Childhood Cancer Survivors' Affective Response to Exercise
NCT ID: NCT05763290
Last Updated: 2025-09-19
Study Results
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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RECRUITING
125 participants
OBSERVATIONAL
2023-03-22
2030-02-28
Brief Summary
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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.
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Detailed Description
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The plan for this study is to administer single category implicit association tests (PSC-IAT's) to participants during on campus SJLIFE testing and use this data to determine the feasibility of this tool's use in survivors of childhood cancer without cognitive impairment. This study will also administer the Behavioral Regulations in Exercise Questionnaire (BREQ-2)37 to participants as a construct validity check to the PSC-IAT.
The procedures include PSC-IAT and BREQ-2 tests (before and after strenuous exercise as part of the SJLIFE protocol) and a qualitative interview. These will be in addition to standard components of the SJLIFE on-campus visit.
Conditions
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Study Design
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OTHER
PROSPECTIVE
Interventions
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Affective Response to Exercise
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
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Inclusion Criteria
* 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 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
18 Years
39 Years
ALL
No
Sponsors
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St. Jude Children's Research Hospital
OTHER
Responsible Party
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Principal Investigators
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Megan Ware, MS, PhD
Role: PRINCIPAL_INVESTIGATOR
St. Jude Children's Research Hospital
Deo Srivastava, PhD
Role: PRINCIPAL_INVESTIGATOR
St. Jude Children's Research Hospital
Lisa Jacola, PhD, ABPP-CN2
Role: PRINCIPAL_INVESTIGATOR
St. Jude Children's Research Hospital
Rachel Webster, PhD
Role: PRINCIPAL_INVESTIGATOR
St. Jude Children's Research Hospital
Tara Brinkman, PhD
Role: PRINCIPAL_INVESTIGATOR
St. Jude Children's Research Hospital
Kevin Krull, PhD
Role: PRINCIPAL_INVESTIGATOR
St. Jude Children's Research Hospital
Melissa Hudson, MD
Role: PRINCIPAL_INVESTIGATOR
St. Jude Children's Research Hospital
Leslie Robinson, 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
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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CAREX
Identifier Type: -
Identifier Source: org_study_id
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