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Spots Global Cancer Trial Database for MAAT For Young Adult Cancer Survivors

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Trial Identification

Brief Title: MAAT For Young Adult Cancer Survivors

Official Title: Modifying Memory and Attention Adaptation Training (MAAT) For Young Adult Childhood Cancer Survivors

Study ID: NCT06150976

Conditions

Cancer

Interventions

MAAT-YS

Study Description

Brief Summary: The goal of this clinical trial is to pilot-test a modified version of telehealth-delivered Memory and Attention Adaption Training (MAAT) that is tailored to young adult childhood cancer survivors (ages 18-39; MAAT-YS) with cancer-related cognitive impairment (CRCI). MAAT-YS consists of 8 weekly visits (45-minutes in duration) and participants use a survivor workbook and complete homework between visits. Participants in this single-group pilot trial (N=9) will complete online self-report measures of cognitive symptoms, quality of life, treatment satisfaction and a brief online neuropsychological test battery at baseline and post-MAAT-YS timepoints.

Detailed Description: The goal of this clinical trial is to pilot-test a modified version of telehealth-delivered Memory and Attention Adaption Training (MAAT) that is tailored to young adult childhood cancer survivors (ages 18-39; MAAT-YS) with cancer-related cognitive impairment (CRCI). MAAT-YS consists of 8 weekly visits (45-minutes in duration) and participants use a survivor workbook and complete homework between visits. This pilot trial will determine MAAT-YS feasibility, treatment satisfaction and size of effect in self-report and objective measures of neurocognitive function. Eligible participants will be 9 individuals who were diagnosed with non-central-nervous system (CNS) cancer (including leukemia/lymphoma without known CNS involvement) prior to the age of 18, are at least 1-year from completion of cancer treatment, including chemotherapy. Participants will complete online self-report measures of cognitive symptoms, quality of life, treatment satisfaction and a brief online neuropsychological test battery at baseline and post-MAAT-YS timepoints. If successful, further research is planned with a larger, multi-site randomized controlled trial of MAAT-YS.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Indiana University School of Medicine, Indianapolis, Indiana, United States

University of Pittsburgh School of Medicine/UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania, United States

St. Jude Children's Research Hospital, Memphis, Tennessee, United States

Contact Details

Name: Robert J Ferguson, PHD

Affiliation: UPMC Hillman Cancer Center/University of Pittsburgh School of Medicine

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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