Cognitive Rehabilitation Following Breast Cancer Treatment

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age20-75
SponsorUniversity of Missouri-Columbia

About this trial

The goal of this proposed project is to evaluate the feasibility and preliminary effect of metacognitive strategy training to improve activity performance, cognition, and quality of life in breast cancer survivors with cancer-related cognitive impairment (CRCI). The other goal of this proposed project is to examine the effects of CO-OP on resting (rsFC)- and task-state functional connectivity as compared to an inactive control group.

Eligibility criteria

Qualifiers

self-reported CRCI (Global Rating of Cognition dysfunction as "Moderately" "Strongly "or "Extremely" AND a Cognitive Failures Questionnaire1 (CFQ) score >30)

completed treatment for active cancer diagnosis (invasive ductal or lobular BrCA Stages I, II, or III) at least 6 months but not greater than 3 years prior to participation

able to read, write, and speak English fluently

able to provide valid informed consent

Disqualifiers

prior cancer diagnoses of other sites with evidence of active disease within the past year

active diagnoses of any acute or chronic brain-related neurological conditions that can alter normal brain anatomy or function (e.g., Parkinson's disease, dementia, cerebral infarcts) dementia symptoms as indicated by a score of <23 on the Montreal Cognitive Assessment (MoCA)

severe depressive symptoms (Personal Health Questionnaire-9 (PHQ-9) score of ≥21)

history of severe traumatic brain injury, prolonged loss of consciousness (e.g., coma)

Trial design

Treatments tested in this trial

  • Metacognitive Strategy Training (MCST)
  • Inactive Control Group

Treatment groups

50 Participants
are divided into 2 treatment groups

Sponsors and collaborators

University of Missouri-Columbia

Lead sponsor

National Institutes of Health (NIH)

Collaborator

National Cancer Institute (NCI)

Collaborator