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RECRUITING
NCT06747910
NA

Assessment of Remote Approaches for Identification of Autonomic Dysfunction Among Survivors of Leukemia and Lymphoma

Sponsor: St. Jude Children's Research Hospital

View on ClinicalTrials.gov

Summary

This study seeks to determine if diagnosing cardiac autonomic dysfunction (AD) can be done remotely with the same accuracy as in-person testing. If so, the identification of AD could happen sooner, facilitating remote studies of the condition and potentially reducing the risk of illness. Childhood cancer survivors, particularly survivors of acute lymphoblastic leukemia (ALL) and Hodgkins's lymphoma (HL), appear to be at increased risk for AD. Primary Objectives: * To determine the sensitivity and specificity of heart rate variability (HRV), measured remotely with biosensor technology (Actigraph LEAP), compared to in-person assessment using the Ewing battery as the reference standard to identify cardiac autonomic dysfunction (AD) among survivors of leukemia and lymphoma. * To determine the sensitivity and specificity of the Composite Autonomic Symptom Scale 31 (COMPASS31) compared to the Ewing battery to identify AD among leukemia and lymphoma survivors.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

188

Start Date

2025-02-03

Completion Date

2026-06

Last Updated

2026-03-09

Healthy Volunteers

No

Interventions

OTHER

Exercise Intervention - Ewing Battery Assessment

Undergo in-person Ewing battery assessment

OTHER

Questionnaire Administration

Receive COMPASS31 questionnaire

DEVICE

Medical Device Usage and Evaluation

Wear biosensensor heart monitor that remotely collects heart rate variability.

Locations (1)

St. Jude Children's Research Hospital

Memphis, Tennessee, United States