- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02002780
Recognizing and Treating Psychosocial Stress Among Children With Complex Heart Problems
Study Overview
Detailed Description
This research will investigate the psychological stress experienced by children who have had surgery for a complex heart problem. Measures of quality of life among children with heart problems indicate that those 8 to 12 years of age have lower quality of life scores than younger or older children.
Children who survive a critical illness requiring a multi-day stay in a pediatric intensive care unit are at risk for a variety of psychiatric morbidities. Depression, anxiety and post-traumatic stress disorder occur in 7% to 28% of patients.
A systematic review of psychological adjustment among children with heart problems indicates that parent reports (but not child self-reports) are useful in detecting problems with psychological adjustment. While parent reports tend to identify increased social and behaviour problems, child self-reports indicate more frequent symptoms of depression compared to healthy peers.
Study Type
Phase
- Phase 2
Contacts and Locations
Study Locations
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Ontario
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Toronto, Ontario, Canada, M5G 1X8
- The Hospital for Sick Children
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- children who have had surgery for a complex heart problem
- children with heart problems requiring on-going medical care
- age 6 to 12 years
Exclusion Criteria:
- the child has had an intervention (catheterization or surgery) within the previous 6 months,
- the child has an identified cognitive or emotional health disability,
- the child or parents do not speak English sufficiently well to respond to the screening instruments, or
- the child's clinic visit is for an acute illness or change in health status.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Subjects
Children identified during the screening phase of the project as having elevated, but not clinically defined, levels of psychosocial stress will be invited to participate in the intervention phase of this research if they are between 8 and 11 years of age. Screening will identify 6 girls and 6 boys eligible and willing to participate in the intervention phase of the project. |
The intervention will be delivered using a day camp structure, on a weekend or during school break in July 2011.
Separate interventions will be offered for boys and girls.
Each intervention will include two full days (0900 to 1600) of group activities lead by the researchers.
Details of the "camp" activities will be developed by the researchers, based on the types of psychosocial stress identified during the screening phase of the project.
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No Intervention: Control
All families that were screened during the screening phase of this study will complete the final screening instrument assessment, whether or not the child participated in the day camp intervention.
The control group will be comprised of those families that did not participate in the intervention.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Change in psychosocial stress scores resulting from the intervention
Time Frame: Baseline and end of study (at about month 10 -11)
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Baseline and end of study (at about month 10 -11)
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Brian McCrindle, MD, The Hospital for Sick Children, Toronto Canada
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 1000020209
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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