Psycho-Educational Cognition Intervention in Patients With Blood and Lymph Cancer

City of Hope

Status

Withdrawn

Conditions

Hematopoietic and Lymphoid Cell Neoplasm

Treatments

Other: Quality-of-Life Assessment

Other: Survey Administration

Other: Educational Intervention

Study type

Interventional

Funder types

Other

NIH

Identifiers

NCT03804164

18442 (Other Identifier)

NCI-2018-03851 (Registry Identifier)

Details and patient eligibility

About

This pilot trial studies how well a psycho-educational program called Emerging from the Haze works in helping patients with blood and lymph cancer. Sometimes, patients who have undergone treatment for cancer experience thinking or memory problems that make work, school, or everyday life activities, such as grocery shopping, difficult. The Emerging from the Haze program may provide resources to help deal with these types of challenges in patients with blood and lymph cancer.

Full description

PRIMARY OBJECTIVES:

I. Demonstrate feasibility and acceptability for young adult survivors of various cancers utilizing Emerging from the Haze program.

SECONDARY OBJECTIVES:

I. Describe, summarize study population. II. Characterize, compare the measure scores at pre-intervention assessment to the measure scores at post-intervention assessment.

OUTLINE:

Patients participate in the Emerging from the Haze psycho-educational program weekly over 2 hours for 6 weeks.

Sex

All

Ages

18 to 39 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

A diagnosis of a hematological malignancy.
Having received chemotherapy with or without radiation therapy.
Physician approval.
Functional Assessment of Cancer Therapy-Cognition (FACT-COG) score < 59 on the perceived cognitive impairments (PCI) subscale.
Eligible after 2 months (60 +/- 5 days) of completing all their active cancer treatment with the exception of patients that are post-transplant.
Subjective complaint of cognitive concerns at time of enrollment.
Must be able to understand and communicate proficiently in English.
Ability to understand and the willingness to sign a written informed consent.
Agree to complete study surveys.

Exclusion criteria

Patients who have significant personality disorders or unstable psychiatric disorders as assessed by the interviewing clinician.
Patients with known brain metastases, history of brain metastases or radiation to the brain.
Patients with a history of stroke or other pre-existing neurological condition that may contribute to cognitive dysfunction.
Non-English speaking patients.