Investigating Memory and Physical Activity After Cancer Treatment in Survivors of Adolescent and … (NCT06880861) | Clinical Trial Compass
RecruitingNot Applicable
Investigating Memory and Physical Activity After Cancer Treatment in Survivors of Adolescent and Young Adult Cancers
United States150 participantsStarted 2025-07-01
Plain-language summary
This study evaluates relationships among physical activity, thinking, and memory after cancer treatment in survivors of adolescent and young adult cancers.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1This study is focusing on memory and thinking skills in young adult cancer survivors — given my specific diagnosis and treatment history, does my doctor think my cognitive function is something worth monitoring right now?
2Since this trial isn't testing a new drug or treatment but is looking at the relationship between physical activity and cognitive performance after cancer, what would actually be expected of me in terms of time, tasks, or activity levels if I were to participate?
3The study uses something called a Stroop task to measure cognitive performance — can my doctor explain what that test involves and whether my current cognitive symptoms, if any, are the kind this study is designed to track?
4Because this is listed as Phase NA, meaning it's an observational or behavioral study rather than a drug trial, can my doctor help me understand whether joining this kind of research could interfere with or complement any active treatment I'm still receiving?
5Are there standard clinical tools or follow-up programs already available through my care team to monitor memory and cognitive changes after my cancer treatment, and how would those compare to what this study is offering?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.