RECRUITING

Patient-Reported Outcomes and Quality of Life in Adult and Pediatric Patients With Nodular Lymphocyte-Predominant Hodgkin Lymphoma (NLPHL)

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

There is a pressing need to measure patient-reported symptoms in patients of all ages diagnosed with nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL). This study aims to measure longitudinal symptom burden and treatment tolerability utilizing validated patient-reported outcomes (PROs) instruments. Primary Objective: * To develop the data collection infrastructure required to prospectively collect longitudinal electronic patient-reported outcomes (PROs) survey instruments in adult and pediatric patients diagnosed with NLPHL. Secondary Objective: * To examine differences in baseline and longitudinal changes in PROs based on disease characteristics, disease status, and treatment strategies among adult and pediatric patients diagnosed with NLPHL.

Official Title

A Pilot Study of Prospective Patient-Reported Outcomes and Quality of Life in Adult and Pediatric Patients With Nodular Lymphocyte-Predominant Hodgkin Lymphoma (NLPHL)

Quick Facts

Study Start:2024-04-04
Study Completion:2028-01-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06098430

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:8 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Valerie Crabtree, PhD
CONTACT
866-278-5833
referralinfo@stjude.org
Jessi Rogers Blake, BSN, RN,CCRP
CONTACT
901-595-4108
jessi.rogers-blake@stjude.org

Principal Investigator

Valerie Crabtree, PhD
PRINCIPAL_INVESTIGATOR
St. Jude Children's Research Hospital
Ajay Major, MD, MS
PRINCIPAL_INVESTIGATOR
University of Colorado, Denver
Anna Jones, PhD
PRINCIPAL_INVESTIGATOR
St. Jude Children's Research Hospital
Matthew Rees, MD
PRINCIPAL_INVESTIGATOR
St. Jude Children's Research Hospital
Jamie Flerlage, MD, MS
PRINCIPAL_INVESTIGATOR
University of Rochester

Study Locations (Sites)

University of Colorado Hospital
Aurora, Colorado, 80045
United States
St. Jude Children's Research Hospital
Memphis, Tennessee, 38105
United States

Collaborators and Investigators

Sponsor: St. Jude Children's Research Hospital

  • Valerie Crabtree, PhD, PRINCIPAL_INVESTIGATOR, St. Jude Children's Research Hospital
  • Ajay Major, MD, MS, PRINCIPAL_INVESTIGATOR, University of Colorado, Denver
  • Anna Jones, PhD, PRINCIPAL_INVESTIGATOR, St. Jude Children's Research Hospital
  • Matthew Rees, MD, PRINCIPAL_INVESTIGATOR, St. Jude Children's Research Hospital
  • Jamie Flerlage, MD, MS, PRINCIPAL_INVESTIGATOR, University of Rochester

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 Date2024-04-04
Study Completion Date2028-01-31

Study Record Updates

Study Start Date2024-04-04
Study Completion Date2028-01-31

Terms related to this study

Additional Relevant MeSH Terms

  • Nodular Lymphocyte-Predominant Hodgkin Lymphoma