Cognitive Training Intervention and Attitudes Towards Genetics

Part of paid clinical trials in Birmingham, Alabama.

Sponsor
University of Alabama at Birmingham
Study ID
NCT03094026
Status
Recruiting

Conditions

  • Cognitive Impairment
  • Hematologic Neoplasms
  • Hematopoietic Cell Transplant

Eligibility Criteria

Sex
ALL
Age
21 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Lumosity — BEHAVIORAL
    Computer-based online cognitive training program using the Lumosity cognitive training program.
  • Lumosity (waitlist control) — BEHAVIORAL
    Computer-based online cognitive training program using the Lumosity cognitive training program. The control group will receive the intervention after a waiting period of 12 weeks.

Study Details

A pilot study to evaluate feasibility of enrollment of patients in an intervention to improve neurocognitive function in hematopoietic cell transplantation (HCT) survivors using the cognitive training Lumosity program. In addition, patients' interest in receiving information regarding genetic risk of cognitive impairment post-HCT will be measured.

Key Dates

Start date
Aug 21, 2017
Status verified
Apr 2026
Primary completion
Jul 31, 2027
Completion
Jul 31, 2027

Study Design

Enrollment
60 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE

Arms

  • Experimental: Intervention
    The arm will begin the Lumosity program at enrollment in the study.
  • Active Comparator: Wait List Control
    The arm will begin the Lumosity program 3 months after enrollment in the study.

Primary Outcome Measure

Number of HCT patients completing the 2-arm wait-listed randomized trial of cognitive training intervention for a period of 3 months [ Time Frame: 12 weeks ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
University of Alabama at BirminghamBirminghamAlabama35233
Noha Sharafeldin, MD, MSc, PhD
2056382144
Lindsey Hageman, MPH, CCRP
2056382139

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