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Utility and Validity of a High-intensity, Intermittent Exercise Protocol

U

University Ghent

Status

Completed

Conditions

Fatigue

Treatments

Other: Fatigue protocol

Study type

Interventional

Funder types

Other

Identifiers

NCT04531891
BC-07679

Details and patient eligibility

About

The purpose of this study is to identify an exercise-induced fatigue protocol to mimic central and peripheral acute fatigue effects associated with participation in vigorous dynamic sports activities and to understand the expected central (cardiovascular) and peripheral (muscular) impact of this protocol.

Full description

Fatigue-related parameters (BORG, heart rate, blood lactate level, concentric/eccentric force of the quadriceps muscle) will be measured before and after different short-term high-intensity, intermittent exercise protocols.

Enrollment

20 patients

Sex

Male

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Men
  • ≥ 18 years
  • Volley- and basketball, non-elite
  • ≥ 3 times per week sports participation
  • No acute or overuse low back/lower extremity injuries in the past 6 months

Exclusion criteria

  • Women
  • <18 years
  • >45 years
  • other sports than volley- and basketball
  • elite players
  • <3 times per week sports participation
  • acute or overuse low back/lower extremity injuries in the past 6 months

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

20 participants in 2 patient groups

All-out, high-intensity, intermittent exercise protocol
Experimental group
Treatment:
Other: Fatigue protocol
5 min, high-intensity, intermittent exercise protocol
Experimental group
Treatment:
Other: Fatigue protocol

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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