NCT06209528Completed
Assessing Neurophysiological and Cognitive Function in School Children
Assessing Neurophysiological Function, Cognitive Function, and Health-related Quality of Life in School Children: a Feasibility Study
Source: ClinicalTrials.gov · Last updated 28 Aug 2024
Brief summary (registry, in English)
This trial will investigate the feasibility of implementing our novel assessment battery in a neurodiverse pediatric population. More specifically, we want to assess our processes and procedures with respect to 1) recruitment rate (i.e., efficiency of our recruitment methods), 2) tolerability (i.e., proportion of participants able to wear the hardware without difficulty), 3) compliance (i.e., proportion of participants able to complete each task as instructed), 4) efficiency (i.e., time to completion of the test battery), and 5) data fidelity (i.e., proportion of test acquisitions with data suitable for subsequent analyses).
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 17 (actual)
- First submitted
- 8 Jan 2024
- Start date
- 26 Mar 2024
- Primary completion date
- 28 Mar 2024
- Lead sponsor
- Life University
- NCT number
- NCT06209528
What you commit to
- Study type: Observational
- Participants enrolled: 17
- From 26 Mar 2024 to the primary completion date, 28 Mar 2024
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Unable to perform the assessments due to contraindications (e.g., has a disorder that causes fainting during postural changes such as POTS or orthostatic hypotension)
- Pacemaker or known heart condition that influences the electrical function of the heart
Other
- Unable to perform assessments due to movement limitations (e.g., confined to a wheelchair)
- Deemed to be at "high risk" of suicide per the C-SSRS
Who the study is looking for
- 5-17 years old
- Student of the Chippewa Falls school district
- Parent(s)/Guardian(s) provide signed informed consent
- Child able to provide signed informed assent \& acknowledge desire to participate verbally (e.g., "Yes, I want to do the study") and/or physically (e.g., nods head \& gives thumbs up).
Age in the registry: 5 years to 17 years · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Chippewa Falls Area Unified School District Coordinator of this site? Confirm its status | Chippewa Falls | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.