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KIDNET vs Meditation/Relaxation - a Dissemination Randomized Controlled Trial for the Treatment of Traumatized Children After War in Sri Lanka

KIDNET vs Meditation/Relaxation - a Dissemination Randomized Controlled Trial for the Treatment of Traumatized Children After War in Sri Lanka

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00564317
Enrollment
48
Registered
2007-11-27
Start date
2004-09-30
Completion date
2006-01-31
Last updated
2007-11-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post-Traumatic Stress Disorders

Keywords

PTSD, Depression, Suicidality, trauma-focussed treatment, KIDNET, Narrative Exposure Therapy for Children, Meditation, Relaxation, War

Brief summary

The purpose of this study is to assess the efficacy of KIDNET versus a Meditation/Relaxation protocol in treating traumatized children when applied by locally trained teacher counsellors as well as the effectiveness and adequacy of such a treatment in a south-asian war affected stayee child community.

Detailed description

Outcome measures include PTSD symptom score, Depression score, Suicidal ideation and related functioning measures (including school grades)

Interventions

BEHAVIORALKIDNET

Narrative Exposure Therapy for Children - a short term intervention for the treatment of trauma after war, organized violence, torture, abuse and other detrimental life events

BEHAVIORALMeditation/Relaxation

a protocol of traditional/local meditation and relaxation exercises, such as breathing meditation, chanting, body relaxation

Sponsors

NGO vivo e.V.
CollaboratorUNKNOWN
GTZ-German Technical Cooperation, Germany
CollaboratorUNKNOWN
European Refugee Fund
CollaboratorOTHER
German Research Foundation
CollaboratorOTHER
University of Konstanz
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
11 Years to 15 Years
Healthy volunteers
No

Inclusion criteria

* all children with PTSD Diagnosis from six surveyed schools in Vallikamam/Jaffna educational zones age range 11-15

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frame
PTSD-Symptoms according to CAPS-CA (DSM-IV)pre-test, 5-months, 14-months

Secondary

MeasureTime frame
Depression score & Suicidality according to M.I.N.I. KID A and Bpre-test, 5-months, 14-months

Countries

Sri Lanka

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026