Mental Effort During Low Load Resistance Training in Older Adults
The Effect of Maximal Mental Effort During Resistance Training on Physical Function and Motor Unit Behavior in Older Adults
1 other identifier
interventional
75
1 country
1
Brief Summary
The goal of this clinical trial is to determine the effect of maximal mental effort combined with low-intensity resistance training on strength and neuromuscular function in older adults. The main questions it aims to answer are:
- Does low-intensity resistance training in combination with maximal mental effort increase strength more than low intensity resistance training alone?
- Does low-intensity resistance training in combination with maximal mental effort improve neuromuscular function more than low intensity resistance training alone? Participants will be randomly assigned to 1 of 3 groups:
- Low intensity resistance training
- Low intensity resistance training with maximal mental effort
- Control Researchers will compare groups to determine differences in changes in strength, neuromuscular function, and body composition.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jun 2026
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
June 6, 2026
CompletedFirst Submitted
Initial submission to the registry
June 30, 2026
CompletedFirst Posted
Study publicly available on registry
July 7, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2027
July 8, 2026
July 1, 2026
1.5 years
June 30, 2026
July 6, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in isokinetic strength of the knee extensors at 60 degrees per second
Dynamic strength of the knee extensors contracting at a constant velocity
Baseline, Week 8
Secondary Outcomes (16)
Change in isokinetic knee extensor muscle activation as measured by electromyography amplitude
Baseline, Week 8
Change in isometric knee extensor strength as measured by newton-meters of torque
Baseline, Week 8
Change in knee extensor muscle activation as measured by electromyography amplitude
Baseline, Week 8
Change in motor unit firing rate as measured relative to the motor unit recruitment threshold
Baseline, Week 8
Change in motor unit action potential size as measured relative to the motor unit recruitment threshold
Baseline, Week 8
- +11 more secondary outcomes
Study Arms (3)
Low Intensity Resistance Training
EXPERIMENTALThis group will perform low intensity, whole-body resistance training.
Low Intensity Resistance Training with Maximal Mental Effort
EXPERIMENTALThis group will perform low intensity, whole-body resistance training with maximal mental effort during muscle contraction.
Control
NO INTERVENTIONThis group will not perform any training and maintain their regular level of physical activity.
Interventions
This training intervention will be 8 weeks of low intensity resistance training, including whole-body and isolated muscle exercises, where participants will perform maximal mental effort by imagining maximal muscle contraction during each exercise.
This training intervention will be 8 weeks of low intensity resistance training, including whole-body and isolated muscle exercises.
Eligibility Criteria
You may qualify if:
- Body mass index between 18.5 - 33 kg·m2
- No structured physical activity in past 2 years
- Any unstable condition contradicting exercise
- Independently walk with or without assistive device
- No significant cognitive impairment
You may not qualify if:
- Score of 22 or lower on Montreal Cognitive Assessment
- Missing more than 3 training sessions (training groups only)
- Pacemaker
- Unstable angina
- Symptomatic heart failure
- Uncontrolled arrythmias
- Uncontrolled hypertension (greater or equal to 160/90)
- Myocardial infarction in the past 6 months
- Uncontrolled type 2 diabetes
- Type 1 diabetes
- Severe or unstable pulmonary conditions,
- Currently on supplemental oxygen therapy
- Severe hearing loss or visual impairment
- Alzheimer's Disease or significant cognitive impairment
- Stroke in the past 6 months or ongoing stroke-induced motor impairment
- +6 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Kennesaw State University
Kennesaw, Georgia, 30144, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Masking Details
- The mental effort aspect of the study will be concealed from subjects, so they will not be aware of any difference between training groups.
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor of Exercise Science
Study Record Dates
First Submitted
June 30, 2026
First Posted
July 7, 2026
Study Start
June 6, 2026
Primary Completion (Estimated)
December 1, 2027
Study Completion (Estimated)
December 1, 2027
Last Updated
July 8, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will not share