Cognitive Intervention at the End of Therapy for Survivors of Childhood ALL Treated on TOTXVI

NCT ID: NCT03187977

Last Updated: 2022-03-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-08-03

Study Completion Date

2021-10-13

Brief Summary

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Computer-based cognitive training has been found to be helpful for improving attention and working memory in pediatric and adult patients with existing cognitive difficulties. A previous study was conducted at St. Jude Children's Research Hospital with survivors of childhood cancer who were experiencing difficulties with attention and/or working memory. Findings from that study indicated that the use of Cogmed, computer-based cognitive training, is effective in improving attention and working memory in survivors.

Researchers want to learn whether Cogmed intervention completed at the end of therapy for acute lymphoblastic leukemia will be effective for all survivors (i.e., regardless of whether they have existing difficulties).

PRIMARY OBJECTIVES:

* To evaluate the overall participation rate in a randomized, standard-of-care controlled trial of computerized cognitive intervention administered at the end of TOTXVI therapy.
* To estimate the study completion rate in a randomized, standard-of-care controlled trial of computerized cognitive intervention administered at the end of TOTXVI therapy.
* To estimate the compliance rate for participants randomized to the intervention arm of a computerized cognitive intervention administered at the end of TOTXVI therapy.
* To estimate the standard deviation for the overall cohort on a measure of working memory.
* To use neuroimaging data collected in the context of the Total Therapy XVI trial to explore candidate biomarkers predictive of response to the computerized cognitive intervention.

Detailed Description

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Participants enrolled on the TOTXVI protocol at SJCRH will be randomized to either complete the Cogmed intervention at the end of their therapy, or to a standard-of-care condition.

Cogmed is a computer-based cognitive training program that consists of rotating exercises that train attention and working memory. The exercises are presented in a child-friendly, game-like format. Training is completed at home in 25 sessions for 15-45 minutes each weekday for 5-9 weeks. A research team member serves as a coach who monitors progress and provides support through weekly phone calls with study participants and their parents/guardians. Information regarding compliance and performance is tracked over the internet and used to tailor feedback during weekly telephone coaching.

Neurocognitive assessments will be conducted at baseline, immediate-post (3-4 months after baseline), and 8 month follow-up (12 months after baseline).

Conditions

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Acute Lymphoblastic Leukemia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Participants will be randomized to either the intervention group to receive cognitive training or to the standard of care group who will not receive cognitive training.
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Outcome Assessors
The study examiner (clinical research assistants or psychological examiners) will not know which group of participants is associated with each arm.

Study Groups

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Cognitive Training

Participants will participate in computer-based cognitive training at the end of therapy.

Group Type ACTIVE_COMPARATOR

Cognitive training

Intervention Type BEHAVIORAL

Cogmed is a computer-based cognitive training program that consists of rotating exercises that train attention and working memory. The exercises are presented in a child-friendly, game-like format. The program is completed at home for 15-45 minutes each weekday for 5-9 weeks.

Standard-of-Care

At the end of therapy, participants will participate in the current standard-of-care which does not include computer-based cognitive training.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Cognitive training

Cogmed is a computer-based cognitive training program that consists of rotating exercises that train attention and working memory. The exercises are presented in a child-friendly, game-like format. The program is completed at home for 15-45 minutes each weekday for 5-9 weeks.

Intervention Type BEHAVIORAL

Other Intervention Names

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Cogmed

Eligibility Criteria

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Inclusion Criteria

* Currently enrolled and receiving treatment for acute lymphoblastic leukemia (ALL) on the TOTXVI therapy protocol at St. Jude Children's Research Hospital
* At least 4 years of age at the time of randomization
* Primary language is English
* Parent/legal guardian/caregiver that speaks English available to assist in participant's training

Exclusion Criteria

* Significant cognitive impairment as determined by either an IQ of ≤ 70 or by clinician judgment
* Major sensory or motor impairment that would preclude valid cognitive testing
* Major psychological condition that would preclude completion of the intervention
* History of significant CNS injury or disease predating or unrelated to cancer diagnosis
* Documented ADHD predating cancer diagnosis
Minimum Eligible Age

4 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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St. Jude Children's Research Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Lisa M. Jacola, PhD

Role: PRINCIPAL_INVESTIGATOR

St. Jude Children's Research Hospital

Locations

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St. Jude Children's Research Hospital

Memphis, Tennessee, United States

Site Status

Countries

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United States

Related Links

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http://stjude.org

St. Jude Children's Research Hospital

http://stjude.org/protocols

Clinical Trials Open at St. Jude

Other Identifiers

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NCI-2017-01276

Identifier Type: REGISTRY

Identifier Source: secondary_id

ALLCOG

Identifier Type: -

Identifier Source: org_study_id

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