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Clinical Trials/NCT00296907
NCT00296907
Completed
Not Applicable

Psychological Interventions in Siblings of Children With Cancer: a Randomized Controlled Study

University Children's Hospital, Zurich1 site in 1 country30 target enrollmentApril 2006
ConditionsCancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cancer
Sponsor
University Children's Hospital, Zurich
Enrollment
30
Locations
1
Primary Endpoint
KIDSCREEN: health-related quality of life
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

The purpose of the study is to evaluate the effectiveness of a two-session brief psychological intervention in siblings of pediatric cancer patients with regard to behavior problems and depression.

Detailed Description

Within a randomized controlled design the effects of a brief two-session psychological intervention (child, parents) shall be studied in 30 siblings of newly diagnosed pediatric cancer patients. After a baseline assessment 3-4 weeks after diagnosis participants are randomly assigned to an intervention or waiting list group. Both are re-assessed at 3 and 6 months by means of standardized questionnaires assessing psychological adaptation and behavior. The intervention is provided to the waiting list group after the 6-month assessment.

Registry
clinicaltrials.gov
Start Date
April 2006
End Date
December 2010
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Children's Hospital, Zurich
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • brother or sister with newly diagnosed cancer treated at the University Children's Hospital command of the German language normal developmental level

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

KIDSCREEN: health-related quality of life

Time Frame: baseline, 3 and 6 months post intervention

UCLA Child PTSD Reaction Index

Time Frame: baseline, 3 and 6 months post intervention

DIKJ (Depression-Inventory for Children and Adolescents)

Time Frame: baseline, 3 and 6 months post intervention

Spence Children's Anxiety Scale

Time Frame: baseline, 3 and 6 months post intervention

Child Behavior Checklist

Time Frame: Baseline, 3 and 6 months post intervention

Secondary Outcomes

  • Posttraumatic Distress Scale(baseline, 3 and 6 months post intervention)
  • Symptom Checklist 27(baseline, 3 and 6 months post intervention)

Study Sites (1)

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