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Spots Global Cancer Trial Database for Assessment of Cognitive Function in Breast Cancer and Lymphoma Patients Receiving Chemotherapy

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Trial Identification

Brief Title: Assessment of Cognitive Function in Breast Cancer and Lymphoma Patients Receiving Chemotherapy

Official Title: Assessment of Cognitive Function in Breast Cancer and Lymphoma Patients Receiving Chemotherapy at Pre-Treatment, Post-Treatment, at Six Month Follow-Up, and Long-Term Follow-Ups

Study ID: NCT01382082

Interventions

Study Description

Brief Summary: Cognitive impairments in cancer patients represent an important clinical problem. Studies to date estimating prevalence of difficulties in memory, executive function, and attention deficits have been limited by small sample sizes and many have lacked healthy control groups. More information is needed on promising biomarkers and allelic variants that may help to determine the etiology of impairment, identify those most vulnerable to impairment, and develop interventions for these difficulties. This is a longitudinal observational study of cognitive function in breast cancer and lymphoma patients receiving chemotherapy to better understand the prevalence of cognitive difficulties (i.e., problems with memory, executive function, and attention) in these populations.

Detailed Description:

Eligibility

Minimum Age: 21 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: Yes

Locations

Delaware/Christiana Care NCORP, Newark, Delaware, United States

Delaware/Christiana Care NCORP (CHRISTIANA), Newark, Delaware, United States

Heartland, Decatur, Illinois, United States

Kansas City Clinical Oncology Program, Prairie Village, Kansas, United States

Wichita NCORP, Wichita, Kansas, United States

Wichita, Wichita, Kansas, United States

Gulf South MU-NCORP, New Orleans, Louisiana, United States

Cancer Research Consortium of West Michigan, Grand Rapids, Michigan, United States

CRCWM, Grand Rapids, Michigan, United States

Metro Minnesota NCORP, Minneapolis, Minnesota, United States

Metro Minnesota Community Oncology Research Consortium, Saint Louis Park, Minnesota, United States

CCOP - Nevada Cancer Research Foundation, Las Vegas, Nevada, United States

Nevada, Las Vegas, Nevada, United States

Hem Onc CNY, East Syracuse, New York, United States

Kansas City, Rochester, New York, United States

University of Rochester Cancer Center, Rochester, New York, United States

Novant Health Cancer Institute - Kernersville, Winston-Salem, North Carolina, United States

Southeast Clinical Oncology Research Program, Winston-Salem, North Carolina, United States

Columbus NCORP, Columbus, Ohio, United States

Columbus, Columbus, Ohio, United States

Dayton Community Oncology Program, Dayton, Ohio, United States

Dayton, Dayton, Ohio, United States

Pacific Cancer Research Consortium Ncorp, Portland, Oregon, United States

PCRC, Portland, Oregon, United States

NCORP of the Carolinas, Greenville, South Carolina, United States

Upstate Carolina, Spartanburg, South Carolina, United States

Northwest (Virginia Mason), Seattle, Washington, United States

Wisconsin NCORP, Marshfield, Wisconsin, United States

Aurora NCORP, Milwaukee, Wisconsin, United States

Contact Details

Name: Michelle C. Janelsins, PhD

Affiliation: University of Rochester

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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