Evaluation of the SignPost Study: a mobile phone messaging intervention to support people bereaved by suicide
Not Applicable
- Conditions
- Suicide bereavementMental Health - Studies of normal psychology, cognitive function and behaviourGriefMental Health - Suicide
- Registration Number
- ACTRN12621001430820
- Lead Sponsor
- niversity of New England
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Stopped early
- Sex
- All
- Target Recruitment
- 105
Inclusion Criteria
To be eligible to take part in this study, participants will need to be:
-18 years or over
-Bereaved by suicide (self-identified) in the last year
-Living in Australia
-Proficient in English language
-Access to a personal mobile phone
-Not currently considering suicide
Exclusion Criteria
None
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome 1: Psychological distress - Clinically significant improvement and deterioration in symptoms assessed via K-10 (Kessler et al., 2003) [Timepoint: baseline (T1), at six-week post-baseline (T2)]
- Secondary Outcome Measures
Name Time Method