Skip to content

Parents and Young Children under Extreme Stress - PYCES

A pilot randomised clinical trial of trauma-focused cognitive behaviour therapy for posttraumatic stress disorder (PTSD) in young children aged 3-8 years (PYCES)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN35018680
Enrollment
90
Registered
2013-11-18
Start date
2013-07-10
Completion date
Unknown
Last updated
2021-06-28

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

Conditions

Topic: Mental Health Research Network

Interventions

Random allocation to have the treatment straight away (12 weekly sessions) or to wait for 12 weeks. Trauma-Focused CBT, Manualised 12-session developmentally appropriate trauma-focuse
the first half involves the therapist and child only. The second half involves just the therapist and caregiver and provides an opportunity to discuss any problems and the homework. Booster sessions w

Sponsors

Medical Research Council (MRC) (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Exposure to a road traffic accident, an assault, or another discrete traumatic stressor (i.e. any event that involved the threat of death, severe injury, or threat to bodily integrity, or witnessing such an event); 2. Age 3-8 years 3. Target Gender: Male & Female

Exclusion criteria

Exclusion criteria: 1. Intellectual disability 2. Another primary psychiatric diagnosis 3. PTSD following another previous trauma 4. Unconscious for >15 minutes following the traumatic event 5. Not being fluent in English 6. Ongoing exposure to threat 7. History of organic brain damage 8. Risk of self-harm

Design outcomes

Primary

MeasureTime frame
Determine efficacy of TF-CBT as an intervention for young children with PTSD; Timepoint(s): End of study

Secondary

MeasureTime frame
1. Assess feasibility and acceptability of the intervention; timepoint(s): end of study; 2. Assess mediators and moderators of outcome; timepoint(s): end of study 3. Assess the course of PTSD symptoms on young children over the first 3 months post-trauma; timepoint(s): end of prospective study 4. Compare cognitive variables of children with PTSD vs non-PTSD trauma-exposed children; timepoint(s): end of study 5. Investigation of genetic factors in PTSD onset and in treatment response; timepoint(s): end of study 6. Preliminary health economics analysis; timepoint(s): end of study

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 17, 2026