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NCT05377008 · ClinicalTrials.gov registry record · NA

Intervention Effectiveness on the Neurocognitive Functioning of Children and Adolescents With Neurofibromatosis Type 1

A NA study, sponsored by Virginia Commonwealth University.

Completed
Registry status
NA
Development phase
38
Enrollment target

NCT05377008 is a NA study that has completed, run by Virginia Commonwealth University. The registered enrollment target is 38 participants.

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The verdict

NCT05377008, a NA study, has completed, sponsored by Virginia Commonwealth University.

COMPLETED
Registry status
NA
Development phase
38 participants
Enrollment target

Study Summary

Children with neurofibromatosis are more likely to have difficulties related to their psychological and neurocognitive functioning (e.g., more likely to have depression, have social difficulties, be diagnosed with ADHD). The purpose of this randomized control study is to determine how effective and useful this study's single session intervention can be in improving psychological and neurocognitive functioning. Enrolled families will consist of one parent/guardian and child. Parents and patients will complete questionnaires and objective tests at baseline, 3 months, and 6 months. Families randomized to the intervention arm will be provided with one single session intervention at Month 1 to learn about their child's testing results and receive psychoeducation and recommendations related to psychological and neurocognitive functioning.

Interventions

  • BEHAVIORAL OPTIMAL-SSI

Trial Details

FieldValue
Enrollment Target 38 participants
Start Date 2022-05-13
Est. Completion 2023-05-05
Phase NA

Sponsor

Virginia Commonwealth University

558 total trials

What the Registry Record Tells You About NCT05377008

The ClinicalTrials.gov registry entry for NCT05377008 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 38 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Virginia Commonwealth University, which has 558 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which OPTIMAL-SSI is the first listed.

NCT05377008 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05377008 about?

NCT05377008 is a clinical study titled "Intervention Effectiveness on the Neurocognitive Functioning of Children and Adolescents With Neurofibromatosis Type 1". Children with neurofibromatosis are more likely to have difficulties related to their psychological and neurocognitive functioning (e.g., more likely to have depression, have social difficulties, be diagnosed with ADHD). The purpose of this randomized control study is to determine how effective and ...

What is the current status of trial NCT05377008?

This trial is currently completed. It is a NA study. The enrollment target is 38 participants. The study started on 2022-05-13. Estimated completion is 2023-05-05.

What interventions are being tested in trial NCT05377008?

The interventions under investigation include: OPTIMAL-SSI (BEHAVIORAL).

Who is sponsoring clinical trial NCT05377008?

This trial is sponsored by Virginia Commonwealth University, which has 558 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.