NCT06627491

Brief Summary

The goal of this randomized clinical trial is to learn if imagining fast or slow muscle contractions causes different responses for nervous system excitability and muscle function in young, healthy males and females in. The main questions are: Does imagining fast muscle contractions cause greater nervous system excitability compared to imagining slow muscle contractions? Does imagining fast muscle contractions increase muscle function compared to imagining slow muscle contractions? A control condition (rest) will be compared with two intervention conditions: imagining fast and imagining slow conditions, to determine if the fast and slow increase outcomes more than control and if fast has the greatest response. Participants will:

  • Attend 4 laboratory visits
  • Perform 50 imagined contractions fast or slow, but with no physical movement
  • Physical muscle contractions and non-invasive brain stimulation would be completed before and after each condition.

Trial Health

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Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
18

participants targeted

Target at below P25 for not_applicable healthy

Timeline
Completed

Started Oct 2024

Geographic Reach
1 country

1 active site

Status
recruiting

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

October 1, 2024

Completed
1 day until next milestone

First Submitted

Initial submission to the registry

October 2, 2024

Completed
2 days until next milestone

First Posted

Study publicly available on registry

October 4, 2024

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2025

Completed
Last Updated

October 9, 2024

Status Verified

October 1, 2024

Enrollment Period

7 months

First QC Date

October 2, 2024

Last Update Submit

October 7, 2024

Conditions

Keywords

Muscle strengthNervous SystemMotor Imagery

Outcome Measures

Primary Outcomes (2)

  • Change in rate of torque development as measured by newton-meters per second

    A measure of the capacity to increase muscle torque rapidly as determined by the slope of the torque-time curve

    Baseline, minute 20

  • Change in nervous system excitability as measured by electromyographic waveform aplitude following motor cortex stimulation

    A measure of excitability for the corticospinal tract

    Baseline, minute 20

Secondary Outcomes (5)

  • Change in isometric bicep strength as measured by newton-meters of torque

    Baseline, minute 20

  • Change in agonist muscle activation as measured by electromyography amplitude

    Baseline, minute 20

  • Change in antagonist co-activation as measured by electromyography amplitude

    Baseline, minute 20

  • Change in rate of agonist muscle activation as measured by electromyography amplitude

    Baseline, minute 20

  • Change in nervous system inhibition as measured by electromyographic waveform aplitude following motor cortex stimulation

    Baseline, minute 20

Other Outcomes (2)

  • Self-reported ability to imagine movements as measured by Movement Imagery Questionnaire-Revised as measured on a scale from 8 to 56

    Baseline

  • Level of vividness for imagining the imagined contractions as measured by 7-point likert scale as measured from 1 to 7

    20 minutes after baseline

Study Arms (3)

Control

NO INTERVENTION

Participants will rest quietly with eyes closed during the control condition.

Fast

EXPERIMENTAL

Participants will imagine 2 blocks of 25 fast muscle contractions separated by 30 sec

Behavioral: Imagined muscle contractions

Slow

EXPERIMENTAL

Participants will imagine 2 blocks of 25 slow muscle contractions separated by 30 sec

Behavioral: Imagined muscle contractions

Interventions

The intervention involved imagining, with no physical movement, of muscle contractions.

FastSlow

Eligibility Criteria

Age18 Years - 30 Years
Sexall(Gender-based eligibility)
Gender Eligibility Detailsmale and female
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Be between the ages of 18 - 30
  • Healthy (no medical conditions)
  • If female, must be taking the same monophasic oral contraceptive for the past 6 months
  • Have a body mass index between 18.5 - 30 kg/m2
  • Have not performed structured cardiovascular or resistance exercise in past 3 years
  • Be right-handed
  • Not currently taking stimulants, antipsychotic, anxiety, or depression medications
  • Have not suffered an upper extremity musculoskeletal injury within the past year

You may not qualify if:

  • If transcranial magnetic stimulation (TMS) is not deemed appropriate depending on your responses to the TMS-specific questionnaire
  • Being ambidextrous
  • Although rare, you will be excluded if discernable muscle activation responses are not possible via TMS

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kennesaw State University

Kennesaw, Georgia, 30144, United States

RECRUITING

MeSH Terms

Conditions

Neurologic Manifestations

Condition Hierarchy (Ancestors)

Nervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Central Study Contacts

Garrett Hester, Ph.D.

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor of Exercise Science

Study Record Dates

First Submitted

October 2, 2024

First Posted

October 4, 2024

Study Start

October 1, 2024

Primary Completion

May 1, 2025

Study Completion

May 1, 2025

Last Updated

October 9, 2024

Record last verified: 2024-10

Data Sharing

IPD Sharing
Will share

Non-identifying IPD will be provided upon a reasonable request.

Time Frame
Beginning 3 months and ending 5 years after the publication of results

Locations