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Randomised Controlled Trial of Cognitive Behaviour Therapy for Journalists to Reduce Posttraumatic Stress Disorder

Randomised Controlled Trial of Therapist-Provided Cognitive Behaviour Therapy for Journalists to Reduce Posttraumatic Stress Disorder

Status
Withdrawn
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12615000332527
Enrollment
120
Registered
2015-04-13
Start date
2016-05-01
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

The rationale of the study is to evaluate the benefits of Cognitive Behaviour Therapy for reducing PTSD in journalists. This study compares the relative effectiveness of (a) Cognitive Behaviour Therapy provided by therapists via telemedicine to journalists compared to the same components which journalists read in manuals provided to them.

Interventions

There are two arms to this trial. Arm 1: Therapist-Administered Cognitive Behaviour Therapy delivered via telemedicine. Arm 2: Self-Administered Cognitive Behaviour Therapy conducted by self-help manual. Therapist-Administered Cognitive Behaviour Therapy is administered once-weekly over 8 weeks on an individual 60 minute basis. Cognitive Behaviour Therapy includes psychoeducation, exposure to trauma memories, and cognitive restructuring of themes related to traumatic experiences. The duration of

There are two arms to this trial. Arm 1: Therapist-Administered Cognitive Behaviour Therapy delivered via telemedicine. Arm 2: Self-Administered Cognitive Behaviour Therapy conducted by self-help manual. Therapist-Administered Cognitive Behaviour Therapy is administered once-weekly over 8 weeks on an individual 60 minute basis. Cognitive Behaviour Therapy includes psychoeducation, exposure to trauma memories, and cognitive restructuring of themes related to traumatic experiences. The duration of the study for any participant will conclude after a 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) (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

Journalists who report diagnostic criteria for posttraumatic stress disorder (as measured on the PTSD Clinician Administered Scale)

Exclusion criteria

(a) inadequate comprehension of English, (b) imminent suicidal intent, (c) psychosis, or (d) concurrent psychotherapy.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026