View Clinical Trial (Medical Research Study)
Coping Skills Training (CST) for Children With Chronic Health Conditions - NCT00359775-53201(Clinical Trial 147430)
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Milwaukee |
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State:
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WI |
| Zip Code: |
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53201 |
| Conditions: |
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Rheumatologic Conditions - Epilepsy - Spina Bifida |
| Purpose: |
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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?
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| Study summary: |
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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. |
| Criteria: |
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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:
- Children with cognitive delay |
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| Study is available at: |
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Children's Hospital of Wisconsin
Milwaukee, WI 53201
United States
Primary Contact:
Betsy l. Roth-Wojcicki, MS, CPNP
Email: broth-wojcicki@chw.org
Phone: 414-266-6762 |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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March 21, 2011 |
Modifications to
this listing: |
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