RECRUITING

Testing eSCCIP: An eHealth Psychosocial Intervention for English and Spanish Speaking Parents of Children With Cancer

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

It is critical to provide accessible evidence-based psychosocial support to parents and caregivers of children with cancer (PCCC) in order to mitigate individual and family-level psychosocial risks. This effectiveness trial evaluates an eHealth intervention for English- and Spanish-speaking (PCCC) with study endpoints focused on decreasing negative psychosocial sequelae (acute distress, posttraumatic stress, and anxiety) and improving coping abilities (coping self-efficacy, cognitive coping strategies). The long-term goal of this research program is to sustain and disseminate an effective, scalable, high-reach, and cost-effective intervention to provide crucial support to PCCC across the pediatric cancer trajectory.

Official Title

A Randomized Controlled Trial of eSCCIP: An eHealth Psychosocial Intervention for English and Spanish Speaking Parents of Children With Cancer

Quick Facts

Study Start:2023-04-14
Study Completion:2026-06-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05294302

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:Not specified
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Participants must be the parent or primary caregiver of a child (ages 0 - 18 years old) diagnosed with cancer.
  2. * Participants must be able to speak and read English or Spanish.
  3. * Participants must have access to the internet through a computer or mobile device (e.g., smartphone, tablet).
  1. * PCCC are ineligible to participate if their child is not expected to live longer than six months from the time of potential recruitment

Contacts and Locations

Study Contact

Kimberly Canter, Ph.D.
CONTACT
3026514501
kimberly.canter@nemours.org

Study Locations (Sites)

Children's Hospital Los Angeles
Los Angeles, California, 90027
United States
Nemours Children's Health, Delaware
Wilmington, Delaware, 19803
United States
MD Anderson Cancer Center
Houston, Texas, 77030
United States

Collaborators and Investigators

Sponsor: Nemours Children's Clinic

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 Date2023-04-14
Study Completion Date2026-06-30

Study Record Updates

Study Start Date2023-04-14
Study Completion Date2026-06-30

Terms related to this study

Keywords Provided by Researchers

  • eHealth
  • pediatric cancer
  • parents
  • psychosocial intervention

Additional Relevant MeSH Terms

  • Pediatric Cancer