NRG-CC011

Temporarily Closed to Accrual

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Protocol Information

Tab containing protocol details, study design, and eligibility criteria
Tab containing study documents, informed consent forms, and study materials
Tab containing information for potential study participants

Cognitive Training For Cancer Related Cognitive Impairment In Breast Cancer Survivors: A Multi-Center Randomized Double-Blinded Controlled Trial

Principal Investigator

Diane Von Ah

Status

Temporarily Closed to Accrual

Open to Accrual

February 2, 2024

Temporarily Closed to Accrual

May 9, 2025


Disease Site

Symptom Management [CC] Other

Phase

III

Developmental Therapeutics

No

Primary Objective

This Phase III trial will examine the efficacy of computerized cognitive training methods on perceived cognitive impairment in breast cancer survivors.

Patient Population

Stage I-III, non-metastatic breast cancer survivors who are 18 years of age or older and are 6 months to 5 years post-treatment with cancer-related cognitive impairment (CRCI) .

Target Accrual

386

Protocol Documents

Available via the National Cancer Institute (NCI) Cancer Trials Support Unit (CTSU) website.


Patient Study Webpage

To learn more about this study, visit the Patient Study Webpage.