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Comparison of Effect of Dual-Site Transcranial Direct Current and Pulsed Current Stimulation on submaximal Isotonic contractions

Comparison of the Effects of Dual-Site Transcranial Direct Current and Pulsed Current Stimulation on Muscular Performance and Neurophysiological Responses in Submaximal Isotonic Contractions

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240424061556N1
Enrollment
15
Registered
2024-05-04
Start date
2024-05-14
Completion date
Unknown
Last updated
2024-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

The participants are healthy people..

Interventions

Intervention 1: Intervention group: In this study, all subjects will be exposed to two intervention conditions with a minimum interval of 72 hours, including 1) two-zone direct current electrical stim

Sponsors

Razi university of Kermanshah
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: Age range 18 to 30 years Women with more than 6 months of regular resistance training Body mass index (BMI) 18.5 to 24.9 kg/squared height in meters Has natural color vision Being right-handed (the dominant hand should be the right hand)

Exclusion criteria

Exclusion criteria: Having any cardiovascular, pulmonary and metabolic disease History of seizures, epilepsy or other types of neurological diseases The presence of implantable devices or pacemakers in the body Smoking and alcohol consumption

Design outcomes

Primary

MeasureTime frame
Muscle performance. Timepoint: After each set of resistance training with 50% 1RM in three sets. Method of measurement: Number of repetitions in each set × The weight has shifted.;Rating of Perceived Exertion. Timepoint: At the end of each set. Method of measurement: Using a scale of 0 to 100 borg.

Secondary

MeasureTime frame
Inhibitory control. Timepoint: Before and after the residual resistance protocol. Method of measurement: Modified Stroop test software.;Choice reaction time. Timepoint: Before and after the residual resistance protocol. Method of measurement: Selective reaction timer test software.;Pleasure scale. Timepoint: At the end of each set. Method of measurement: Using a 11-item emotion scale.;Pleasure Arousal scale. Timepoint: At the end of each set. Method of measurement: Using a 6-item pleasure Arousal scale.;Pain scale. Timepoint: At the end of each set. Method of measurement: Using a 10-item pain scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactEhsan Amiri

Razi University of Kermanshah

e.amiri@razi.ac.ir+98 83 3427 4585

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026