An open evaluation trial of the ‘LIFE FLeX 4 PTSD’ digital health program for post traumatic stress, anxiety and depressive symptoms.
Not Applicable
- Conditions
- Post-traumatic stressAnxietyDepressionMental Health - AnxietyMental Health - Depression
- Registration Number
- ACTRN12617000576325
- Lead Sponsor
- Federation University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Stopped early
- Sex
- All
- Target Recruitment
- 27
Inclusion Criteria
Participants must be 18 years of age or older. Participants must also endorse having had experienced a traumatic event and report at least a minimal score on the PCL-5 indicating experiencing some recent post-traumatic stress symptoms.
Exclusion Criteria
No internet access, does not create a My Digital Health account (requires the provision of a valid email address), does not provide consent to study conditions.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Post-traumatic stress disorders symptoms using the PCL-5[Pre intervention (Week 0), post intervention (Week 9) and at the 1 month (Week 13) and 3 month (Week 21) follow-up assessment.];Anxiety symptoms using the GAD-7[Pre intervention, during intervention (Week 3, 5, 7), post intervention and at the 1 and 3 month follow-up assessment];Depressive symptoms using the PHQ-9[Pre intervention, during intervention (Week 3, 5, 7), post and at the 1 and 3 month follow-up assessments.]
- Secondary Outcome Measures
Name Time Method