Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Toronto Metropolitan University
With
Canadian Institutes of Health Research (CIHR)
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Clinician participants (n=120) recruited for this study will either be Operation Stress Injury (OSI) network clinicians, Operational Trauma and Stress Support Centre (OTSSC) network clinicians or community-based clinicians who treat military-related PTSD.
Both male and female clinician participants will be recruited;
Clinician participants will be greater than 18 years.
Mental health clinicians from the clinics and private practitioners will be eligible to participate in the study if they:
1. attend the CPT workshop;
2. are employees of an OSI or OTSSC clinic, are registered VAC clinicians, or are in private practice treating individuals with military-related PTSD;
3. currently provide psychotherapy to military soldiers or veterans with PTSD;
4. consent to be randomized to one of the three study conditions; and,
5. are willing to solicit patient participation.
Eligible patient participants are:
1. client of the clinician participant, who has a diagnosis of PTSD, as determined by clinician independent assessment, and total PCL score equal or greater to 45; and
2. willing to consent to have their sessions audiorecorded and listened to by a fidelity rater and potentially other clinicians teaching and learning CPT. Patients are permitted to continue other psychotherapeutic interventions if not specifically focused on treating PTSD symptoms. Patient participants must be over the age of 18.
You may not be if
1. current uncontrolled psychotic or bipolar disorder;
