- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06838481
Effects of Overload Eccentric and Concentric Resistance Training on the Cost of Walking, Muscle-tendon and Jumping Performance in Healthy Older Individuals (EOECORT-COM-JP)
Study Overview
Status
Conditions
Detailed Description
Normal aging is characterized by a decline in neuromuscular and mobility functions. By the age of 70, maximal voluntary force production decreases by approximately 60%, accompanied by a ~25% reduction in muscle volume and quality, leading to sarcopenia. Alongside changes in muscle protein content, composition, and mitochondrial biochemistry, aging also affects tendon properties. While healthy aging does not significantly alter tendon size, it reduces tendon stiffness, which can delay force transmission. These changes in muscle-tendon function contribute to slower walking speeds and impaired static and dynamic balance.
One of the most significant functional changes with aging is the increased metabolic cost of walking. Older individuals require ~20% more metabolic energy to walk the same distance as younger adults, yet the underlying reasons remain unclear. While walking training has been shown to reduce metabolic costs in older adults, no studies have attempted to reduce this 20% age-related difference using alternative interventions.
Resistance training induces adaptations in muscle-tendon function by requiring participants to overcome external loads. Traditional resistance training combines concentric (muscle shortening) and eccentric (muscle lengthening) contractions, but eccentric training has received increasing attention due to its superior benefits in muscle strength and mass improvement. However, no studies have examined how resistance training, particularly with an eccentric focus, impacts functional and cognitive abilities or walking economy in older adults.
Objectives:
This study aims to:
- Investigate the effects of resistance training, particularly eccentric-focused training, on muscle-tendon function and walking economy in older adults.
- Examine whether these changes translate into improved neuromuscular and cognitive functions.
- Determine if improved tendon stiffness leads to more efficient force transmission, reducing walking energy expenditure.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Budapest
-
Budapest XII., Budapest, Hungary, 1037
- Hungarian University of Sports Science, Budapest, Hungary
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
• Healthy men and women aged 60+ (intervention study).
- No significant cognitive or cardiovascular impairments.
Exclusion Criteria:
• Acute injuries or history of severe tendon injuries (Achilles or patellar tendon rupture).
- Tendinopathy or chronic musculoskeletal disorders.
- Hypertension, unless controlled with medication.
- Neurological or psychiatric disorders (dementia, mild cognitive impairment).
- Metabolic diseases affecting muscle/tendon function,
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Concentric overload resistance training
Receive Concentric overload resistance training
|
Other Names:
|
|
Experimental: Eccentric overload resistance training
Receive Eccentric overload resistance training
|
|
|
Placebo Comparator: Active control group
walking intervention
|
Walking
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Walking metabolic cost
Time Frame: Through study completion, an average of 1.5 year
|
Assessed using spirometry at different speeds (J/kg/m)
|
Through study completion, an average of 1.5 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Maximum isometric voluntary contraction
Time Frame: Through study completion, an average of 1.5 year
|
Maximum isometric voluntary force using a dynamometer.
(Nm)
|
Through study completion, an average of 1.5 year
|
|
Patella and Achilles tendon stiffness
Time Frame: Through study completion, an average of 1.5 year
|
Stiffness is the slope of the force elongation curve using dynamometer combining with Ultrasound (N/mm)
|
Through study completion, an average of 1.5 year
|
|
Vastus lateralis and Gastrocnemius muscle thickness & tendon thickness
Time Frame: Through study completion, an average of 1.5 year
|
VL, GC, and Achilles tendon & patellar tendon will be assessed using Ultrasound images (mm)
|
Through study completion, an average of 1.5 year
|
|
Whole leg muscle mass
Time Frame: Through study completion, an average of 1.5 year
|
Whole leg muscle mass via DEXA scan.(Kg)
|
Through study completion, an average of 1.5 year
|
|
Jump efficiency
Time Frame: Through study completion, an average of 1.5 year
|
squat jump and Countermovement jump height (cm) jump efficiency (%)
|
Through study completion, an average of 1.5 year
|
|
Cognitive Assessments
Time Frame: Through study completion, an average of 1.5 year
|
Cognitive tests: Executive function, working memory, and processing speed using some questionnaires with score values. Reaction Time (milliseconds, ms) Score (points or errors) - Based on correct/incorrect responses in tasks Number of correct responses per second (responses/sec) |
Through study completion, an average of 1.5 year
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Prof. DR. Tibor Hortobágyi Hortobágyi, Hungarian University of Sports Science, Department of Kinesioogy, Budapest, Hungary
Publications and helpful links
General Publications
- Malatesta D, Canepa M, Menendez Fernandez A. The effect of treadmill and overground walking on preferred walking speed and gait kinematics in healthy, physically active older adults. Eur J Appl Physiol. 2017 Sep;117(9):1833-1843. doi: 10.1007/s00421-017-3672-3. Epub 2017 Jul 7.
- Thomas EE, De Vito G, Macaluso A. Speed training with body weight unloading improves walking energy cost and maximal speed in 75- to 85-year-old healthy women. J Appl Physiol (1985). 2007 Nov;103(5):1598-603. doi: 10.1152/japplphysiol.00399.2007. Epub 2007 Sep 6.
- Valenti G, Bonomi AG, Westerterp KR. Multicomponent Fitness Training Improves Walking Economy in Older Adults. Med Sci Sports Exerc. 2016 Jul;48(7):1365-70. doi: 10.1249/MSS.0000000000000893.
- Hunter GR, Fisher G, Neumeier WH, Carter SJ, Plaisance EP. Exercise Training and Energy Expenditure following Weight Loss. Med Sci Sports Exerc. 2015 Sep;47(9):1950-7. doi: 10.1249/MSS.0000000000000622.
- Hunter GR, McCarthy JP, Bryan DR, Zuckerman PA, Bamman MM, Byrne NM. Increased strength and decreased flexibility are related to reduced oxygen cost of walking. Eur J Appl Physiol. 2008 Nov;104(5):895-901. doi: 10.1007/s00421-008-0846-z. Epub 2008 Aug 29.
- Godges JJ, MacRae PG, Engelke KA. Effects of exercise on hip range of motion, trunk muscle performance, and gait economy. Phys Ther. 1993 Jul;73(7):468-77. doi: 10.1093/ptj/73.7.468.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- TE-KEB/No11/2024 (Other Identifier: Hungarian University of sports science)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Sharing Time Frame
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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