ClinicalTrials.Veeva

Menu

The Acute Effect of Different Resistance Exercise Loads on Irisin and Brain-derived Neurotrophic Factor in Blood Serum and Plasma

U

University of Ljubljana

Status

Active, not recruiting

Conditions

Healthy Young Adult
Stroop Test
Irisin
Lactate
Resistance Exercise
BDNF

Treatments

Other: Control
Other: Exercise: 80% 1RM with1 minute break
Other: Exercise: accenuated eccentric exercise
Other: Exercise: 80% 1 RM with 2 minutes break

Study type

Interventional

Funder types

Other

Identifiers

NCT07189130
0120-222/2024-2711-3

Details and patient eligibility

About

The aim of this study is to investigate different resistance training loads on BNDF and irisin levels in platelets, blood serum and plasma.

Full description

In this study, the investigators will examine how three resistance training protocols acutely affect BDNF levels (in serum, plasma, platelet count, and BDNF per platelet) and irisin levels in blood (plasma). The resistance training protocols will differ in intensity, rest intervals between sets and repetition execution. Blood samples will be collected from participants at four time points: before the start of the protocol, 5 minutes after completion of the final set, 1 hour after completion of the final set, and 3 hours after completion of the final set. In addition, blood lactate levels will be monitored at the same time points. Heart rate will also be recorded (immediately before the start of the protocol and 30 seconds after completion of the final set). A control protocol will also be implemented, in which blood will be collected at the same time points. Data will be collected across five visits to the kinesiology laboratory at the University of Ljubljana, Faculty of Sport. Each visit will last approximately 4 hours, except for the first visit where 1RM will be measured.

Enrollment

24 estimated patients

Sex

Male

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • males between 18 and 30 years
  • moderate level of physical activity assessed with IPAQ

Exclusion criteria

  • injuries
  • cardiovascular diseases
  • respiratory diseases
  • psychiatric diseases
  • metabolic diseases
  • other neurodegenerative diseases

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

24 participants in 1 patient group

Intervention: participants going through exercising or control
Experimental group
Description:
All participants will do 1 control protocol and 3 resistance exercises protocols. Order of protocols will be randomized.
Treatment:
Other: Exercise: 80% 1 RM with 2 minutes break
Other: Exercise: accenuated eccentric exercise
Other: Exercise: 80% 1RM with1 minute break
Other: Control

Trial contacts and locations

1

Loading...

Central trial contact

Sara Moškon

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems