MedPath

Human TECAR on Exercise Preconditioning and Post-exercise Recovery

Not Applicable
Recruiting
Conditions
Exercise Recovery
Registration Number
NCT06938984
Lead Sponsor
University of Nove de Julho
Brief Summary

TECAR therapy (Transfer of Energy Capacitive and Resistive) is a type of diathermy that uses radiant energy to generate endogenous heat. However, to the date there are no studies investigating the effects of TECAR therapy on exercise preconditioning and post-exercise recovery in humans. Therefore, the aim of this project is to assess the effects of different treatment protocols of TECAR therapy on. exercise preconditioning and post-exercise recovery in humans

Detailed Description

Fifty male healthy volunteers will be enrolled in a randomized, double-blind (participants and assessors), controlled trial. Volunteers will be allocated in 5 groups of 10 participants each: 1 - Sham-control (fake intervention - massaging with one of the Human TECAR probes with the device turned off before or after the eccentric exercise protocol depending on randomization); 2 - Capacitive mode before exercise (preconditioning); 3 - Resistive mode before exercise (preconditioning); 4 - Capacitive mode after exercise (recovery); and 5 - Resistive mode after exercise (recovery). The treatment target will be the knee extensors muscles (quadriceps).

A standardized knee extension eccentric exercise protocol performed in the isokinetic dynamometer (Biodex System 4) will be used in order to exercise induce skeletal muscle fatigue and damage.

Volunteers will be treated with Human TECAR in a single treatment session, with 10 minutes length, that will be carried out immediately before or immediately after the exercise protocol according to the randomization.

Recruitment & Eligibility

Status
RECRUITING
Sex
Male
Target Recruitment
50
Inclusion Criteria
  • Physically active male participants;
  • Do not present a history of musculoskeletal injury in the regions of the hips, knees and calves in the month preceding the study;
  • Are not using pharmacological agents;
  • Voluntarily commit to participate in all stages of the study.
Exclusion Criteria
  • Present musculoskeletal or joint injuries during data collection;
  • Present history of musculoskeletal injury in the regions of the hips, knees and calves in the month preceding the study.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Change in muscle strength48 hours after eccentric exercise

The muscle strength will be measured through isokinetic dynamometry

Secondary Outcome Measures
NameTimeMethod
Change in muscle strength5 minutes after the treatment, 5 minutes, 1 hour, 24 hours, 72 hours, and 96 hours after the eccentric exercise protocol

The muscle strength will be measured through isokinetic dynamometry

Change in CK activity5 minutes after the treatment, 5 minutes, 1 hour, 24 hours, 72 hours, and 96 hours after the eccentric exercise protocol

The CK activity will be analyzed from the blood samples collected from the participants through biochemical analysis and using specific reagent kits.

Delayed onset muscle soreness - DOMS5 minutes after the treatment, 5 minutes, 1 hour, 24 hours, 72 hours, and 96 hours after the eccentric exercise protocol

DOMS will be assessed through the VAS scale

Temperature5 minutes after the treatment, 5 minutes, 1 hour, 24 hours, 72 hours, and 96 hours after the eccentric exercise protocol

Thigh temperature will be assessed through Thermography using the WellVu camera.

Muscular oxygen saturation index5 minutes after the treatment, 5 minutes, 1 hour, 24 hours, 72 hours, and 96 hours after the eccentric exercise protocol

It will be measured using near-infrared spectroscopy (NIRS)

Muscular blood flow5 minutes after the treatment, 5 minutes, 1 hour, 24 hours, 72 hours, and 96 hours after the eccentric exercise protocol

It will be measured analyzing total hemoglobin in muscle tissue using near-infrared spectroscopy (NIRS)

Muscular effort perception5 minutes after the treatment, 5 minutes, 1 hour, 24 hours, 72 hours, and 96 hours after the eccentric exercise protocol

The CR-100 Effort Perception Scale will be used

Participant satisfaction with the treatment96 hours after the eccentric exercise protocol

The Likert scale will be used

Trial Locations

Locations (1)

Laboratory of Phototherapy and Innovative Technologies in Health

🇧🇷

São Paulo, SP, Brazil

© Copyright 2025. All Rights Reserved by MedPath