COMPLETED

Examine the Feasibility and Acceptability of Project Support

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

In this study, the investigators will conduct a proof-of-concept pilot trial of delivering the Project Support Positive Parenting Module (Project Support) to n = 30 families waiting for trauma-focused services. Investigators hypothesize that Project Support will be feasible and acceptable as evidenced by benchmarks for recruitment, retention at post assessment, engagement, fidelity, and program satisfaction. Investigators will also explore trends on caregiver emotional support, parenting self-efficacy, and child mental health symptoms.

Official Title

A Brief Intervention to Enhance Supportive Parenting and Treatment Engagement Among Families Waiting for Trauma-Focused Services

Quick Facts

Study Start:2024-07-02
Study Completion:2025-06-03
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06391229

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:5 Years to 12 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. * Family is seeking trauma-focused services for their child as measured by their placement on the waitlist for services at the National Crime Victims Center;
  2. * Child is between 5 - 12 years old;
  3. * Caregiver agreed to be contacted for volunteer research opportunities;
  4. * Caregiver and child can communicate in either English or Spanish;
  5. * Child has been living with caregiver for at the last 6 months or longer;
  6. * Family is able to participate in services delivered via telehealth.
  1. * Child or caregiver has a diagnosis that would impair their ability to participate in or benefit from services (e.g., traumatic brain injury, developmental disability, psychosis);
  2. * Child is in Foster Care or Department of Social Services custody;
  3. * The caregiver is unwilling or unable to give informed consent and/or the child is unwilling and unable to give assent.

Contacts and Locations

Principal Investigator

Caitlin Rancher, PhD
PRINCIPAL_INVESTIGATOR
Medical University of South Carolina

Study Locations (Sites)

National Crime Victims Center
Charleston, South Carolina, 29425
United States

Collaborators and Investigators

Sponsor: Medical University of South Carolina

  • Caitlin Rancher, PhD, PRINCIPAL_INVESTIGATOR, Medical University of South Carolina

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 Date2024-07-02
Study Completion Date2025-06-03

Study Record Updates

Study Start Date2024-07-02
Study Completion Date2025-06-03

Terms related to this study

Keywords Provided by Researchers

  • Non-offending caregiver
  • Child trauma

Additional Relevant MeSH Terms

  • Parent-Child Relations
  • Parenting
  • Child Mental Disorder