Data

Personality disorder in young people: Evaluation of Screening measures And the safety and acceptability of relational Peer Work (EScAPe)

Orygen

Dataset description

This dataset captures information from a pilot clinical trial involving young people aged 12-25 years with personality disorder who received up to 10 sessions of relational peer work over 13 weeks. The dataset includes details on treatment attendance, the content of peer work sessions, participant demographics, and outcomes related to psychosocial functioning, distress, self-care, help-seeking behaviors, personality pathology, depressive symptoms, anxiety, and substance use. Additionally, it records fidelity measures, including the use of standardized training resources and supervision for peer workers. The dataset does not include a control group.
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Subjects

FOR: Mental Health |

Source Study

Trial acronym

EScAPe: Evaluation of Screening measures And relational Peer Work

Trial ID

ACTRN12622000962730

Purpose

Treatment

Phase

Not Applicable

Funding

Charities/Societies/Foundations,Perpetual IMPACT Philanthropy Program

Scientific enquiries

Prof Andrew Chanen

Brief Summary

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 ....
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Key Inclusion Criteria

(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.

Key Exclusion Criteria

(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.

Can healthy volunteers participate?

No

 

Population

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

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). ....
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Comparison

Control group Uncontrolled

No control group

Outcomes

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.

Data Dictionary: Not Available

Will individual participant data (IPD) for this trial be available?

yes

What data in particular will be shared?

All of the individual study-related participant data collected during the study, after de-identification.

When will data be available?

Data will be available immediately following publication and for an indefinite time.

Available to whom?

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.

Available for what types of analyses?

To any type of analyses. Assessed on a case-by-case basis.

Source study information is derived from the Australian New Zealand Clinical Trials Registry (ANZCTR). For more information on the ANZCTR, please see anzctr.org.au