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Clinical Trials/NCT00296907
NCT00296907CompletedNot Applicable

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

University Children's Hospital, Zurich2 sites in 1 country30 target enrollmentStarted: April 1, 2006Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
30
Locations
2
Primary Endpoint
KIDSCREEN: health-related quality of life

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
7 Years to 16 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

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)

Investigators

Sponsor
University Children's Hospital, Zurich
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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