NCT03090386CompletedNot Applicable
Evaluation of Cognitive-Communication Deficits Following Treatment of Primary Brain Tumor Patients
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Mayo Clinic
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- Cognitive Communication Survey
Study Overview
Brief Summary
This study is to evaluate which cognitive-linguistic symptoms are most commonly experienced following brain tumor treatment. Cognitive surveys will be administered after treatment of primary brain tumor cancer.
Study Design
- Study Type
- Observational
- Observational Model
- Case Only
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to 89 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •be between18 to 89 years old;
- •have undergone at least one cycle of a cancer treatment regimen (e.g., chemotherapy, radiotherapy, surgery)
- •have completed at least one cycle of a cancer treatment regimen within five years of enrollment in the study;
- •be native speakers of American English;
- •have obtained a minimum of a high school education;
- •self-report at least one cognitive-linguistic or social-emotional deficit as assessed by the FACT-BR; and
- •must demonstrate capacity to sign informed consent based on Informed Consent for Research: A Guide to Assessing a Participant's Understanding tool.
Exclusion Criteria
- •are younger than 18 years old or older than 89 years old;
- •have not undergone at least one cycle of a cancer treatment regimen following diagnosis (e.g., chemotherapy, radiotherapy, surgery)
- •have not undergone at least one cycle of a cancer treatment regimen in the five year period prior to enrollment;
- •are not native speakers of American English;
- •have not obtained a minimum of a high school education;
- •do not self-report at least one cognitive-linguistic or social-emotional deficit as assessed by the FACT-BR; or
- •do not demonstrate the capacity to sign informed consent
Outcomes
Primary Outcomes
Cognitive Communication Survey
Time Frame: 1 day at time of consent
Survey is completed at time of consent
Secondary Outcomes
- Cognitive-linguistic Standardized Testing(within 3 months of cognitive communication survey)
- Follow-up Survey(within 6 months after completion of standardized testing)
Investigators
Nadia N. Laack, M.D.
PI
Mayo Clinic
Study Sites (1)
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