NCT02914067Recruiting
Cognitive Biomarkers in Pediatric Brain Tumor Patients
Source: ClinicalTrials.gov · Last updated 21 Nov 2025
Brief summary (registry, in English)
The investigators will focus on three cohorts of brain tumor patients aged, 4-18 years, to answer two critical questions: 1) Can the investigators acquire high quality data relevant to cognitive function during the peri-diagnostic period and, 2) can the investigators develop predictive models for cognitive outcomes using serial examination of functional imaging and cognitive function. Any patient with a newly diagnosed brain tumor aged 4-18 will be eligible for enrollment in cohort 1. Only patients with previously diagnosed tumors of the posterior fossa will be eligible for cohort 2. For cohort 3, eligible patients will include patients with a clinical diagnosis of posterior fossa syndrome with physical impairments that prohibit completion of the NIH Toolbox Cognitive Battery. The investigators have decided to expand the eligible tumor types to better capture the most significant deficit variability that can be caused by tumors outside the posterior fossa. Thus, this focus will provide a platform to analyze the impact that different tumor types and different standard treatments have on cognitive dysfunction. The rationale for inclusion of subjects on cohort 3 is that posterior fossa syndrome is one of the most cognitively devastating diagnoses following a posterior fossa surgery. The causes of posterior fossa syndrome and unknown and there are currently no interventions to improve symptoms. RsfcMRI would offer a novel and non-invasive assessment of posterior fossa syndrome patients by assessing connectivity within and outside of the cerebellum. Expanding the tumor eligibility will allow us to further explore the effect tumor location will have on cognitive testing and rsfcMRI. Here, repeated evaluations on and off therapy will provide the necessary data points to establish trajectories of cognitive development and recovery in this population.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 200 (estimated)
- First submitted
- 19 Sept 2016
- Start date
- 26 Oct 2016
- Primary completion date
- 30 Nov 2026
- Lead sponsor
- Washington University School of Medicine
- Diseases
- Childhood cancers
- NCT number
- NCT02914067
What you commit to
- Study type: Interventional
- Planned participants: 200
- From 26 Oct 2016 to the primary completion date, 30 Nov 2026
- 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.
Prior treatment
- Previous diagnosis of a posterior fossa brain tumor
- Contraindication to MRI scan (i.e. due to cardiac pacemaker)
- Cohort 4 (50 Patients will be enrolled to Cohort 4. This will include patients previously enrolled on Cohorts 1-3 above.)
Other illness
- Presence of visual impairment to an extent that the patient is unable to complete the computer testing
- Contraindication to MRI scan (i.e. due to cardiac pacemaker)
- Presence of visual impairment to an extent that the patient is unable to complete the computer testing
- Contraindication to MRI scan (i.e. due to cardiac pacemaker)
- Cohort 3 (20 patients will be enrolled to this cohort. This may include some or all of the patients enrolled to Cohort 1) Inclusion Criteria
- Clinical diagnosis of post-operative posterior fossa syndrome
Age
- Between 4 and 18 years of age, inclusive
Other
- Programmable Shunt
- Cohort 2 (150 patients will enrolled to this cohort. This may include some or all of the patients enrolled to Cohort 1.)
- Inability to complete NIH Toolbox
- Life expectancy of at least one year
- Able to understand and willing to consent assent to the research proposed, along with consent of legal guardian(s) if applicable
- Contraindiciation to MRI scan (i.e. due to cardian pacemaker)
- Presence of dental braces or programmable shunt
- Patient requires sedation for MRI scan
Who the study is looking for
- Between 4 and 18 years of age, inclusive
- Newly diagnosed primary brain tumor of any location and any histology
- Life expectancy of at least one year
- Able to understand and willing to consent or assent to the research proposed, along with consent of legal guardian(s) if applicable
- Between 4 and 18 years of age, inclusive
- Previous diagnosis of a posterior fossa brain tumor; patients who are either undergoing active treatment for posterior fossa tumor or who have completed treatment will be eligible for study enrollment
- Life expectancy of at least one year
- Able to understand and willing to consent assent to the research proposed, along with consent of legal guardian(s) if applicable
- Between 12-30 years of age, inclusive
- Diagnosis of a brain tumor \>3 years prior to study enrollment
- Life expectancy of at least one year
- Able to understand and willing to consent assent to the research proposed, along with consent of legal guardian(s) if applicable
- Patient must be able to complete a 1 hour MRI scan without sedation
Criteria the registry did not label
- Cohort 1 (30 patients will be enrolled to this cohort)
Age in the registry: 4 years to 18 years · Sex: All · Does not accept 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 |
|---|---|---|---|
| Washington University School of Medicine Coordinator of this site? Confirm its status | St Louis | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.