Post Traumatic Stress Disorder Clinical Trial
Official title:
Online PTSD Treatment for Young People and Carers - Case Series
Post Traumatic Stress Disorder (PTSD) is prevalent and impairing in children and young
people. Effective face to face treatments exist, including Cognitive Therapy for PTSD
(CT-PTSD), developed by the researchers' group. However, few young people access effective
treatments.
The researchers are therefore developing a website and smart-phone App that will improve
accessibility of this treatment by allowing trained therapists to deliver CT-PTSD over the
internet (iCT) to young people (12-17 years old) with PTSD. This study aims to provide an
initial evaluation of iCT. This will be done by running an uncontrolled case series with 6
young people.
The objectives of the case series are to: to gauge acceptability of the programme to young
people, carers, and therapists; to measure adherence to the programme; to test the battery of
measures for acceptability; and to obtain estimates of clinical change.
PTSD is prevalent among young people, and is distressing and impairing. Face-to-face
trauma-focussed CBT (TFCBT) is an effective short-term therapy for PTSD in young people. The
researchers previously developed Cognitive Therapy for PTSD (CT-PTSD) in children and young
people, and have shown in 2 published RCTs that it is efficacious when delivered
face-to-face. However, most young people with PTSD do not receive effective, evidence-based
treatments. This is in part due to under-capacity in NHS CAMHS, and in part due to the burden
and inconvenience to young people in attending face-to-face appointments in a clinic. In this
project the researchers propose to make CT for PTSD widely available to young people by
delivering the therapy via the internet, with therapist support. The rationale for this
approach is that (1) young people will engage with internet-delivered therapy, and online
therapies for other disorders such as depression have demonstrated efficacy in clinical
trials; (2) effective online therapies for adults with PTSD have been developed and
evaluated; (3) no online treatments for young people with PTSD have yet been developed.
An uncontrolled case series will be run with N=6 young patients. Young people who are
referred to the South London and Maudsley NHS Foundation Trust CAMHS service, and who meet
the eligibility criteria, will be invited to take part in the case series. After both the
young person and their carer or parent have provided informed consent (or assent), they will
complete several baseline assessment measures. These measures will be completed at a
face-to-face meeting in the Tier 4 National and Specialist Trauma, Anxiety and Depression
(TAD) NHS clinic, and online. The young person and family will meet the young person's
therapist face-to-face at this initial assessment meeting. After assessment, the young person
that will be treated remotely using iCT for up to 12 weeks.
This treatment will include regular (at least weekly) telephone contact with the therapist,
and other contact with the therapist during the week using a messaging function within the
iCT App. The young person will be asked to complete a mood rating and a brief 8-item
questionnaire about PTSD symptoms once a week during treatment: this mirrors what happens
during standard face-to-face care in the TAD NHS clinic. At mid treatment, the young person
will be asked to complete one additional 25-item questionnaire about thoughts related to
trauma. Risk monitoring including monitoring of adverse events will be carried out during
weekly phone calls.
Post treatment, the young person will attend the TAD NHS clinic for a face-to-face clinical
interview and will complete a questionnaire pack online. At this meeting, the young person
will complete feedback ratings on the acceptability of the design of online treatment modules
using 4 simple 0-10 scales (about the overall design appeal, ease-of-use, comprehension, and
likelihood of recommending the program to a friend with similar problems). The young person
will be interviewed about their experience of using the iCT program (an "exit interview").
Acceptability of the questionnaire battery will be assessed by asking young people to
complete an end-of-treatment rating using a 0-100 scale. The young people's parents or carers
will also take part in a clinical interview about the young person, will complete a
questionnaire pack online, and will be invited to take part in an interview about their
experience as a parent or carer of using the iCT program.
N=6 young people will be treated as part of this case series. Young people's and their
parents' qualitative feedback on the acceptability of the iCT programme will be reported
using data from the exit interviews and from the acceptability rating scales. Averse events
during therapy will also be reported. Reliable Clinical Change on a standardised
questionnaire of PTSD symptoms (the CPSS-5) will be reported as a preliminary signal of
clinical effect. Reliable Clinical Improvement is shown by a reduction of 8 points on the
CPSS-5. Acceptability of the outcome measures will be gauged by scrutinising completion
rates.
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