Feasibility and Efficacy of rTMS in Healthy Persons
NCT04074811, Not applicable, Withdrawn, Wayne State University
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Feasibility and Efficacy of rTMS in Healthy Persons | ClinicalTrials.gov |
| NCT number | NCT04074811 | ClinicalTrials.gov |
| Status | Withdrawn | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 0 participants, actual | ClinicalTrials.gov |
| Lead sponsor | Wayne State University | ClinicalTrials.gov |
| Conditions | Executive Dysfunction, Pain, Mood | ClinicalTrials.gov |
| Interventions | Repetitive Transcranial Magnetic Stimulation (rTMS) | ClinicalTrials.gov |
| First posted | 2019-08-30 | ClinicalTrials.gov |
| Last updated | 2023-04-13 | ClinicalTrials.gov |
Registered outcomes 8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Stroop Task (cognitive control) | Change from pre- to 25-minutes post-rTMS stimulation in each session | Examine the effect of rTMS stimulation on cognitive control as measured by the Stroop Color-Word task. | ClinicalTrials.gov |
| Primary | Stop Signal Task (impulsivity) | Change from pre- to 15-minutes post-rTMS stimulation in each session | Examine the effect of rTMS stimulation on impulsivity as measured by the Stop Signal Task. | ClinicalTrials.gov |
| Primary | Pain Sensitivity | Change from pre- to 50-minutes post-rTMS stimulation in each session | Examine the effect of rTMS stimulation on pain sensitivity as measured by thermal quantitative sensory threshold (QST) testing. | ClinicalTrials.gov |
| Primary | Delay Discounting Task (cognitive control) | Change from pre- to 10-minutes post-rTMS stimulation in each session | Examine the effect of rTMS stimulation on cognitive control as measured by the brief (2-min) monetary delay discounting task | ClinicalTrials.gov |
| Secondary | Effort Choice Task (motivation) | Change from pre- to 30-minutes post-rTMS stimulation in each session | Examine the effect of rTMS stimulation on behavioral responding as measured by the Effort Choice Task (number of responses on progressive ratio vs. fixed ratio schedules of reinforcement). | ClinicalTrials.gov |
| Secondary | Mood | Change from pre- to 5-minutes post-rTMS stimulation in each session | Examine the effect of rTMS stimulation on mood state as measured by the Positive and Negative Affect Schedule. | ClinicalTrials.gov |
| Secondary | Peripheral Biomarkers | Change from pre- to 0-minutes post-rTMS stimulation in each session | Examine the effect of rTMS stimulation on peripheral biomarkers as measured by the plasma concentrations (ng/ml) of brain derived neurotrophic factor (BDNF) and prolactin. | ClinicalTrials.gov |
| Secondary | Monetary Incentive Delay Task (motivation) | Change from pre- to 40-minutes post-rTMS stimulation in each session | Examine the effect of rTMS stimulation on behavioral responding as measured by the Monetary Incentive Delay Task | 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 4
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 |
|---|---|---|
| Delay Discounting | Primary outcome | ConductCognition |
| Stop-Signal Task | Primary outcome | ConductCognition |
| Stroop Color-Word Test | Primary outcome | ConductCognition |
| Monetary Incentive Delay | Secondary 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)