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Randomised Controlled Trial of Cognitive Behavior Therapy and Supportive Counselling for Reduction in Posttraumatic Stress Disorder (PTSD) Symptoms in Acehnese Children

Randomised Controlled Trial of Cognitive Behavior Therapy and Supportive Counselling for Reduction in Posttraumatic Stress Disorder (PTSD) Symptoms in Acehnese Children

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12611000080921
Enrollment
60
Registered
2011-01-21
Start date
2011-03-01
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

This study will randomly allocate children with PTSD to either (a)cognitive behaviour therapy, or (b) supportive counselling. This trial is comparable to a parallel trial being conducted in Acehnese adults (ACTRN12610001085066).

Interventions

This trial is comparable to a parallel trial being conducted in Acehnese adults (ACTRN12610001085066). There are 2 arms to this trial. Arm 1:Cognitive Behaviour Therapy. Arm 2: Supportive Counselling. Therapy is administered in once-weekly 60-minute sessions of one-on-one therapy with a counsellor over 6 weeks. Cognitive Behaviour Therapy includes imaginal reliving of trauma memories, in vivo exposure that includes gradual exposure to feared situations, and cognitive restructuring of the trauma

This trial is comparable to a parallel trial being conducted in Acehnese adults (ACTRN12610001085066). There are 2 arms to this trial. Arm 1:Cognitive Behaviour Therapy. Arm 2: Supportive Counselling. Therapy is administered in once-weekly 60-minute sessions of one-on-one therapy with a counsellor over 6 weeks. Cognitive Behaviour Therapy includes imaginal reliving of trauma memories, in vivo exposure that includes gradual exposure to feared situations, and cognitive restructuring of the trauma experience. The duration of the study for any participant will conclude after the 6-month follow-up assessment, resulting in participation duration of 8 months.

Sponsors

University of New South Wales
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
8 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

(1) Exposure to trauma in Aceh, (2) Meet criteria for PTSD

Exclusion criteria

Suicidal intent, psychotic, substance dependent

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026