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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorNemours Children's Clinic

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Participants must be the parent or primary caregiver of a child (ages 0 - 18 years old) diagnosed with cancer.

Participants must be able to speak and read English or Spanish.

Participants must have access to the internet through a computer or mobile device (e.g., smartphone, tablet).

Disqualifiers

PCCC are ineligible to participate if their child is not expected to live longer than six months from the time of potential recruitment

Trial design

Design model

Parallel

Treatments tested in this trial

  • eSCCIP/eSCCIP-SP

    Behavioral

    eSCCIP/eSCCIP-SP is a psychosocial eHealth intervention for PCCC. It consists of four self-guided, web-based modules (including an introductory module) and three telehealth sessions with a study interventionist.

  • Coping Space

    Behavioral

    Coping Space is a psychosocial informational website for PCCC.

Treatment groups

350 Participants
are divided into 2 treatment groups
Group A: eSCCIP/eSCCIP-SPActive comparator 1 intervention
Group B: Coping SpaceActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

K-6

Questionnaire to measure acute distress.

Time frame
Up to 20 weeks

Secondary outcomes

1

Multidimensional Scale of Perceived Social Support

Questionnaire to measure perceived social support from family, friends, and significant other.

Time frame
Up to 20 weeks
2

The COVID-19 Exposure and Family Impact Scale (CEFIS)

The CEFIS assesses the extent to which a family has experienced or been "exposed" to COVID-19 related potentially traumatic events (e.g., economic changes, illness in family) and the impact of these events on the family's functioning and wellbeing.

Time frame
Up to 20 weeks
3

Coping Self-Efficacy Scale

Questionnaire to measure perceived ability to cope effectively with challenging situations across three domains (use problem-focused coping, stop unpleasant emotions and thoughts, get support from friends and family).

Time frame
Up to 20 weeks
4

Cognitive Emotion Regulation Questionnaire

Questionnaire to identify cognitive coping strategies used after a negative event or situation. Measures nine different cognitive coping strategies.

Time frame
Up to 20 weeks

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Nemours Children's Clinic

Lead sponsor

M.D. Anderson Cancer Center

Collaborator

Children's Hospital Los Angeles

Collaborator

University of Virginia

Collaborator