Tendon Adaptations to Training - Effect of Ageing (TAGE)

• ClinicalTrials.gov Identifier: NCT03079180
• Recruitment Status: Unknown
• First Posted: March 14, 2017
• Last Update Posted: March 14, 2017
• Sponsor: Université de Technologie de Compiegne
• Collaborators: Centre Hospitalier Compiègne-Noyon; University of Copenhagen
• Information provided by (Responsible Party): Jean-Francois GROSSET, Université de Technologie de Compiegne

Tracking Information

• First Submitted Date: February 9, 2017
• First Posted Date: March 14, 2017
• Last Update Posted Date: March 14, 2017
• Actual Study Start Date: February 13, 2017
• Estimated Primary Completion Date: July 28, 2017 (Final data collection date for primary outcome measure)

Current Primary Outcome Measures (submitted: March 7, 2017)

• Time-course change of tendon size [ Time Frame: T-4weeks (4 weeks before starting intervention), T0 (before starting intervention), T+4weeks (after 4 weeks of intervention), T+8weeks (after 8 weeks of intervention), T+12weeks (at the end of the 12 weeks of intervention) ]
  Tendon size (tendon length and cross sectional area (CSA)) will be assessed using MRI.
• Time-course change of tendon mechanics (Elastic modulus of the tendon) [ Time Frame: T-4weeks (4 weeks before starting intervention), T0 (before starting intervention), T+4weeks (after 4 weeks of intervention), T+8weeks (after 8 weeks of intervention), T+12weeks (at the end of the 12 weeks of intervention) ]
  Tendon stiffness will be evaluated during voluntary plantar flexion contraction where force and elongation is measured using a force transducer and ultrasound, respectively. Tendon size will be assessed using MRI. Elastic modulus will be calculated based on stiffness and size of tendon.

• Original Primary Outcome Measures: Same as current
• Change History: No Changes Posted

Current Secondary Outcome Measures (submitted: March 7, 2017)

• Time-course change of plantar flexion muscle strength [ Time Frame: T-4weeks (4 weeks before starting intervention), T0 (before starting intervention), T+4weeks (after 4 weeks of intervention), T+8weeks (after 8 weeks of intervention), T+12weeks (at the end of the 12 weeks of intervention) ]
  Plantar flexion muscle strength will be assessed using a specifically designed ankle ergometer under isometric contraction.
• Time-course change of calf muscle size [ Time Frame: T-4weeks (4 weeks before starting intervention), T0 (before starting intervention), T+4weeks (after 4 weeks of intervention), T+8weeks (after 8 weeks of intervention), T+12weeks (at the end of the 12 weeks of intervention) ]
  Calf muscle size (i.e. cross sectional area and volume) will be assessed using MRI.
• Time-course change of quadriceps muscle strength [ Time Frame: T-4weeks (4 weeks before starting intervention), T0 (before starting intervention), T+4weeks (after 4 weeks of intervention), T+8weeks (after 8 weeks of intervention), T+12weeks (at the end of the 12 weeks of intervention) ]
  Quadriceps muscle strength will be assessed using a specifically designed knee ergometer under isometric contraction.
• Time-course change of quadriceps muscle size [ Time Frame: T-4weeks (4 weeks before starting intervention), T0 (before starting intervention), T+4weeks (after 4 weeks of intervention), T+8weeks (after 8 weeks of intervention), T+12weeks (at the end of the 12 weeks of intervention) ]
  Quadriceps muscle size (i.e. cross sectional area and volume) will be assessed using MRI.

• Original Secondary Outcome Measures: Same as current
• Current Other Pre-specified Outcome Measures: Not Provided
• Original Other Pre-specified Outcome Measures: Not Provided

Descriptive Information

• Brief Title: Tendon Adaptations to Training - Effect of Ageing
• Official Title: Effect of Different Strength Training Intensities on Achilles and Patellar Tendon Adaptations With Aging
• Brief Summary: Tendons are essential structures for transmitting muscle forces to skeletal structures. A stiffer tendon will transmit muscle force faster, and then allow faster movement. Moreover, tendons are a living tissue and respond to mechanical forces by changing their metabolism as well as their structural and mechanical properties. The aim of the present study is to answer essential questions remaining unanswered that are necessary in order to optimize physical activity with ageing in humans, and thus improve quality of life in elderly. The main questions are: What is the minimal training intensity leading to tendon adaptations? What is the time-course of tendon adaptations? Does the same loading protocol lead to similar tendon adaptations for different tendons (Achilles vs Patellar) and does the same training program lead to identical tendon adaptations with age (25yrs vs 75yrs)? To answer these questions, tendon architecture and mechanical properties will be investigated in humans of different age and applying different training intensities. The kinematic of the tendon adaptations due to these different training characteristics will also be investigated. The training protocol will be applied on plantar flexors and knee extensors. MRI and ultrasound techniques as well as the use of ankle and knee ergometers will allow the quantification of possible modifications in tendon architecture and mechanical properties (tendon stiffness and Young's Modulus). This will be assessed in vivo, using ultrasound images to assess tendon displacement during an incremental maximal contraction.

Detailed Description

Given the aging population demographics, and the barriers that exist in this population in terms of exercise participation, determining the level of exercise intensity required and the time-course to induce tendon adaptations is of paramount importance in this population. Therefore the purpose of this study is to:

1. determine whether a low intensity exercise training program (resistance 55% 1RM) affects tendon architecture and mechanical properties with aging,
2. compare these effects to those of a higher intensity exercise training protocol (resistance 80% 1RM) with a match training work with regards to the low intensity exercise training group,
3. evaluate the time course of tendon adaptations (architecture and mechanical properties) for the two training conditions with aging,
4. compare the effect of an identical training protocol applied on two different muscle groups (triceps surae vs quadriceps muscles) on Patellar and Achilles tendon adaptations.

Every subject recruited (Two groups composed of males aged between 65 and 85 years, and one group of young subjects (between 18 and 30 years)) will be asked to take part in a training program applied on the calf and quadriceps muscle groups on both legs. All subjects will be assessed 4 weeks before starting the intervention program (T-4w), at time zero (T0) and every four weeks during 12 weeks (T4w, and T8w). The investigation 4 weeks before starting the training program will allow using each subject as its own control. The intervention will involve a maximum of forty five (45) minutes training sessions 3 times per week. Subjects will be subjected to the same battery of baseline assessments (T-4w, and T0), during the training procedure (T4w, and T8w), and following the 12-weeks intervention period (T12w).

The effect of aging and different loading interventions on Achilles and Patellar tendon will be investigated for the following parameters:

• Tendon mechanical properties (stiffness and Young's Modulus) using US technique to assess Achilles and Patellar tendon displacement during an incremental maximal contraction.
• Tendon architecture using MRI technique to assess Achilles and Patellar tendon cross-sectional area, tendon length and moment arm.
• Maximal voluntary contraction (MVC)
• Muscle architecture using MRI technique.

Thus all these data will allow defining an optimal training intensity for physical activity of elderly persons.

• Study Type: Interventional
• Study Phase: Not Applicable
• Study Design: Allocation: Randomized; Intervention Model: Parallel Assignment; Masking: Single (Outcomes Assessor); Primary Purpose: Supportive Care

Condition

• Aging
• Exercise Training
• Connective Tissue
• Skeletal Muscle

Intervention

• Other: Strength training at 80% 1RM
  Detailed in Arms section's
• Other: Strength training at 55% 1RM
  Detailed in Arms section's

Study Arms

• Experimental: Aged & strength training at 80% 1RM

  Subjects: 20 subjects aged between 65 and 85 years

  Training programs:

  Frequency: 3 training sessions per week. Duration: 12 weeks. Intensity: 80% of one repetition maximum (1RM). The 1RM of the participants in each of the 3 exercises performed in the training program will be reviewed every 2 weeks during training. If 1RM increase, the training load will be adjusted accordingly.

  Training exercises: A Warm-up will first be performed on a cycle ergometer during 10min. The training intervention will then consist in performing two sets on each one of the two exercises used for Patellar tendon stress: leg extension and leg press. To stress Achilles tendon, the subjects will perform four (4) sets using a calf raise machine. The subjects will perform 4 to 8 repetitions at 80% 1RM.

  All training sessions will take place under appropriate supervision in UTC for the duration of the interventions according to the study design.

  Intervention: Other: Strength training at 80% 1RM
• Experimental: Aged & strength training at 55% 1RM

  Subjects: 20 subjects aged between 65 and 85 years

  The training program and training exercises in this group are the same as for the Aged & strength training at 80% 1RM arm except for the two following parameters.

  Training intensity: Intensity of exercises will be 55% of one repetition maximum (1RM).

  The subjects will perform 6 to 12 repetitions at 55% 1RM.

  The two training programs (55% or 80% of 1RM) are designed to be equal in volume (resistance x repetitions x sets).

  Intervention: Other: Strength training at 55% 1RM
• Experimental: Young & strength training at 55% 1RM

  Subjects: 20 subjects aged between 18 and 30 years

  The training program and training exercises in this group are the same as for the Aged & strength training at 55% 1RM arm

  Intervention: Other: Strength training at 55% 1RM

• Publications *: Létocart AJ, Mabesoone F, Charleux F, Couppé C, Svensson RB, Marin F, Magnusson SP, Grosset JF. Muscles adaptation to aging and training: architectural changes - a randomised trial. BMC Geriatr. 2021 Jan 13;21(1):48. doi: 10.1186/s12877-020-02000-0.

Recruitment Information

• Recruitment Status: Unknown status
• Estimated Enrollment (submitted: March 7, 2017): 60
• Original Estimated Enrollment: Same as current
• Estimated Study Completion Date: July 28, 2017
• Estimated Primary Completion Date: July 28, 2017 (Final data collection date for primary outcome measure)

Eligibility Criteria

Inclusion Criteria:

• Males
• Age between 18 and 30 years for the young group and between 65 and 85 years for aged group
• Physical and mental health, as assessed by clinical investigation
• Written informed consent
• Willingness to co-operate
• Non-smoker
• Not addicted to alcohol or drugs
• Habitual sedentary/low physical activity levels

Exclusion Criteria:

• BMI <20 or >28
• Height <155cm, >195cm
• Chronic disease with regular clinical treatment
• Regular drug intake
• Any metabolic or hormonal disorder
• Psychiatric conditions
• Any blood clotting disorder
• Any muscle or bone disease
• Metal implants
• Any inflammatory disease
• Metabolic or hormonal disorder
• Participation in sports at competitive rather than at a recreational level
• Fractures during the past 6 months
• Epilepsy
• Back pain
• Lower extremity trauma during the past 6 months, or currently experiencing related symptoms, or receiving treatment
• Any other condition or history that the investigator considers might increase the risk to the individual or interfere with the evaluation of data

Sex/Gender

• Sexes Eligible for Study: Male

• Ages: 18 Years to 85 Years (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Contacts: Contact information is only displayed when the study is recruiting subjects
• Listed Location Countries: France

Administrative Information

• NCT Number: NCT03079180
• Other Study ID Numbers: 2016-A00534-47
• Has Data Monitoring Committee: No

U.S. FDA-regulated Product

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No

IPD Sharing Statement

• Plan to Share IPD: No

• Responsible Party: Jean-Francois GROSSET, Université de Technologie de Compiegne
• Study Sponsor: Université de Technologie de Compiegne

Collaborators

• Centre Hospitalier Compiègne-Noyon
• University of Copenhagen

Investigators

• Principal Investigator: Franck Mabesoone, MD; Centre Hospitalier Compiegne-Noyon

• PRS Account: Université de Technologie de Compiegne
• Verification Date: March 2017