Trial · NCT07189130
The Acute Effect of Different Resistance Exercise Loads on Irisin and Brain-derived Neurotrophic Factor in Blood Serum and Plasma
NCT07189130, Not applicable, Active not recruiting, University of Ljubljana
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. The Acute Effect of Different Resistance Exercise Loads on Irisin and Brain-derived Neurotrophic Factor in Blood Serum and Plasma. Trials, record NCT07189130. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07189130
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- The Acute Effect of Different Resistance Exercise Loads on Irisin and Brain-derived Neurotrophic Factor in Blood Serum and Plasma
- NCT number
- NCT07189130
- Status
- Active not recruiting
- Phases
- Not applicable
- Enrollment
- 24 participants, estimated
- Lead sponsor
- University of Ljubljana
- Conditions
- BDNF, Irisin, Resistance Exercise, Stroop Test, Lactate, Healthy Young Adult
- Interventions
- Exercise: 80% 1 RM with 2 minutes break, Exercise: 80% 1RM with1 minute break, Exercise: accenuated eccentric exercise, Control
- First posted
- 2025-09-23
- Last updated
- 2025-12-16
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | plasma BDNF | pre, 5 minutes post exercise, 1 hour post exercise, 3 hours post exercise. | BDNF will be determined in blood plasma with ELISA kit. |
| Primary | Irisin | pre, 5 minutes post exercise, 1 hour post exercise, 3 hours post exercise. | Irisin will be measured in blood plasma. |
| Primary | serum BDNF | pre, 5 minutes post exercise, 1 hour post exercise, 3 hours post exercise. | BDNF will be determined in blood serum with ELISA kit. |
| Primary | Platelet count | pre, 5 minutes post exercise, 1 hour post exercise, 3 hours post exercise. | Platelet count in blood will be done. |
| Primary | BDNF per platelet | pre, 5 minutes post exercise, 1 hour post exercise, 3 hours post exercise. | The amount of BDNF per platelet will be calculated. |
| Secondary | Lactate | pre, 5 minutes post exercise, 1 hour post exercise, 3 hours post exercise. | Lactate will be measured in blood. |
| Secondary | Stroop test | pre, 15 minutes post exercise. | Stroop test will be used as an assessment of cognitive functions. The number of read word will be assessed. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests1
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as |
|---|---|
| Stroop Color-Word Test | Secondary outcome |
Source ConductCognition
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07189130
GET https://conductscience.org/api/trials/v1/NCT07189130/registered