Female Concussion Head Cooling
NCT07303933, Not applicable, Not yet recruiting, Penn State University
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Female Concussion Head Cooling | ClinicalTrials.gov |
| NCT number | NCT07303933 | ClinicalTrials.gov |
| Status | Not yet recruiting | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 32 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | Penn State University | ClinicalTrials.gov |
| Conditions | Concussion (Diagnosis), Concussion Post Syndrome, Concussion, Mild | ClinicalTrials.gov |
| Interventions | Brain Cooling | ClinicalTrials.gov |
| First posted | 2025-12-26 | ClinicalTrials.gov |
| Last updated | 2025-12-26 | ClinicalTrials.gov |
Registered outcomes 9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Beck's Depression Inventory-Fast Screen | The metrics will be assessed on pre-intervention (Day 1) and post-intervention (Day 28). | The Beck's Depression Inventory-Fast Screen is a 13-item subjective report of depression symptoms. | ClinicalTrials.gov |
| Primary | HAM-A | The metrics will be assessed pre-intervention (Day 1) and post-intervention (Day 28). | the HAM-A is a 14-item subjective report of anxiety symptoms. | ClinicalTrials.gov |
| Primary | The Penn State Worry Questionnaire | The metrics will be assessed pre-intervention (Day 1) and post-intervention (Day 28). | The Penn State Worry Questionnaire is a 16-item subjective report of perceived worry. | ClinicalTrials.gov |
| Primary | Psychomotor Vigilance Task (PVT) | The metrics will be assessed pre-intervention (Day 1) and post-intervention (Day 28). | The PVT is a very brief (\<1 min) test to assess reaction time and sustained attention. | ClinicalTrials.gov |
| Primary | Dual 2-back Test | The metrics will be assessed pre-intervention (Day 1) and post-intervention (Day 28). | The Dual 2-back Test is a 72 second measure of working memory. | ClinicalTrials.gov |
| Primary | Stroop Task | The metrics will be assessed pre-intervention (Day 1) and post-intervention (Day 28). | The Stroop task is a brief measure of selective attention, processing speed, and executive function | ClinicalTrials.gov |
| Secondary | Consensus Sleep Diary (CSD) | CSD will be recorded daily throughout the intervention (from Day 1 to Day 28). | The CSD is a remote application that allows for description and tracking of metrics related to sleep quantity and quality. | ClinicalTrials.gov |
| Secondary | Clue App | Clue entries will be recorded daily throughout the intervention (from Day 1 to Day 28). | The Clue App is a qualitative journaling tool for recording menstrual cycle timeline and symptom severity. | ClinicalTrials.gov |
| Secondary | Post-Concussion Symptom Scale (PCSS) | PCSS will be recorded daily throughout the intervention (from Day 1 to Day 28). | The PCSS is a 21 item concussion symptom self-scoring measure. Each item ranks a different concussion symptom category on a 0-6 scale. | 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 6
The papers the trial lists on ClinicalTrials.gov.
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 3
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 |
|---|---|---|
| 2-Back Task | Primary outcome | ConductCognition |
| Psychomotor Vigilance Task | 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)