EScAPe: Evaluation of Screening measures And relational Peer Work
ACTRN12622000962730
Treatment
Not Applicable
Charities/Societies/Foundations,Perpetual IMPACT Philanthropy Program
Prof Andrew Chanen
This pilot clinical trial aims to evaluate the safety and acceptability of relational peer work for young people (aged 12-25 years) with personality disorder. Peer workers are people who have lived experience of mental illness, and are trained to use that experience to provide support for other young people with mental ill health. Participants will be young people attending headspace, who will be offered up to 10 sessions of relational peer work over a 13-week period. In addition to testing safe .... Read more
(i) Aged 12 to 25 years (inclusive); (ii) Score of 9 or more on the 15-item Structured Clinical Interview for DSM-IV Axis II Disorders Personality Questionnaire (SCID-II PQ BPD); (iii) Be a current headspace client; and (iv) Be seeking mental health support.
(i) Currently receiving psychosocial treatment; (ii) Currently receiving peer work; (iii) An acute psychiatric disorder requiring specialist care; (iv) Unable to provide informed consent or comply with study protocol; or (v) Inadequate English fluency to complete study measures.
No
Sample Size 40
Min. age 12 Years
Max. age 25 Years
Sex Both males and females
Condition category Personality disorder
Condition code Mental Health
Intervention code Treatment: Other
Relational peer work Relational peer work is a manualised intervention that aims to provide support and information from the perspective of a peer with lived experience of mental ill-health. Over 13 weeks, participants will be offered up to 10 individual 50-minute relational peer work sessions. These sessions will be delivered weekly, face-to-face (either in person and/or via videoconferencing), and at a location based on participant preference (e.g. at a clinical site and/or in the community). .... Read more
Control group Uncontrolled
No control group
Outcome: Acceptability, assessed as the proportion of young people who consent to participate in the study, determined by data collected by the study team as part of routine study implementation procedures. Timepoint: This will be evaluated at the end of the study.
Outcome: Acceptability, assessed by the proportion of young people who complete the relational peer work intervention, determined by data from the treatment adherence measure.Timepoint: This will be evaluated at the end of the study.
Outcome: Safety, assessed by the proportion of young people withdrawn from the relational peer work, determined by data collected by the study team as part of routine study implementation procedures. Timepoint: This will be evaluated at the end of the study.
yes
All of the individual study-related participant data collected during the study, after de-identification.
Data will be available immediately following publication and for an indefinite time.
Data will potentially be available to researchers from not-for profit organisations, commercial organisations or other based in any location. All data requests will be considered by the data custodian and the primary sponsor on a case-by-case basis. Requests must include a methodologically sound proposal. Specific conditions of use may apply and will be specified in a data sharing agreement (or similar) that the requester must agree to before access is granted. For further information, see Orygen data sharing policy.
To any type of analyses. Assessed on a case-by-case basis.