERIMENTAL

Physiotherapy

Intervention Type OTHER

Resistance exercise, Neuromuscular electrical stimulation, and Transcutaneous electrical stimulation

Control

No intervention

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Physiotherapy

Resistance exercise, Neuromuscular electrical stimulation, and Transcutaneous electrical stimulation

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

• After providing detailed information about the study, individuals who had agreed to participate in the research were included in the study.

Exclusion Criteria

* Individuals with any central or peripheral nervous system disease/injury affecting the upper extremity,
* Individuals with a history of orthopedic injury that could impact the study,
* Individuals with a history of neuromuscular disease, congenital anomalies, skin infections, or cognitive impairments,
* Individuals with a history of systemic or metabolic diseases that could potentially affect the study,
* Individuals with a body mass index (BMI) above 30 kg/m2.
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Gazi University

OTHER

Sponsor Role lead

Responsible Party

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Barış SEVEN

Ph.D. research assistant

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Barış SEVEN

Izmir, Çiğli, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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EMGHealthy

Identifier Type: -

Identifier Source: org_study_id

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