Effects of Resistance Training With High vs. Light-moderate Loads on Muscle-tendon Function in the Elderly

Sponsor
University of Castilla-La Mancha (Other)
Overall Status
Completed
CT.gov ID
NCT03724461
Collaborator
Ministerio de Economía y Competitividad, Spain (Other), Biomedical Research Networking Center on Frailty and Healthy Aging (CIBERFES) (Other)
55
1
5
30.3
1.8

Study Details

Study Description

Brief Summary

There are no unbiased studies that have analyzed the effects of resistance training with traditional, heavy versus light-moderate loads on muscle, tendon and bone in elderly people.

The purpose of the present study is to assess the effects on muscle mass and function, tendon and bone of two different training intensities, light-moderate vs. heavy load, in people older than 65 years old.

The study will be carried out with a randomized controlled design. Participants will perform single training sessions and a 12-wk dynamic resistance training program on the knee extensors with different training intensities on each leg. One leg will train with heavy loads and the other one will train with light-moderate loads, but matching the load x repetitions performed by the contralateral side.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: High Intensity resistance training (12 weeks)
  • Behavioral: Light-moderate intensity resistance training (12 weeks)
  • Behavioral: Control (12 weeks)
  • Behavioral: One High Intensity resistance training session
  • Behavioral: One Light-moderate intensity resistance training session
N/A

Detailed Description

The decline in muscle function provoked by the aging process and frailty are directly related to decreases in mobility and the ability to perform the so called "daily life activities". Resistance training is especially useful at this stage, given that it is an effective and widely applicable intervention to control and revert sarcopenia, and the deterioration of tendon and bone function. Despite of the effectiveness of heavy load resistance training, a controversy has arisen in the last years about the effects of lower load resistance training programs to achieve similar adaptations. This is because most of the studies that have compared light-moderate versus heavy load programs did not control the differences in total training load, measured as the overall mechanical work performed during the training program. Therefore, there are no unbiased studies that have analyzed the effects of resistance training with traditional, heavy versus light-moderate loads on muscle, tendon and bone in elderly people.

The purpose of the present study is to assess the effects on muscle mass and function, tendon and bone of two different training intensities, light-moderate vs. heavy load, in people older than 65 years old.

The studies will be carried out with a crossover (acute training sessions) and randomized controlled design (longitudinal training intervention). Participants will perform single training sessions with each resistance training intensity and a 12-wk dynamic resistance training program on the knee extensors with different training intensities on each leg. One leg will train with heavy loads and the other one will train with light-moderate loads, but matching the load x repetitions performed by the contralateral side. Muscle adaptations (EMG, muscle size and architecture), tendon mechanical properties, bone mineral density, blood parameters and life quality will be analyzed before and after the cessation of the training program.

Study Design

Study Type:
Interventional
Actual Enrollment :
55 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Effects of Resistance Training With High vs. Light-moderate Loads on Muscle-tendon Function in the Elderly
Actual Study Start Date :
Sep 1, 2017
Actual Primary Completion Date :
Mar 12, 2020
Actual Study Completion Date :
Mar 12, 2020

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: High intensity vs Control (12 weeks)

8 weeks of baseline period plus an exercise program where one leg undergoes High Intensity resistance training (12 weeks) and the other leg is established as control.

Behavioral: High Intensity resistance training (12 weeks)
High intensity resistance training (80% of 1 repetition maximum), 2 d/wk (Longitudinal)
Other Names:
  • HIT
  • Behavioral: Control (12 weeks)
    No resistance training during the intervention period.
    Other Names:
  • CON
  • Active Comparator: Light intensity vs Control (12 weeks)

    8 weeks of baseline period plus an exercise program where one leg undergoes light-moderate intensity resistance training (12 weeks) and the other leg is established as control.

    Behavioral: Light-moderate intensity resistance training (12 weeks)
    Light-moderate intensity resistance training (40% of 1 repetition maximum), 2 d/wk (Longitudinal)
    Other Names:
  • LIT
  • Behavioral: Control (12 weeks)
    No resistance training during the intervention period.
    Other Names:
  • CON
  • Experimental: High vs Light intensity (12 weeks)

    8 weeks of baseline period plus an exercise program where one leg undergoes High Intensity resistance training (12 weeks) and the other leg undergoes light-moderate intensity resistance training.

    Behavioral: High Intensity resistance training (12 weeks)
    High intensity resistance training (80% of 1 repetition maximum), 2 d/wk (Longitudinal)
    Other Names:
  • HIT
  • Behavioral: Light-moderate intensity resistance training (12 weeks)
    Light-moderate intensity resistance training (40% of 1 repetition maximum), 2 d/wk (Longitudinal)
    Other Names:
  • LIT
  • Experimental: High intensity (Acute)

    Analysis of the effects of one High Intensity resistance training session, with a crossover design.

    Behavioral: One High Intensity resistance training session
    High intensity resistance training, 1 training session
    Other Names:
  • HIT (Acute)
  • Experimental: Light intensity (Acute)

    Analysis of the effects of one Light-moderate Intensity resistance training session, with a crossover design.

    Behavioral: One Light-moderate intensity resistance training session
    Light-moderate intensity resistance training, 1 training session
    Other Names:
  • LIT (Acute)
  • Outcome Measures

    Primary Outcome Measures

    1. Acute change in muscle size (cross sectional area, cm2) [Change from baseline at 5 minutes after a training session]

      Ultrasound-based determination quadriceps muscle size and architecture.

    2. Change in muscle size (cross sectional area, cm2) [Change from baseline to week 12]

      Ultrasound-based determination quadriceps muscle size and architecture.

    3. Acute change in muscle function (N) [Change from baseline at 5 minutes after a training session]

      Force-velocity profile of the single-leg press exercise

    4. Change in muscle function (N) [Change from baseline to week 12]

      Force-velocity profile of the single-leg press exercise

    Secondary Outcome Measures

    1. Change in patellar tendon stiffness (N/mm) [Change from baseline to week 12]

      Ultrasound and force-based measures of tendon mechanical properties.

    2. Acute change in patellar tendon stiffness (N/mm) [Change from baseline at 5 minutes after a training session]

      Ultrasound and force-based measures of tendon mechanical properties.

    3. Change in muscle mass (kg) [Change from baseline to week 12]

      Lean mass determined by Dual energy X-ray absorptiometry

    4. Change in bone mass (g) [Change from baseline to week 12]

      Bone mineral content determined by Dual energy X-ray absorptiometry

    5. Acute change in muscle excitation (mV) [Change from baseline at 5 minutes after a training session]

      Electromyographic activity of the knee extensor and flexor muscles during strength assessment and training

    6. Change in muscle excitation (mV) [Change from baseline to week 12]

      Electromyographic activity of the knee extensor and flexor muscles during strength assessment and training

    7. Change in physical function [Change from baseline to week 12]

      Short Physical Performance Battery

    8. Blood analysis: Acute change in oxidative stress [Change from baseline at 5 minutes after a training session]

      Carbonyl proteins (plasma concentration)

    9. Blood analysis: Change in oxidative stress [Change from baseline to week 12]

      Carbonyl proteins (plasma concentration)

    10. Blood analysis: Acute change in Inflammation [Change from baseline at 5 minutes after a training session (Acute)]

      Interleukin 6, Tumoral necrosis factor Alpha, C reactive protein (plasma concentration)

    11. Blood analysis: Change in inflammation [Change from baseline to week 12]

      Interleukin 6, Tumoral necrosis factor Alpha, C reactive protein (plasma concentration)

    12. Blood analysis: Acute change in anabolic processes [Change from baseline at 5 minutes after a training session]

      Testosterone, growth hormone, Insulin growth factor-1 (plasma concentration)

    13. Blood analysis: Change in anabolic processes [Change from baseline to week 12]

      Testosterone, growth hormone, Insulin growth factor-1 (plasma concentration)

    14. Blood analysis: Acute change in catabolic processes [Change from baseline at 5 minutes after a training session]

      Cortisol, Creatin kinase (plasma concentration)

    15. Blood analysis: Change in catabolic processes [Change from baseline to week 12]

      Cortisol, Creatin kinase (plasma concentration)

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    65 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • 65 years and older,

    • non-institutionalized

    • passed physical examination including physical function assessment (no frailty status; SPPB >7 points)

    Exclusion Criteria:
    • Neurological, musculoskeletal, or other disorder that would preclude completing resistance training and all performance tests

    • Uncontrolled hypertension, unstable or exercise-induced angina pectoris or myocardial ischemia or any other medical condition that would interfere with testing or increase one's risk of complications during exercise.

    • History of regular resistance exercise during the previous 3 years

    • Knee prosthesis

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Universidad de Castilla-La Mancha, Laboratorio de Actividad Física y Función Muscular. Campus de la Fábrica de Armas. Avda. Carlos III s/n Toledo Spain 45071

    Sponsors and Collaborators

    • University of Castilla-La Mancha
    • Ministerio de Economía y Competitividad, Spain
    • Biomedical Research Networking Center on Frailty and Healthy Aging (CIBERFES)

    Investigators

    • Principal Investigator: Luis M. Alegre, PhD, Associate Professor

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Luis M. Alegre, Associate Professor, University of Castilla-La Mancha
    ClinicalTrials.gov Identifier:
    NCT03724461
    Other Study ID Numbers:
    • DEP2015-69386-R
    First Posted:
    Oct 30, 2018
    Last Update Posted:
    Jun 16, 2020
    Last Verified:
    Jun 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Luis M. Alegre, Associate Professor, University of Castilla-La Mancha
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 16, 2020