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Recruiting NCT06880861

Investigating Memory and Physical Activity After Cancer Treatment in Survivors of Adolescent and Young Adult Cancers

— Observational Hematopoietic and Lymphatic System Neoplasm Malignant Solid Neoplasm

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Non-Interventional Study.
Who it may be relevant to
Registry conditions: Hematopoietic and Lymphatic System Neoplasm, Malignant Solid Neoplasm. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

This study evaluates relationships among physical activity, thinking, and memory after cancer treatment in survivors of adolescent and young adult cancers.

Interventions

  • Other Non-Interventional Study
    Non-Interventional Study

Primary outcome measures

  • Cognitive performance on Stroop task [Time frame: Up to 4 weeks]
Secondary outcome measures (9)
  • Cognitive performance on Visual Memory Test [Time frame: 2 weeks]
  • Cognitive performance on Verbal Memory Test [Time frame: 2 weeks]
  • Cognitive performance on Symbol Digit Coding Test [Time frame: 2 weeks]
  • Cognitive performance on Shifting Attention Test [Time frame: 2 weeks]
  • Cognitive performance on Continuous Performance Test [Time frame: Up to 4 weeks]
  • Cognitive performance on Reasoning Test [Time frame: 2 weeks]
  • Cognitive performance on Four Part Continuous Performance Test [Time frame: 2 weeks]
  • Self-reported cognition - FACT-COG [Time frame: 2 weeks]
  • Average weekly minutes of physical activity [Time frame: 2 weeks]

Eligibility criteria

Inclusion criteria

  • Adults (aged 18+ years)
  • Primary diagnosis of cancer when 15-39 years-old
  • Access to a desktop computer or laptop with reliable internet access
  • No gross motor impairments that prohibit ambulation
  • Willing to complete study requirements
  • English speaking

Exclusion criteria

  • Diagnosed with nonmelanoma skin cancer only
  • Not diagnosed with cancer in adolescent and young adult (AYA) age range of 15-39 years
  • Scheduled travel during the study period that is not indicative of individual's normal schedule

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

United States · 1 center
  • Mayo Clinic in Arizona — Scottsdale

Identifiers

NCT: NCT06880861 · 24-008654 · NCI-2025-01193 · 24-008654

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗