Skip to main content
Clinical Trials/NCT04889755
NCT04889755
Completed
Not Applicable

SibACCESS: Developing a Telehealth Intervention to Address Unmet Psychosocial Needs of Siblings of Children With Cancer

Boston University Charles River Campus1 site in 1 country6 target enrollmentFebruary 1, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Siblings
Sponsor
Boston University Charles River Campus
Enrollment
6
Locations
1
Primary Endpoint
Child Posttraumatic Stress Disorder Symptom Scale for DSM-5
Status
Completed
Last Updated
last year

Overview

Brief Summary

This study aims to address barriers to psychosocial care for siblings of children with cancer by piloting a group-based telehealth program for adolescent siblings of youth with cancer. The pilot trial will be preceded by a treatment development stage during which study staff will interview English- and Spanish-speaking families and psychosocial providers to assess preferences for program content, format, timing, and cultural feasibility and acceptability, while considering ideas to minimize participation barriers. Information from interviews will inform any revisions to the proposed pilot program. Then, the new SibACCESS program will be tested with a small group of families located in Massachusetts, Delaware, or Rhode Island using video-teleconferencing technology. Families will complete exit interviews to assess program acceptability and perceived benefits.

Detailed Description

Background: Prolonged, complicated, and intensive pediatric cancer treatment regimens challenge and disrupt the entire family. Siblings of youth with cancer are a psychosocially at-risk and underserved group. Siblings frequently report strong negative emotions, disruptions to family life, poorer academic functioning, more school absenteeism (school-aged siblings), and riskier health behaviors and poorer health outcomes than comparisons (adult siblings). Approximately one-quarter of siblings meet diagnostic criteria for cancer-related posttraumatic stress disorders. Outcomes are worse for siblings from under-represented minority groups and those with fewer socioeconomic resources. Additionally, siblings report low social support and indicate a strong desire to connect with other siblings. The need for sibling support is well established, as outlined in the recently developed evidence- and consensus-based Standards for Psychosocial Care for Children with Cancer and Their Families. Unfortunately, the Sibling Standard is among those least likely to be met within pediatric oncology programs nationwide. SibACCESS Program Description: SibACCESS (Acceptance, Coping, Communication, Engagement, and Social Support) targets the proposed mechanisms of sibling difficulties. The primary goal is to increase siblings' exposure and opportunities to process cancer-related cues to decrease the onset or intensification of posttraumatic stress (PTS). Treatment targets include emotional acceptance, treatment involvement, family communication (via between-session assignments), and social support (fostered by the group format). SibACCESS is based on acceptance-based cognitive-behavioral frameworks, drawing primarily on trauma-focused CBT (TF-CBT). TF-CBT is a structured, short-term treatment that incorporates cognitive-behavioral approaches to promote recovery from trauma. It is a logical starting point for the present study for multiple reasons: (a) TF-CBT was developed specifically for children and adolescents; parent participation is recommended but not required; (b) it has been tested in a group format and using telehealth; (c) it has demonstrated effectiveness across cultural groups; and (d) it is appropriate for youth who meet diagnostic criteria for PTSD and those with sub-clinical PTS. TF-CBT has not yet been evaluated in the context of childhood cancer and may require some adaptations. Thus, SibACCESS also includes skills from Dialectical and Behavioral Therapy (i.e., self-validation of emotions, mindfulness, radical acceptance) to better address distress tolerance and acceptance of the aspects of cancer that are beyond siblings' control. SibACCESS sessions will be facilitated remotely using Zoom. The intervention includes one pre-recorded parent webinar, one brief orientation meeting (sibling and parent), seven weekly sibling group sessions, one individual sibling session, and one individual parent session. The 30-minute parent webinar will provide a program overview, psychoeducation, and brief skills training. Parents will be given "discussion starter" questions to facilitate communication throughout the program. Sibling group sessions are 75 minutes and will include an ice breaker, review of last week's homework (except first session), introduction of new topics, interactive practice of new skills, and assignment of home practice (except final session). Exposure to cancer-related emotions and cues will be emphasized throughout the program, including talking about cancer, confronting cancer-related thoughts and emotions, selecting several individualized cancer-related exposures, and crafting a sibling narrative.

Registry
clinicaltrials.gov
Start Date
February 1, 2023
End Date
June 10, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Boston University Charles River Campus
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 2 or more children in the family (i.e., child with cancer and \>1 sibling)
  • Sibling(s) and child with cancer each under the age of 18 at the time of cancer diagnosis
  • Sibling(s) can be biologically-related, step-siblings, foster-siblings, or adopted-siblings
  • Parent and sibling(s) fluent in English
  • Sibling(s) 12-17 years of age
  • Sibling report of at least mild posttraumatic stress (score \>11 on the Child Posttraumatic Stress Scale for DSM-5)
  • Child with cancer must have received cancer diagnosis at least 3 months prior to the family's enrollment in the study

Exclusion Criteria

  • A cognitive impairment that would interfere with pilot program and interview completion (as reported by parent)
  • Bereavement
  • Significant externalizing behaviors that would interfere with group participation (as reported by parent)

Outcomes

Primary Outcomes

Child Posttraumatic Stress Disorder Symptom Scale for DSM-5

Time Frame: Within 2 weeks post-intervention, data were collected over a period of up to 4 weeks

The Child PTSD Symptom Scale for DSM-5 (CPSS-V) \[citation\] is a 27-item measure of posttraumatic stress. Strong test-retest reliability, internal consistency, and convergent validity with other child PTSD measures have been established. This survey was administered only to sibling participants. Measure was scored by a total summation, scores may range from 0 to 80. \*Higher scores reflect higher levels of post-traumatic stress symptoms

Secondary Outcomes

  • Strengths & Difficulties Questionnaire (SDQ)(Within 2 weeks post-intervention, data were collected over a period of up to 4 weeks)
  • Sibling Perception Questionnaire (SPQ)(Within 2 weeks post-intervention, data were collected over a period of up to 4 weeks)
  • Coping Self-efficacy Scale(Within 2 weeks post-intervention, data were collected over a period of up to 4 weeks)
  • Emotional Avoidance Strategy Inventory For Adolescents(Within 2 weeks post-intervention, data were collected over a period of up to 4 weeks)
  • Perceived Filial Self-Efficacy Scale(Within 2 weeks post-intervention, data were collected over a period of up to 4 weeks)
  • Sibling Cancer Needs Inventory (SCNI)(Within 2 weeks post-intervention, data were collected over a period of up to 4 weeks)
  • Acceptability of Program(Within 2 weeks post-intervention, data were collected over a period of up to 4 weeks)

Study Sites (1)

Loading locations...

Similar Trials