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COMPLETED NA

Efficacy of Computerized Cognitive Training and Stimulant Medication in Neurofibromatosis Type 1

NCT02944032 · View on ClinicalTrials.gov ↗

Study Summary

The main objective of the study is to assess the efficacy of a home-based, computerized cognitive training (CT) program, called CogmedRM, targeted to improve working memory in children with NF1 and working memory difficulties. This is a Phase II randomized parallel group controlled clinical trial comparing two interventions on cognitive outcomes. Participants will be stratified by stimulant medication use and randomized equally between the two interventions within stratum. Participants will be in the study for to 11 weeks.

Conditions Studied

Interventions

  • OTHER CogmedRM
  • OTHER Mobymax

Study Locations (1)

District of Columbia

  • Children's National Health System — Washington D.C.

Trial Details

FieldValue
Enrollment Target 103 participants
Start Date 2016-05
Est. Completion 2021-09-27
Phase NA

Sponsor

Kristina Hardy

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02944032

The ClinicalTrials.gov registry entry for NCT02944032 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 103 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Kristina Hardy, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Neurofibromatosis Type 1 appearing as the primary indexed condition, and to 2 interventions — of which CogmedRM is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02944032 reports 1 study location spanning 1 distinct geographic area — top geographies include District of Columbia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02944032 about?

NCT02944032 is a clinical study titled "Efficacy of Computerized Cognitive Training and Stimulant Medication in Neurofibromatosis Type 1". The main objective of the study is to assess the efficacy of a home-based, computerized cognitive training (CT) program, called CogmedRM, targeted to improve working memory in children with NF1 and working memory difficulties. This is a Phase II randomized parallel group controlled clinical trial co...

What is the current status of trial NCT02944032?

This trial is currently completed. It is a NA study. The enrollment target is 103 participants. The study started on 2016-05. Estimated completion is 2021-09-27.

What conditions does trial NCT02944032 study?

This clinical trial studies the following conditions: Neurofibromatosis Type 1. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02944032?

The interventions under investigation include: CogmedRM (OTHER), Mobymax (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02944032?

This trial is sponsored by Kristina Hardy, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02944032 being conducted?

This trial has 1 study location across District of Columbia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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