Status:

COMPLETED

Feasibility of the Memory and Attention Adaptation-Training Geriatrics Intervention in Older Cancer Survivors With Mild Cognitive Impairment

Lead Sponsor:

Allison Magnuson

Collaborating Sponsors:

National Institute on Aging (NIA)

Conditions:

Cognitive Dysfunction

Eligibility:

All Genders

65+ years

Phase:

NA

Brief Summary

Cancer-related cognitive dysfunction (CRCD) affects up to 75% of patients receiving chemotherapy and older adults are at greater risk of developing CRCD, which can negatively affect their functional i...

Detailed Description

Cancer-related cognitive dysfunction (CRCD) affects up to 75% of patients receiving chemotherapy and older adults are at greater risk of developing CRCD, which can negatively affect their functional i...

Eligibility Criteria

Inclusion

  • Inclusion Criteria:
  • Be age 65 or older
  • Able to provide informed consent. All patients will be assessed using the University of California, San Diego Brief Assessment of Capacity to Consent (UBACC)56 - a score \>14.5 will define ability to independently provide informed consent. For patients scoring \<14.5, or if investigators have additional concerns, we will require that their health care proxy participate in the consenting process and sign an informed consent and patients will required to provide assent.
  • Able to read and understand English
  • Have a prior diagnosis of cancer and completed curative intent chemotherapy. Patients are permitted to be receiving maintenance therapy (e.g. endocrine therapy) in the adjuvant setting.
  • Have a clinical diagnosis of MCI, a score \<26 on the Montreal Cognitive Assessment (MOCA), or a score \<18 on the Montreal Cognitive Assessment-BLIND (MOCA-BLIND). If the patient had a MOCA evaluation completed as a part of routine clinical care in the preceding 3 months prior to consent date, this may be used for eligibility purposes.
  • Be independent in Activities of Daily Living (ADL)

Exclusion

    Key Trial Info

    Start Date :

    December 10 2021

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    July 26 2023

    Estimated Enrollment :

    12 Patients enrolled

    Trial Details

    Trial ID

    NCT05258058

    Start Date

    December 10 2021

    End Date

    July 26 2023

    Last Update

    July 10 2024

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    University of Rochester

    Rochester, New York, United States, 14642