AI Article Synopsis

  • - The study tests a new mental health care model called 'highly personalised and measurement-based care' (HP&MBC) for adolescents and young adults with mood disorders, aiming to improve education, employment, and social functioning compared to standard care.
  • - It involves a 24-month trial with 1500 participants aged 15-25 who will be randomly assigned to either HP&MBC or standard care, with social and occupational functioning evaluated after 12 months.
  • - The trial is ethically approved, and results will be shared through various channels while ensuring participant data remains confidential.

Article Abstract

Objectives: Many adolescents and young adults with emerging mood disorders do not achieve substantial improvements in education, employment, or social function after receiving standard youth mental health care. We have developed a new model of care referred to as 'highly personalised and measurement-based care' (HP&MBC). HP&MBC involves repeated assessment of multidimensional domains of morbidity to enable continuous and personalised clinical decision-making. Although measurement-based care is common in medical disease management, it is not a standard practice in mental health. This clinical effectiveness trial tests whether HP&MBC, supported by continuous digital feedback, delivers better functional improvements than standard care and digital support.

Method And Analysis: This controlled implementation trial is a PROBE study (Prospective, Randomised, Open, Blinded End-point) that comprises a multisite 24-month, assessor-blinded, follow-up study of 1500 individuals aged 15-25 years who present for mental health treatment. Eligible participants will be individually randomised (1:1) to 12 months of HP&MBC or standardised clinical care. The primary outcome measure is social and occupational functioning 12 months after trial entry, assessed by the Social and Occupational Functioning Assessment Scale. Clinical and social outcomes for all participants will be monitored for a further 12 months after cessation of active care.

Ethics And Dissemination: This clinical trial has been reviewed and approved by the Human Research Ethics Committee of the Sydney Local Health District (HREC Approval Number: X22-0042 & 2022/ETH00725, Protocol ID: BMC-YMH-003-2018, protocol version: V.3, 03/08/2022). Research findings will be disseminated through peer-reviewed journals, presentations at scientific conferences, and to user and advocacy groups. Participant data will be deidentified.

Trial Registration Number: ACTRN12622000882729.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10583041PMC
http://dx.doi.org/10.1136/bmjopen-2023-072082DOI Listing

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