ACTIVE_NOT_RECRUITING

Patient- Generated Health Data to Predict Childhood Cancer Survivorship Outcomes

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Some childhood cancer survivors have health problems as the result of previous cancer treatment. This study is being done to determine if we can better predict the risk a childhood cancer survivor might have for developing future health issues. The goal of this study is to enable regular monitoring of patient-generated health data (PGHD), including symptoms, physical activity, energy expenditure, sleep behavior and heart rate variability, and utilize these data in predicting survivor-specific risk of late effects to improve survivorship care and outcomes.

Official Title

Patient- Generated Health Data to Predict Childhood Cancer Survivorship Outcomes

Quick Facts

Study Start:2023-03-20
Study Completion:2028-06-20
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05342155

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.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * ≥18 years of age at the time of study
  2. * Enrolled on SJLIFE
  3. * ≥5 years from initial diagnosis of pediatric cancer/malignancy
  4. * Currently not receiving cancer therapies
  5. * Access to web-enabled smartphone
  1. * Known severe neurocognitive impairment (e.g., estimated intelligence score \[FSIQ\] \<70), which requires proxies to complete daily symptom and PRO surveys;
  2. * \<3rd-grade reading level or not able to communicate in English;
  3. * Currently pregnant or reports planning to become pregnant in the next two years;
  4. * Lack of access to web-enabled smartphone, or not able to use/access internet from the device.

Contacts and Locations

Principal Investigator

I-Chang Huang, PhD
PRINCIPAL_INVESTIGATOR
St. Jude Children's Research Hospital

Study Locations (Sites)

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

Collaborators and Investigators

Sponsor: St. Jude Children's Research Hospital

  • I-Chang Huang, PhD, PRINCIPAL_INVESTIGATOR, St. Jude Children's Research Hospital

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-03-20
Study Completion Date2028-06-20

Study Record Updates

Study Start Date2023-03-20
Study Completion Date2028-06-20

Terms related to this study

Keywords Provided by Researchers

  • Health Data

Additional Relevant MeSH Terms

  • Survivorship
  • Childhood Cancer