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CompletedNCT00296907Updated Jul 30, 2012

Psychological Interventions in Siblings of Children With Cancer

An interventional study of Brief psychological intervention in Cancer, sponsored by University Children's Hospital, Zurich. Completed at 1 site in Switzerland. Open to participants aged 7 Years to 16 Years. Per ClinicalTrials.gov, last updated 2012-07-30.

Sponsored by University Children's Hospital, Zurich · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
7 Years to 16 Years
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Cancer

Keywords

  • cancer
  • siblings
  • behavior
  • psychological adaptation
  • intervention
03

In context

Lead sponsor

University Children's Hospital, Zurich is the lead sponsor of 92 studies on the registry; 23 are open to participants now.

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

04

Who can participate

Ages eligible
7 Years to 16 Years
Sexes eligible
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

Exclusion Criteria:

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
30 participants (actual)

Study arms

  • Experimental
    Psychological Intervention

    2-session psychological intervention

    Behavioral: Brief psychological intervention

Interventions

  • BehavioralBrief psychological intervention

    Psychoeducation, provision of medical knowledge, coping skills training

06

What researchers measure

Primary outcomes

  1. KIDSCREEN: health-related quality of life

    Time frame: baseline, 3 and 6 months post intervention

  2. UCLA Child PTSD Reaction Index

    Time frame: baseline, 3 and 6 months post intervention

  3. DIKJ (Depression-Inventory for Children and Adolescents)

    Time frame: baseline, 3 and 6 months post intervention

  4. Child Behavior Checklist

    Time frame: Baseline, 3 and 6 months post intervention

  5. Spence Children's Anxiety Scale

    Time frame: baseline, 3 and 6 months post intervention

Secondary outcomes

  1. Posttraumatic Distress Scale

    Time frame: baseline, 3 and 6 months post intervention

  2. Symptom Checklist 27

    Time frame: baseline, 3 and 6 months post intervention

07

Study locations

1 site
  • University Children's Hospital Zurich, Psychosomatic and Psychiatry
    Zurich, CH-8032, Switzerland
08

References and documents

Publications

  • Prchal A, Graf A, Bergstraesser E, Landolt MA. A two-session psychological intervention for siblings of pediatric cancer patients: a randomized controlled pilot trial. Child Adolesc Psychiatry Ment Health. 2012 Jan 11;6(1):3. doi: 10.1186/1753-2000-6-3. PubMed 22236392 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 30, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00296907
Lead sponsor
University Children's Hospital, Zurich
Responsible party
Sponsor
First posted
Feb 27, 2006
Start date
Apr 2006
Primary completion
Jul 2010
Completion
Dec 2010
Last update
Jul 30, 2012

Study contacts

Markus A Landolt, PhD
principal investigator · University Children's Hospital Zurich, Psychosomatic and Psychiatry
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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

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