MedTrace Logo

The Effect of Acute Resistance Exercise on Inhibitory Control

NCT05311202 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 175

Last updated 2022-05-13

No results posted yet for this study

Summary

The current study is a five-arm, single bout program aiming to assess the effects of training volume and intensity of acute resistance exercise on inhibitory control on neurocognitive function with respect to event-related potential in adults aged 20 - 26 years.

Conditions

  • Exercise
  • Cognitive Function

Interventions

BEHAVIORAL

low-volume moderate-intensity group

The interventional program will include (1) 5 minutes of warm-up and aerobic exercise from light to moderate intensity; (2) 20 minutes of two sets of moderate intensity resistance exercise with 10 repetitions; (3) 5 minutes of cool down

BEHAVIORAL

moderate-volume moderate-intensity group

The interventional program will include (1) 5 minutes of warm-up and aerobic exercise from light to moderate intensity; (2) 30 minutes of three sets of moderate intensity resistance exercise with 10 repetitions; (3) 5 minutes of cool down

BEHAVIORAL

high-volume moderate-intensity group

The interventional program will include (1) 5 minutes of warm-up and aerobic exercise from light to moderate intensity; (2) 40 minutes of four sets of moderate intensity resistance exercise with 10 repetitions; (3) 5 minutes of cool down

BEHAVIORAL

moderate-volume low-intensity group

The interventional program will include (1) 5 minutes of warm-up and aerobic exercise from light to moderate intensity; (2) 35 minutes of four sets of low intensity resistance exercise with 20 repetitions; (3) 5 minutes of cool down

BEHAVIORAL

Control group

Reading a book related to cognitive function \& exercise for 40 minutes

Sponsors & Collaborators

  • National Taiwan Normal University

    lead OTHER

Principal Investigators

  • Yu-Kai Chang, Ph.D. · Department of Physical Education and Sport Sciences, National Taiwan Normal University

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
26 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-04-01
Primary Completion
2022-09-30
Completion
2022-12-31

Countries

  • Taiwan

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05311202 on ClinicalTrials.gov