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Childhood Cancer Survivors' Affective Response to Exercise

St. Jude Children's Research Hospital logo

St. Jude Children's Research Hospital

Status

Enrolling

Conditions

ALL, Childhood
Acute Lymphoblastic Leukemia

Treatments

Other: Affective Response to Exercise

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Full description

Researchers at St. Jude Children's Research Hospital want to learn about the measurement of implicit association bias towards or against exercise in childhood cancer survivors. Additionally, researchers want to learn more about the physical and emotional experience of exercise from our survivors.

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.

Enrollment

125 estimated patients

Sex

All

Ages

18 to 39 years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

1

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Central trial contact

Kirsten Ness, PhD; Megan Ware, MS, PhD

Data sourced from clinicaltrials.gov

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