← Back to Clinical Trials
Recruiting NCT05763290

NCT05763290 Childhood Cancer Survivors' Affective Response to Exercise

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT05763290
Status Recruiting
Phase
Sponsor St. Jude Children's Research Hospital
Condition ALL, Childhood
Study Type OBSERVATIONAL
Enrollment 125 participants
Start Date 2023-03-22
Primary Completion 2027-02

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 39 Years
Study Type OBSERVATIONAL
Interventions
Affective Response to Exercise

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 125 participants in total. It began in 2023-03-22 with a primary completion date of 2027-02.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The primary objective of this study is to assess the feasibility of administering the Personalized Single-Category Implicit Association Test (PSC-IAT) to young adult survivors of childhood cancer. Participants will perform a total of three trials of a cognitive task before and after their scheduled SJLIFE cardiovascular stress testing. Participants will then be asked to participate in a qualitative interview about the cognitive task tool and body sensations and emotions experienced during exercise.

Eligibility Criteria

Inclusion Criteria: * Participants enrolled in St. Jude Lifetime Cohort (SJLIFE) aged 18-39 years at completion of on campus visit * Primary diagnosis of acute lymphoblastic leukemia (ALL) * No cranial radiation therapy (CRT) as part of treatment for ALL * Identify as physically inactive (do not meet Centers for Disease Control and Prevention (CDC) guidelines of 150 minutes of moderate physical activity per week or 75 minutes of vigorous physical activity per week) * Women who are not currently pregnant Exclusion Criteria: * Individuals who cannot speak, read, and/or understand English. * Individuals with an estimated IQ of \<70 and/or per PI discretion * Individuals with any contraindication to stress testing (i.e. cardiovascular complications) * Women who are currently pregnant

Contact & Investigator

Central Contact

Megan Ware, MS, PhD

✉ referralinfo@stjude.org

📞 888-226-4343

Principal Investigator

Megan Ware, MS, PhD

PRINCIPAL INVESTIGATOR

St. Jude Children's Research Hospital

Frequently Asked Questions

Who can join the NCT05763290 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 39 Years, studying ALL, Childhood. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05763290 currently recruiting?

Yes, NCT05763290 is actively recruiting participants. Contact the research team at referralinfo@stjude.org for enrollment information.

Where is the NCT05763290 trial being conducted?

This trial is being conducted at Memphis, United States.

Who is sponsoring the NCT05763290 clinical trial?

NCT05763290 is sponsored by St. Jude Children's Research Hospital. The principal investigator is Megan Ware, MS, PhD at St. Jude Children's Research Hospital. The trial plans to enroll 125 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology