CClinicalTrials.gg
RecruitingNCT06099678Updated Dec 11, 2023

Enhancing Strength Gains With the Power of the Mind

An interventional study of Elastic Band Training and Elastic Band Training with Maximal Mental Effort in Healthy, sponsored by Kennesaw State University. Recruiting at 2 sites in United States. Open to female participants aged 65 Years to 79 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-12-11.

Sponsored by Kennesaw State University · Not applicable, Interventional, and Other

From the registry’s dates

  • Primary completion was expected by Nov 2024, 1 year 11 months ago, but the record still lists the study as recruiting.
  • Started Nov 2023; still recruiting 2 years 11 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
45
Allocation
Randomized
Ages
65 Years to 79 Years
Sex
Female
01

Study summary

The goal of this clinical trial is to determine the effect of maximal mental effort combined with elastic band training on strength and neuromuscular function in healthy, older females. The main questions it aims to answer are:

  • Does elastic band training in combination with maximal mental effort increase strength more than elastic band training alone?
  • Does elastic band training in combination with maximal mental effort improve neuromuscular function more than elastic band training alone?

Participants will be randomly assigned to 1 of 3 groups:

  • Elastic band training
  • Elastic band training with maximal mental effort
  • Control

Researchers will compare groups to determine differences in changes in strength, neuromuscular function, and body composition.

Read the detailed description

Participants in both training groups will perform 6 weeks of moderate intensity, whole-body elastic band training. Participants in the control group will participate in all testing procedures but not perform any training. Participants from both groups will be instructed to maintain their normal physical activity levels and dietary habits.

All training sessions will be home-based and virtually supervised by research personnel. Participants will complete 2 training sessions in the first week and 3 training sessions per week for the remaining 5 weeks. Each training session will last about 45-60 minutes and consist of 7 exercises performed in the same order by each participant, including both multi-joint (chair squat, chest press, leg press, back row) and single-joint (knee extension, knee flexion, elbow flexion) exercises. Participants will perform 12 repetitions for each exercise for the first 3 weeks, then volume will be increased by progressing to 4 sets for the remaining 3 weeks. There will be a 60-second rest interval between sets and a similar tempo will be used between groups.

Both training groups will perform the same training protocol, but participants in the maximal mental effort group will mentally urge their muscles to contract maximally during each repetition. That is, despite using a moderate intensity, participants will imagine the feeling of maximal muscle contraction of the primary muscles during each repetition.

Several measures of strength, neuromuscular function, physical function, and body composition will be measured before and after the training or control period.

02

Conditions studied

  • Healthy
03

In context

Lead sponsor

Kennesaw State University is the lead sponsor of 9 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
65 Years to 79 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  • Between 65-79 years of age
  • Female
  • Have not engaged in structured exercise for 3 years
  • Are not reliant upon a walking aid
  • Be able to rise from a chair unassisted
  • BMI between 25-33 kg/m²
  • Have access to the internet and access to a smartphone or computer with a camera at home

Exclusion criteria

Exclusion Criteria:

  • Any history of cardiovascular, cerebrovascular, or metabolic diseases
  • Musculoskeletal injury within the past 6 months
  • Any condition affecting muscle function
  • Uncontrolled hypertension
  • Score less than 23 on the Mini-mental State Exam
  • Upon starting study, missing more than 2 training session
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
45 participants (estimated)

Study arms

  • Experimental
    Elastic Band Training

    This group will perform moderate intensity, whole-body elastic band training.

    Behavioral: Elastic Band Training

  • Experimental
    Elastic Band Training with Maximal Mental Effort

    This group will perform moderate intensity, whole-body elastic band training with maximal mental effort during muscle contraction.

    Behavioral: Elastic Band Training with Maximal Mental Effort

  • No intervention
    Control

    This group will not perform any training and maintain their regular level of physical activity.

Interventions

  • BehavioralElastic Band Training

    This training intervention will be 6 weeks of moderate-intensity elastic band training, including whole-body and isolated muscle exercises.

  • BehavioralElastic Band Training with Maximal Mental Effort

    This training intervention will be 6 weeks of moderate-intensity elastic band training, including whole-body and isolated muscle exercises, where participants will perform maximal mental effort by imagining maximal muscle contraction during each exercise.

06

What researchers measure

Primary outcomes

  1. Change in bicep curl strength as measured by load lifted in pounds

    Maximum dumbbell load lifted successfully throughout the range of motion of a bicep curl

    Time frame: Baseline, Week 7

Secondary outcomes

  1. Change in voluntary activation as measured by ratio of superimposed torque to resting twitch torque

    Voluntary activation is an estimate of neural drive and is the amplitude of superimposed torque elicited by percutaneous muscle stimulation relative to the resting twitch torque amplitude

    Time frame: Baseline, Week 7

  2. Change in handgrip strength as measured in kilograms of force

    Upper-body strength as measured by a handgrip dynamometer

    Time frame: Baseline, Week 7

  3. Change in agonist muscle activation as measured by electromyography amplitude

    A measure of the capacity at which the muscle is activitated by the nervous system

    Time frame: Baseline, Week 7

  4. Change from baseline in isokinetic muscle activation at 6 weeks

    Electromyography root mean square during isokinetic contraction divided by root mean square during isometric contraction

    Time frame: Baseline, Week 7

  5. Change in antagonist co-activation as measured by electromyography amplitude

    A measure of the capacity at which the antagonist muscle is activated by the nervous system

    Time frame: Baseline, Week 7

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

    Isometric strength of a muscle

    Time frame: Baseline, Week 7

  7. Change in isokinetic bicep strength as measured by newton-meters of torque

    Dynamic strength of a muscle contracting at a constant velocity

    Time frame: Baseline, Week 7

  8. 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

    Time frame: Baseline, Week 7

  9. Change in walking speed as measured by time taken to walk 6 meters

    Measure of lower-body physical function

    Time frame: Baseline, Week 7

  10. Change in chair rise performance as measured by number of chair rises performed in 30 seconds

    Measure of lower-body physical function

    Time frame: Baseline, Week 7

  11. Change in chair rise power by watts by a linear transducer attached to hip during chair rise test

    Product of load and velocity as determined on a linear transducer

    Time frame: Baseline, Week 7

  12. Change in muscle composition as measured by ultrasound-derived grey-scale analysis

    Echo-intensity value derived from grey-scale analysis is indicative of amount of non-contractile tissue in muscle

    Time frame: Baseline, Week 7

  13. Change in skeletal muscle size as measured by ultrasound-derived cross-sectional

    Size of a muscle

    Time frame: Baseline, Week 7

  14. Change in fat mass as measured by kilograms

    Amount of fat tissue a person possesses estimated by bioelectrical impedance analysis

    Time frame: Baseline, Week 7

  15. Change in fat-free mass as measured by kilograms

    Amount of non-fat tissue a person possesses estimated by bioelectrical impedance analysis

    Time frame: Baseline, Week 7

  16. Change in body fat percentage as measured by fat tissue relative to fat-free tissue

    Relative amount of body fat a person possesses estimated by bioelectrical impedance analysis

    Time frame: Baseline, Week 7

  17. Change in hemoglobin A1c level as measured by blood drop analysis

    Blood drop analysis, obtained from fingerstick, measure of amount of blood sugar bound to hemoglobin

    Time frame: Baseline, Week 7

  18. Change in resting heart rate as measured by beats/min using oscillatory cuff

    Measure of cardiovascular fitness

    Time frame: Baseline, Week 7

  19. Change in resting blood pressure in millimeters of mercury using oscillatory cuff

    Measure of cardiovascular fitness

    Time frame: Baseline, Week 7

  20. Change in general feeling about knee extension and bicep curl exercise

    From a -5 to +5 on the Affective Feeling Scale

    Time frame: Each exercise session of the 6-week intervention

  21. Change in grip width on elastic band as measured by distance of hand placements on band

    Indication of progression in training intensity

    Time frame: Baseline, 3 weeks, 5 weeks

Other outcomes

  1. Change in exercising heart rate

    A descriptor of the exercise physiological intensity for both training protocols

    Time frame: Each exercise session of the 6-week intervention

  2. Change in calorie consumption as measured by kilocalories determined by dietary recall

    Amount of calories consumed

    Time frame: Baseline, Week 7

  3. Change in protein consumption as measured by kilocalories determined by dietary recall

    Amount of protein consumed

    Time frame: Baseline, Week 7

  4. Change in physical activity as measured by daily step count via Garmin Venu SQ smartwatch

    Measure of physical activity level

    Time frame: Baseline, Week 7

07

Study locations

2 of 2 sites recruiting
  • Kennesaw State University
    Kennesaw, Georgia 30144, United States
    • Garrett Hester, Ph.D. · Contact
    Recruiting
  • Kennesaw State University
    Kennesaw, Georgia 30144, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 11, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06099678
Lead sponsor
Kennesaw State University
Responsible party
Garrett Hester (Associate Professor of Exercise Science, Kennesaw State University) — Principal investigator
First posted
Oct 25, 2023
Start date
Nov 1, 2023
Primary completion
Nov 2024 (estimated)
Completion
Nov 1, 2024 (estimated)
Last update
Dec 11, 2023

Study contacts

Garrett Hester, Ph.D.
Contact
ghester4@kennesaw.edu
470-578-4267
Garrett Hester, Ph.D.
principal investigator · Kennesaw State University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion