Improving Cognition After Cancer

Not Applicable

Active, not recruiting

• Conditions: Breast Cancer Survivors; Cognitive Dysfunction

• Registration Number: NCT04049695
• Lead Sponsor: University of California, San Diego

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2019-8-6
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Active, not recruiting
• Sex: Female
• Target Recruitment: 253

Inclusion Criteria

Inclusion Criteria:<br><br> - breast cancer survivors who have completed active treatment at least 6 months prior<br> to enrollment and are within 5 years of diagnosis of stage 1, 2, or 3 breast cancer<br><br> - self-report difficulties with cognition since their cancer diagnosis<br><br> - self-report low levels of moderate to vigorous physical activity<br><br> - have a Fitbit compatible device with internet<br><br> - breast cancer was treated with chemotherapy and/or hormonal therapy<br><br>Exclusion Criteria:<br><br> - medical condition that could make it potentially unsafe to be in an unsupervised<br> physical activity intervention<br><br> - currently taking tamoxifen or aromatase inhibitor that will be stopped in the next 6<br> months<br><br> - unable to commit to a 12-month study

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
National Institutes of Health Toolbox - Cognition Domain - Oral Symbol Digital Test

Secondary Outcome Measures

Name	Time	Method
National Institutes of Health Toolbox - Cognition Domain - Oral Symbol Digital Test;Patient Reported Outcomes Measurement Information System (PROMIS) cognitive abilities