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CompletedNCT00359775Updated Feb 20, 2012

Coping Skills Training (CST) for Children With Chronic Health Conditions

A Phase 2 interventional study of Coping Skills Training in Rheumatologic Conditions (JRA,Lupus), Epilepsy and Spina Bifida, sponsored by Children's Hospital and Health System Foundation, Wisconsin. Completed at 1 site in United States. Open to participants aged 8 Years to 12 Years. Per ClinicalTrials.gov, last updated 2012-02-20.

Sponsored by Children's Hospital and Health System Foundation, Wisconsin · Phase 2 and Interventional

Phase
Phase 2
Study type
Interventional
Enrollment
38
Allocation
Randomized
Ages
8 Years to 12 Years
Sex
All
01

Study summary

Purpose of the study The purpose of this study is to pilot an adapted Coping Skills Training (CST) intervention for feasibility and preliminary efficacy with a sample of children 8 to 12 years of age and their parents. The participants in this study at Children's Hospital of Wisconsin are dealing with one of three chronic health conditions (Rheumatologic Conditions, Epilepsy,Spina Bifida, and Asthma).

Research Questions/Study Aims

The research questions addressed in the full study are:

  1. What is the impact of CST on child depression, QOL, health motivation, attitude toward illness, and self-management efficacy?
  2. What is the impact of CST on parent depression, perception of child's quality of life, perception of impact of CHC on family, and family conflict?
Read the detailed description

Many children with chronic health conditions (CHC) are at increased risk for poor adaptation such as psychosocial problems, behavioral disturbances, and decreased quality of life (QOL). Their parents face economic, social and emotional challenges. In addition, management of the CHC and the involvement of the child in that management can severely challenge both child and parent. Effective coping has been shown to moderate the negative impact of CHC. This study is a pilot study to evaluate the feasibility and preliminary efficacy of adapting a Coping Skills Training (CST) intervention developed for children with diabetes. The CST intervention will be adapted for an integrated sample of school-aged children 8 to 12 years of age with four health conditions (Rheumatologic Conditions, Epilepsy,Spina Bifida, and Asthma). The study will be a randomized clinical trial with a wait-list control group. Each arm will consist of 25 families. CST is a 6-session group intervention based on cognitive behavioral and learning theory. The impact of CST on both outcomes (child: depression, QOL; parent: depression, Child QOL, CHC impact on family) and protective factors (child: health motivation, attitude, self-management efficacy; parent: family conflict) will be measured.

02

Conditions studied

  • Rheumatologic Conditions (JRA,Lupus)
  • Epilepsy
  • Spina Bifida
  • Asthma

Keywords

  • Coping
  • psychosocial
  • Quality of Life
  • problem solving
03

In context

Asthma

3,921 studies on the registry are indexed under Asthma; 507 are open to participants now.

This study's enrollment of 38 is below the median of 83 across 2,752 interventional studies indexed under Asthma.

Browse Asthma studies →

Lead sponsor

Children's Hospital and Health System Foundation, Wisconsin is the lead sponsor of 3 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
8 Years to 12 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Male and female children ages 8 to 12 with no known severe cognitive delays,
  • Who are English speaking,
  • With one of the three target conditions; and
  • Have at least one parent willing to participate.

Exclusion criteria

Exclusion Criteria:

  • Children with cognitive delay
05

Study design

Phase
Phase 2
Allocation
Randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
38 participants (actual)

Interventions

  • BehavioralCoping Skills Training

    6 session behavioral program

06

What researchers measure

Primary outcomes

  1. Child Depression measured by Child Depression Inventory (CDI)

    Time frame: ongoing

  2. Parent Depression measured by Beck Depression inventory (BDI)

    Time frame: ongoing

  3. Quality of life measured by Child Health Questionnaire

    Time frame: ongoing

  4. Impact on Family measured by the Impact of Family Scale.

    Time frame: ongoing

07

Study locations

1 site
  • Children's Hospital of Wisconsin
    Milwaukee, Wisconsin 53201, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 20, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00359775
Lead sponsor
Children's Hospital and Health System Foundation, Wisconsin
Collaborators
University of Wisconsin, Madison
Responsible party
Betsy Roth-Wojcicki (Pediatric Nurse Practitioner, Children's Hospital and Health System Foundation, Wisconsin) — Principal investigator
First posted
Aug 2, 2006
Start date
Jul 2006
Primary completion
Jan 2012
Completion
Jan 2012
Last update
Feb 20, 2012

Study contacts

Betsy Roth-Wojcicki, MS, CPNP
principal investigator · Medical College of Wisconsin/Children's Hospital of Wisconsin
Kathleen Sawin, DNS, CPNP,
principal investigator · University of Wisconsin Milwaukee/Children's Hopsital of Wisconsin
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Feb 2012. You cannot join it, but the record below documents what was studied.

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