Investigating the Inverted-U Relationship Between Cognitive Performance and Plasma Epinephrine
NCT05407259, Not applicable, Unknown, National Taiwan Normal University
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Investigating the Inverted-U Relationship Between Cognitive Performance and Plasma Epinephrine | ClinicalTrials.gov |
| NCT number | NCT05407259 | ClinicalTrials.gov |
| Status | Unknown | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 40 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | National Taiwan Normal University | ClinicalTrials.gov |
| Conditions | Healthy Young Adults | ClinicalTrials.gov |
| Interventions | Resistance exercise | ClinicalTrials.gov |
| First posted | 2022-06-07 | ClinicalTrials.gov |
| Last updated | 2022-06-09 | ClinicalTrials.gov |
Registered outcomes 13
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Inhibitory control (change between baseline and 5 minutes after intervention/control) | Baseline (before intervention) and 5 minutes after (post-task) intervention/control. | The Inhibitory control (Stroop interference score) will be the mean incongruent reaction time minus the mean congruent reaction time. Lower scores mean a better outcome. | ClinicalTrials.gov |
| Primary | Inhibitory control (change between baseline and 20 minutes after intervention/control) | Baseline (before intervention) and 20 minutes after (post-task) intervention/control. | The Inhibitory control (Stroop interference score) will be the mean incongruent reaction time minus the mean congruent reaction time. Lower scores mean a better outcome. | ClinicalTrials.gov |
| Primary | Inhibitory control (change between baseline and 35 minutes after intervention/control) | Baseline (before intervention) and 35 minutes after (post-task) intervention/control. | The Inhibitory control (Stroop interference score) will be the mean incongruent reaction time minus the mean congruent reaction time. Lower scores mean a better outcome. | ClinicalTrials.gov |
| Primary | Inhibitory control (change between baseline and 50 minutes after intervention/control) | Baseline (before intervention) and 50 minutes after (post-task) intervention/control. | The Inhibitory control (Stroop interference score) will be the mean incongruent reaction time minus the mean congruent reaction time. Lower scores mean a better outcome. | ClinicalTrials.gov |
| Primary | Information processing speed (change between baseline and 5 minutes after intervention/control) | Baseline (before intervention) and 5 minutes after intervention/control. | The Information processing speed will be the mean simple reaction time. Lower scores mean a better outcome. | ClinicalTrials.gov |
| Primary | Information processing speed (change between baseline and 20 minutes after intervention/control) | Baseline (before intervention) and 20 minutes after intervention/control. | The Information processing speed will be the mean simple reaction time. Lower scores mean a better outcome. | ClinicalTrials.gov |
| Primary | Information processing speed (change between baseline and 35 minutes after intervention/control) | Baseline (before intervention) and 35 minutes after intervention/control. | The Information processing speed will be the mean simple reaction time. Lower scores mean a better outcome. | ClinicalTrials.gov |
| Primary | Information processing speed (change between baseline and 50 minutes after intervention/control) | Baseline (before intervention) and 50 minutes after intervention/control. | The Information processing speed will be the mean simple reaction time. Lower scores mean a better outcome. | ClinicalTrials.gov |
| Secondary | Epinephrine (change between baseline and immediately after intervention/control) | Baseline and immediately after intervention/control. | Plasma epinephrine concentrations will be measured in duplicate using a commercially available enzyme-linked immunosorbent assay (ELISA) kit. | ClinicalTrials.gov |
| Secondary | Epinephrine (change between baseline and 15 minutes after intervention/control) | Baseline and 15 minutes after intervention/control. | Plasma epinephrine concentrations will be measured in duplicate using a commercially available enzyme-linked immunosorbent assay (ELISA) kit. | ClinicalTrials.gov |
| Secondary | Epinephrine (change between baseline and 30 minutes after intervention/control) | Baseline and 30 minutes after intervention/control. | Plasma epinephrine concentrations will be measured in duplicate using a commercially available enzyme-linked immunosorbent assay (ELISA) kit. | ClinicalTrials.gov |
| Secondary | Epinephrine (change between baseline and 45 minutes after intervention/control) | Baseline and 45 minutes after intervention/control. | Plasma epinephrine concentrations will be measured in duplicate using a commercially available enzyme-linked immunosorbent assay (ELISA) kit. | ClinicalTrials.gov |
| Secondary | Epinephrine (change between baseline and 60 minutes after intervention/control) | Baseline and 60 minutes after intervention/control. | Plasma epinephrine concentrations will be measured in duplicate using a commercially available enzyme-linked immunosorbent assay (ELISA) kit. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Grants 0
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.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 2
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 | Source |
|---|---|---|
| Simple Reaction Time | Primary outcome | ConductCognition |
| Stroop Color-Word Test | Primary outcome | ConductCognition |
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)