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Improving Cognition After Cancer (ICAN)

University of California San Diego logo

University of California San Diego

Status

Active, not recruiting

Conditions

Breast Cancer Survivors
Cognitive Dysfunction

Treatments

Behavioral: Exercise
Behavioral: Control

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This study will test whether a physical activity intervention can improve cognition in breast cancer survivors and help the development of physical activity guidelines for cognition in breast cancer survivors.

Full description

Many breast cancer survivors experience problems with mental abilities such as memory, attention, and concentration (known as cognition). Increasing physical activity has been shown to improve cognition in adults; however, little is known about whether this is helpful for cancer survivors as well. This study will test whether a physical activity intervention can improve cognition in breast cancer survivors and help the development of physical activity guidelines for cognition in breast cancer survivors.

Enrollment

253 patients

Sex

Female

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • breast cancer survivors who have completed active treatment at least 6 months prior to enrollment and are within 5 years of diagnosis of stage 1, 2, or 3 breast cancer
  • self-report difficulties with cognition since their cancer diagnosis
  • self-report low levels of moderate to vigorous physical activity
  • have a Fitbit compatible device with internet
  • breast cancer was treated with chemotherapy and/or hormonal therapy

Exclusion criteria

  • medical condition that could make it potentially unsafe to be in an unsupervised physical activity intervention
  • currently taking tamoxifen or aromatase inhibitor that will be stopped in the next 6 months
  • unable to commit to a 12-month study

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

253 participants in 2 patient groups

Exercise Intervention
Experimental group
Description:
This arm will receive a 12-month individually tailored phone and email-based exercise program.
Treatment:
Behavioral: Exercise
Health & Wellness Intervention
Active Comparator group
Description:
This arm will receive a 12-month health and wellness program.
Treatment:
Behavioral: Control

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Lindsay Dillon, MPH; Hava Barkai

Data sourced from clinicaltrials.gov

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