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Clinical Trials/NCT05585502
NCT05585502CompletedNot Applicable

Impact of Muscle and Tendon Dysfunction on the Mechanics of Muscle Contraction and Locomotion Capacity in People With Type 2 Diabetes Mellitus, and Efficacy of a Passive Stretching Training Program to Counteract These Alterations

Universita di Verona2 sites in 1 country46 target enrollmentStarted: December 10, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
46
Locations
2
Primary Endpoint
Muscle and tendon stiffness differences between T2D patients and controls

Study Overview

Brief Summary

Diabetes is a chronic-degenerative metabolic disorder that has reached pandemic proportions mainly because of the increasing incidence and prevalence of type 2 diabetes mellitus (T2D).

Diabetes hurts cardiovascular function due to chronic hyperinsulinemia and hyperglycemia, along with increased advanced glycation end products (AGEs) causing nonenzymatic glycation of soft tissues, including muscle and tendon, and leading to an increase in muscle and tendon stiffness. In turn, the stiffening of the muscle-tendon complex reduces its capability to change in shape, affecting its potential for modulating the mechanical request during contraction (and locomotion), also increasing the metabolic demands during walking.

The present, multi-disciplinary, project combines several experimental methods and procedures to investigate the impact of muscle and tendon alterations on the mechanics of muscle contraction and locomotion capacity in T2D patients. In this project, we also propose a new training approach (minute oscillation stretching) to counteract these possible alterations (e.g. to decrease muscle and tendon stiffness).

Detailed Description

Diabetes is a chronic-degenerative metabolic disorder that has reached pandemic proportions, mainly because of the increasing incidence and prevalence of type 2 diabetes mellitus (T2D). According to the International Diabetes Federation (IDF, 2017), 425 million people suffer from diabetes worldwide and these may rise to 629 million in 2045 . Within this epidemiological perspective, diabetes emerges as one of the main metabolic disorders with substantial costs for regional and national sanitary systems.

Diabetes hurts cardiovascular function due to chronic hyperinsulinemia and hyperglycemia, along with increased advanced glycation end products (AGEs), pro-inflammatory cytokines, oxidative stress, obesity, dyslipidemia, and physical inactivity, all of which contribute to vascular dysfunction. In particular, several studies have shown that AGEs exert their negative effects through binding to a specific cellular receptor (RAGE), found in several cell systems such as monocytes and endothelial cells. However, little attention has been paid, so far, to alterations in the musculoskeletal system, which may contribute to the decline of the general state of health of diabetic people and may limit the therapeutic use of exercise in these subjects.

Diabetes causes non-enzymatic glycation of soft tissues, including muscle and tendon, leading to an increase in muscle and tendon stiffness. It was observed that Achilles tendon stiffness and skin connective tissue cross-linking are greater in diabetic patients compared to controls and it has been suggested that the elevated tendon stiffness may influence gait parameters. Indeed, during walking, diabetic patients display less Achilles tendon elongation, higher tendon stiffness and higher tendon hysteresis compared to healthy controls. The higher energy cost of walking in diabetic patients could thus be related to an impairment of the Achilles tendon function. The stiffening of the muscle, on the other hand, reduces its capability to change in shape, affecting its potential for modulating the mechanical request during contraction (and locomotion), also increasing the metabolic demands. Therefore, investigating the mechanical alterations caused by an increase in muscle and tendon stiffness could provide new insights into diabetes pathophysiology.

Training strategies able to reduce muscle and tendon stiffness are expected to improve muscle-tendon function and locomotor capability of diabetic patients. Even if strength and endurance training protocols allow to improve both blood glucose and muscle contractile function, they seem ineffective in reducing muscle and tendon stiffness in T2D patients. Notably, these training modalities present a significant dropout in the diabetic population, generally higher than 25%.

Static and dynamic stretching are effective in decreasing muscle and tendon stiffness but, in both cases, the decrease in stiffness is associated with a temporary decrease in muscle and tendon mechanical function.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
50 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • body mass index between 23 and 30 kg/m2
  • moderate level of physical activity in the everyday life (assessed by means of the International Physical Activity Questionnaires, IPAQ)

Exclusion Criteria

  • neuropathy of nondiabetic origin
  • severe neuropathy
  • foot ulcers
  • arterial insufficiency
  • arthritis of the ankle/foot
  • previous foot/knee surgery
  • previous Achille tendon rupture
  • previous Charcot foot
  • cardiovascular and respiratory deficits that would impede the performance of the locomotion test
  • insulin therapy

Arms & Interventions

Training group

Experimental

T2D patients and controls in the experimental group will undergo 50 telemedicine MOS sessions (15 minutes/day, 5 days/week, 10 weeks). Before the training period all subjects will participate to three different experimental sessions: during the first session a blood sample will be withdrawn and a skin biopsy will be taken; during the second session, muscle-tendon stiffness and muscle function will be evaluated; during the third session, the energy cost of walking will be determined at different speeds. After the training period and 5 weeks after the end of the training period, all subjects will repeat the second and the third sessions.

Intervention: Training (minute oscillation stretching) (Other)

Control group

No Intervention

T2D patients and controls in the control group will not perform any specific training. However, they will participate to the same three sessions as the experimental group.

Outcomes

Primary Outcomes

Muscle and tendon stiffness differences between T2D patients and controls

Time Frame: Data will be collected at baseline (pre-intervention)

Achilles tendon and muscle (gastrocnemius medialis) stiffness (units: Nm/mm) will be evaluated during isometric maximum voluntary contractions. Torque values (units: Nm) will be recorded using a dynamometer (Cybex Norm) whereas tendon elongation (units: mm) and muscle fascicle displacement (units: mm) will be recorded using an ultrasound scanner (MycrusExt, Telemed).

Tendon Stiffness Differences Between T2D Patients and Controls

Time Frame: Data were collected at baseline (pre-intervention)

Achilles tendon stiffness (units: Nm/mm) was evaluated during isometric maximum voluntary contractions. In turn, stiffness was calculated based on the ratio between Torque values (units: Nm), which were recorded using a dynamometer (Cybex Norm), and tendon elongation values (units: mm), which were recorded using an ultrasound scanner (MycrusExt, Telemed).

Secondary Outcomes

  • Effect of training on muscle and tendon stiffness (in patients and controls)(Data will be collected at baseline, immediately after the intervention (10 weeks of training) and 5 weeks after the end of the intervention)
  • Correlation between tissue glycation indicators (AGEs) and muscle-tendon stiffness in T2D patients and controls(Data will be collected at baseline (pre-intervention))
  • Correlation between tissue glycation indicators (RAGE) and muscle-tendon stiffness in T2D patients and controls(Data will be collected at baseline (pre-intervention))
  • Effect of Training on Tendon Stiffness (in Patients)(Data were collected at baseline and immediately after the intervention (10 weeks of training).)
  • Tissue Glycation Indicators (Hb1Ac) in T2D Patients and Controls(Data were collected at baseline (pre-intervention))
  • Tissue Glycation Indicators (RAGE) in T2D Patients and Controls(Data were collected at baseline (pre-intervention))

Investigators

Sponsor
Universita di Verona
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Paola Zamparo

Principal Investigator

Universita di Verona

Study Sites (2)

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