Effects of Computer-Assisted Cognitive Rehabilitation Programs With Breast Cancer Survivors

Status unconfirmed · Not applicable

Conditions studied: Cognitive Impairment, Breast Cancer

In brief

Potential study participants will be recruited at breast cancer survivor support groups. Informed consent will be obtained with a form approved by the TWU IRB and participants will complete 4 tests. Then participants will be randomly assigned to one of two computer-assisted cognitive programs. Participants will be sent by email, exercises specific to their assigned computer-assisted cognitive program from Happyneuron Pro (http://ie.scientificbraintrainingpro.eu/). Cognitive training on the computer entails 30 minutes a day, five times a week for one month. At the end of the study, the four pretests will be repeated, a satisfaction survey administered.

Key facts

Study ID

NCT04027400

Run by

Texas Woman's University

People needed

52

Starts

2018-02-26

Expected to finish

2020-02-26

Last updated by the study team

2019-08-13

Who can join

Age: 18 and older, up to 99. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• study participant self-identifies as breast cancer survivor
• had treatment that may have included surgery, chemotherapy, radiation, pharmacological or any combination of these treatments
• participant states has cognitive problems due to cancer treatment

You may not qualify if…

• persons who cannot read or understand spoken English
• have disorders that may affect their cognition including major mental disorder, central nervous system disorders, Alzheimer's disease, dementia, developmental delay, traumatic brain injury, or cerebrovascular accident.

Where it is running

• Texas Woman's University — Houston, Texas, United States (enrolling)

Full record on ClinicalTrials.gov

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