SarcoImage: Imaging Biomarkers of the Effects of a Mixed Exercise Program

Sponsor
University of Valencia (Other)
Overall Status
Completed
CT.gov ID
NCT03834558
Collaborator
Fundación Universidad Católica de Valencia San Vicente Mártir (Other), Quironsalud (Other)
60
1
2
20.9
2.9

Study Details

Study Description

Brief Summary

The aim is quantify, correlate and establish the diagnostic and prognostic value of the variation of the image biomarkers obtained by magnetic resonance (muscle volume, morphological, biochemical and structural biomarkers) longitudinally in fragile or pre-frail elders with sarcopenia after a mixed physical training of strength and myofascial self-conditioning. This project is based on an, longitudinal, prospective, controlled, randomized, intervention study and blind for the researchers responsible for the study. 60 elderly with sarcopenia and frailty (Intervention Group, n=30; Control Group, n=30) will participate in the study. Intervention Group participants will perform 6-months mixed exercise program consisting in high-intensity strength training and self-myofascial conditioning. Data will be take trough 2 measurements that will be take place at baseline and post-intervention. Criteria of frailty, criteria of sarcopenia, sociodemographic, clinics, kinanthropometric, functional, nutritional and confusing variables will be evaluated. Moreover, magnetic resonance images will be performed to obtain muscle volume, morphological, biochemical and structural biomarkers.

Condition or Disease Intervention/Treatment Phase
  • Other: Mixed exercise program
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
This project is based on an, longitudinal, prospective, controlled, randomized, intervention study and blind for the researchers responsible for the study. Thus, the subjects participating in the study will be divided into 2 groups, one of which will perform the mixed exercise program (intervention group, IG), and another that will follow their daily routine without added exercise (control group, CG). Each group will have 2 measurements in which the corresponding variables will be evaluated: A) before the start of the intervention, B) at 6 months (at the end of the intervention)This project is based on an, longitudinal, prospective, controlled, randomized, intervention study and blind for the researchers responsible for the study. Thus, the subjects participating in the study will be divided into 2 groups, one of which will perform the mixed exercise program (intervention group, IG), and another that will follow their daily routine without added exercise (control group, CG). Each group will have 2 measurements in which the corresponding variables will be evaluated: A) before the start of the intervention, B) at 6 months (at the end of the intervention)
Masking:
Double (Investigator, Outcomes Assessor)
Masking Description:
Investigator: The persons who make the data analysis and decide whether a patient has experienced an outcome of interest will be masked. Outcome assessors: The persons who assess patients and provide outcome data will be masked.
Primary Purpose:
Treatment
Official Title:
SarcoImage: Anatomical and Physiological Validation by Magnetic Resonance Imaging Biomarkers of the Effects of High Intensity Strenght Training and Myofascial Self-conditioning on Sarcopenia in Frail and Prefrail Elderly
Actual Study Start Date :
Feb 6, 2019
Actual Primary Completion Date :
Apr 15, 2020
Actual Study Completion Date :
Nov 2, 2020

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control Group

They will follow their daily routine without added exercise

Experimental: Intervention Group

They will perform the mixed exercise program

Other: Mixed exercise program
A progressive program of high intensity strength and myofascial conditioning will be carried out in 2 non-consecutive weekly sessions (24 weeks). Each session will include: A) Warm up on a cycle ergometer B) Strength circuit: 6 exercises will be included to strengthen different muscle groups (2 in the upper extremities, 2 in the trunk and 2 in the lower extremities). 3 sets of 10-15 repetitions until the failure. The load will be set to 70% of 1 maximal resistance. C) Self-myofascial conditioning: 10 repetitions, in the direction of the fibres of each muscle group, with different materials. 7 muscle groups will be worked (quadriceps, hamstrings, abductors, gluteus, pectoralis, full back and trapezius). D) At the end, static stretches will be performed

Outcome Measures

Primary Outcome Measures

  1. Muscle volume [6 months]

    Changes related to macroscopic changes in muscle tissue assessed by magnetic resonance after a 6-month program of high intensity training and myofascial self-conditioning, specifically muscle volume of the thigh by compartment - anterior, medial and posterior (in ml)

  2. Bone volume [6 months]

    Changes related to macroscopic changes in bone tissue assessed by magnetic resonance after a 6-month program of high intensity training and myofascial self-conditioning, specifically relative volume of bone (in %)

  3. Relative volume of intramuscular fat [6 months]

    Changes related to macroscopic changes in fat tissue assessed by magnetic resonance after a 6-month program of high intensity training and myofascial self-conditioning, specifically relative volume of intramuscular fat (in %)

  4. Extramuscular subcutaneous fat [6 months]

    Changes related to macroscopic changes in fat tissue assessed by magnetic resonance after a 6-month program of high intensity training and myofascial self-conditioning, specifically extramuscular subcutaneous fat (in ml)

  5. Microscopic fat fraction [6 months]

    Changes related to microscopic changes in fat tissue assessed by magnetic resonance after a 6-month program of high intensity training and myofascial self-conditioning, specifically microscopic fat fraction (in %)

  6. Descriptors of muscle texture [6 months]

    Changes related to microscopic changes in muscle tissue assessed by magnetic resonance after a 6-month program of high intensity training and myofascial self-conditioning, specifically statistical descriptors of muscle texture: energy, entropy, contrast and homogeneity (adimensional)

  7. Diffusion coefficient [6 months]

    Changes related to microscopic changes in diffusion coefficient assessed by magnetic resonance after a 6-month program of high intensity training and myofascial self-conditioning, specifically diffusion coefficient and apparent diffusion coefficient (mm2/s)

Secondary Outcome Measures

  1. Body muscle mass [6 months]

    Changes produced by 6-month program of high intensity training and myofascial self-conditioning on body muscle mass (kg/m2) measured according to criteria of sarcopenia of European Working Group of Sarcopenia in Older People.

  2. Handgrip strength [6 months]

    Changes produced by 6-month program of high intensity training and myofascial self-conditioning on handgrip strength (kg) measured according to criteria of sarcopenia of European Working Group of Sarcopenia in Older People.

  3. Walking speed [6 months]

    Changes produced by 6-month program of high intensity training and myofascial self-conditioning on walking speed (m/s) measured according to criteria of sarcopenia of European Working Group of Sarcopenia in Older People.

  4. Body mass index [6 months]

    Changes on body mass index (measured in kg/m2) generated by 6-month program of high intensity training and myofascial self-conditioning

  5. Lean mass [6 months]

    Changes on lean impedance (measured in % by bioimpedance) generated by 6-month program of high intensity training and myofascial self-conditioning

  6. Fat mass [6 months]

    Changes on fat impedance (measured in % by bioimpedance) generated by 6-month program of high intensity training and myofascial self-conditioning

  7. Body perimeters [6 months]

    Changes on calf and thigh perimeter (measured in cm) generated by 6-month program of high intensity training and myofascial self-conditioning

  8. Articular range [6 months]

    Changes on range of joint movement of coxofemoral and knee articulation (measured in degrees) generated by 6-month program of high intensity training and myofascial self-conditioning

  9. Perceived pain [6 months]

    Changes on pain (measured by visual analogic scale, 0 to 10 points, higher values = worse outcome) generated by 6-month program of high intensity training and myofascial self-conditioning

  10. Activities of daily living [6 months]

    Changes in functionality and independence measured by Barthel Index (0 to 100 points, < 60 dependence, higher values = better outcome) produced by 6-month program of high intensity training and myofascial self-conditioning

  11. Functional and physical performance [6 months]

    Changes in functional and physical performance measured by Short Physical Performance Battery (0 to 12 points, higher score = higher function) produced by 6-month program of high intensity training and myofascial self-conditioning

  12. Forced spirometry [6 months]

    Changes in respiratory function, measured by forced spirometry parameters assessed with a spirometer, produced by 6-month program of high intensity training and myofascial self-conditioning

  13. Respiratory muscles strength [6 months]

    Changes in respiratory pressures generated in mouth by respiratory muscles (assessed with a respiratory pressure gauge) produced by 6-month program of high intensity training and myofascial self-conditioning

  14. Perceived quality of life [6 months]

    Changes produced by 6-month program of high intensity training and myofascial self-conditioning related to quality of life (EuroQol 5 Dimensions - 3 levels Index, 0 to 1 points, higher values = better outcome)

  15. Type of drugs used [6 months]

    Type and dose of drugs consumed before and after a 6-month program of high intensity training and myofascial self-conditioning

Eligibility Criteria

Criteria

Ages Eligible for Study:
70 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients of both genders,

  • aged 70 years old or more,

  • with habitual residence in Valencia,

  • with independent wandering (they can have technical aids, but not from someone else)

  • that meets Fried's pre-frailty or frailty criteria

  • EGWSOP's sarcopenia criteria

  • who has agreed to participate in the study and signed the informed consent

Exclusion Criteria:
  • Patients with life expectancy less than six months

  • Institutionalized patients

  • Patients with severe visual or auditory deficits

  • Patients with contraindication in the performance of physical exercise (cardiovascular risk factors)

  • Patients with contraindications for the magnetic resonance study, especially carriers of non-compatible pacemakers, neurostimulators, cochlear implants and intracranial aneurysm clamping.

  • Patients with severe psychiatric illness or moderate or severe cognitive impairment.

  • Patients who refuse to sign the informed consent.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Valencia - Faculty of Physiotherapy Valencia Spain 46009

Sponsors and Collaborators

  • University of Valencia
  • Fundación Universidad Católica de Valencia San Vicente Mártir
  • Quironsalud

Investigators

  • Principal Investigator: Francisco Martinez Arnau, PhD, Universitat de Valencia
  • Study Director: Roberto Sanz Requena, PhD, Hospital QuironSalud - Hospital Universitario La Fe (GIBI)
  • Study Director: Ana Pablos Monzó, PhD, Fundación Universidad Católica de Valencia
  • Study Director: Pilar Pérez-Ros, PhD, Fundación Universidad Católica de Valencia

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Francisco Martínez Arnau, Martínez-Arnau FM, PT, PhD, University of Valencia
ClinicalTrials.gov Identifier:
NCT03834558
Other Study ID Numbers:
  • H1488746567568
First Posted:
Feb 8, 2019
Last Update Posted:
Nov 3, 2020
Last Verified:
Nov 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Francisco Martínez Arnau, Martínez-Arnau FM, PT, PhD, University of Valencia
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 3, 2020