Characterizing Sleep Among Long-term Survivors of Childhood Cancer

Description

The patients are being asked to take part in this clinical trial because they received cancer treatment as a child at St. Jude. The study comprehensively examines sleep among three distinct diagnostic groups of survivors in the SJLIFE cohort: ALL, CNS tumors, and non-CNS solid tumors. Primary Objective The primary aim of this protocol is to estimate the prevalence of various sleep disorders among long-term survivors of childhood ALL, CNS tumors, and non- CNS solid tumors. Exploratory Objective The exploratory objective of the study is to explore associations between the prevalence of sleep disorders and clinical outcomes collected in SJLIFE.

Conditions

ALL, Adult, CNS Tumor, Solid Tumor

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Study Overview

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Study Details

Study overview

The patients are being asked to take part in this clinical trial because they received cancer treatment as a child at St. Jude. The study comprehensively examines sleep among three distinct diagnostic groups of survivors in the SJLIFE cohort: ALL, CNS tumors, and non-CNS solid tumors. Primary Objective The primary aim of this protocol is to estimate the prevalence of various sleep disorders among long-term survivors of childhood ALL, CNS tumors, and non- CNS solid tumors. Exploratory Objective The exploratory objective of the study is to explore associations between the prevalence of sleep disorders and clinical outcomes collected in SJLIFE.

Characterizing Sleep Among Long-term Survivors of Childhood Cancer

Characterizing Sleep Among Long-term Survivors of Childhood Cancer

Condition
ALL, Adult
Intervention / Treatment

-

Contacts and Locations

Memphis

St. Jude Children's Research Hospital, Memphis, Tennessee, United States, 38105

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Participant in SJLIFE and \> 5 years from diagnosis.
  • * \>18 years of age at time of enrollment.
  • * Diagnosed with ALL (treated with CRT or chemotherapy only) or CNS tumors (posterior fossa tumors or supratentorial tumors) or non-CNS solid tumors (with abdominal or chest radiation or bilateral retinoblastoma survivors).
  • * Participant was less than 21 years of age at time of diagnosis.
  • * Speaks and understands English (polysomnography device speaks to patients only in English).
  • * Remote participant must have Wi-Fi access
  • * Estimated intelligence score \<80.
  • * Currently prescribed an intervention for a sleep disorder.
  • * Survivor of craniopharyngioma.
  • * Survivor of Hodgkin Lymphoma.
  • * Relapsed or treated with hematopoietic stem cell therapy.
  • * Brain injury unrelated to cancer diagnosis or therapy.
  • * Pulmonary injury unrelated to cancer diagnosis or therapy.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

St. Jude Children's Research Hospital,

Kevin Krull, PhD, PRINCIPAL_INVESTIGATOR, St. Jude Children's Research Hospital

Study Record Dates

2025-12