Acute Effect of Resistance Exercise, Neuromuscular Electrical Stimulation, and Transcutaneous Electrical Stimulation Applications on Muscle Activation
1 other identifier
interventional
21
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started May 2022
Shorter than P25 for not_applicable
1 active site
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
May 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2023
CompletedFirst Submitted
Initial submission to the registry
June 7, 2023
CompletedFirst Posted
Study publicly available on registry
August 30, 2023
CompletedAugust 30, 2023
August 1, 2023
5 months
June 7, 2023
August 27, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Superficial electromyography
Muscle activation measurement
through study completion, an average of 1 year
Study Arms (4)
Resistance exercise
EXPERIMENTALResistance exercise
Neuromuscular electrical stimulation
EXPERIMENTALNeuromuscular electrical stimulation
Transcutaneous electrical stimulation
EXPERIMENTALTranscutaneous electrical stimulation
Control
NO INTERVENTIONNo intervention
Interventions
Resistance exercise, Neuromuscular electrical stimulation, and Transcutaneous electrical stimulation
Eligibility Criteria
You may qualify if:
- After providing detailed information about the study, individuals who had agreed to participate in the research were included in the study.
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Gazi Universitylead
Study Sites (1)
Barış SEVEN
Izmir, Çiğli, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Ph.D. research assistant
Study Record Dates
First Submitted
June 7, 2023
First Posted
August 30, 2023
Study Start
May 1, 2022
Primary Completion
October 1, 2022
Study Completion
January 1, 2023
Last Updated
August 30, 2023
Record last verified: 2023-08
Data Sharing
- IPD Sharing
- Will not share