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  • Mills, KatherineUniversity of Sydney (författare)

A randomised controlled trial of integrated psychological therapy for traumatic stress and substance use among adolescents: Trial protocol

  • Artikel/kapitelEngelska2020

Förlag, utgivningsår, omfång ...

  • 2020-11-30
  • BMJ,2020
  • electronicrdacarrier

Nummerbeteckningar

  • LIBRIS-ID:oai:lup.lub.lu.se:4d06820a-53d5-4ee1-a190-e94ea6656a35
  • https://lup.lub.lu.se/record/4d06820a-53d5-4ee1-a190-e94ea6656a35URI
  • https://doi.org/10.1136/bmjopen-2020-043742DOI

Kompletterande språkuppgifter

  • Språk:engelska
  • Sammanfattning på:engelska

Ingår i deldatabas

Klassifikation

  • Ämneskategori:art swepub-publicationtype
  • Ämneskategori:ref swepub-contenttype

Anmärkningar

  • Introduction: Post-traumatic stress disorder (PTSD) and substance use disorder frequently co-occur and tend to have their onset during adolescence. Although research has highlighted the importance of treating these disorders in an integrated fashion, there is a dearth of empirically validated integrated treatment options for adolescents with this comorbidity. This paper describes the study protocol for a randomised controlled trial (RCT) examining the efficacy of an integrated trauma-focused cognitive–behavioural treatment for traumatic stress and substance use among adolescents (Concurrent Treatment of PTSD and Substance Use Using Prolonged Exposure - Adolescent (COPE-A)), relative to a supportive counselling control condition (Person-Centred Therapy (PCT)). Methods and analysis: A two-arm, parallel, single-blind RCT with blinded follow-up at 4 and 12 months poststudy entry will be conducted in Sydney, Australia. Participants (n~100 adolescents aged 12–18 years) and their caregivers (caregiver participation is optional) will be allocated to undergo either COPE-A or PCT (allocation ratio 1:1) using minimisation. Both therapies will be delivered individually by project psychologists over a maximum of 16 sessions of 60–90 min duration and will include provision of up to four 30 min optional caregiver sessions. The primary outcome will be between-group differences in change in the severity of PTSD symptoms from baseline to 4-month follow-up, as measured by the Clinician-Administered PTSD Scale for Children and Adolescents for DSM-5. Ethics and dissemination: Ethical approval has been obtained from the human research ethics committees of the Sydney Children’s Hospital Network (HREC/17/SCHN/306) and the University of Sydney (HREC 2018/863). Findings will be published in peer-reviewed journals and presented at scientific conferences. Trial registration number: ACTRN12618000785202; Pre-reults.

Ämnesord och genrebeteckningar

Biuppslag (personer, institutioner, konferenser, titlar ...)

  • Barrett, EmmaUniversity of Sydney (författare)
  • Back, SudieMedical University of South Carolina (författare)
  • Cobham, VanessaUniversity of Queensland (författare)
  • Bendall, SarahOrygen - National Centre for Excellence in Youth Mental Health (författare)
  • Perrin, SeanLund University,Lunds universitet,Institutionen för psykologi,Samhällsvetenskapliga institutioner och centrumbildningar,Samhällsvetenskapliga fakulteten,Department of Psychology,Departments of Administrative, Economic and Social Sciences,Faculty of Social Sciences(Swepub:lu)psyc-sep (författare)
  • Brady, KathleenMedical University of South Carolina (författare)
  • Ross, JoanneNational Drug & Alcohol Research Centre,University of New South Wales (författare)
  • Peach, NatalieUniversity of Sydney (författare)
  • Kihas, IvanaUniversity of Sydney (författare)
  • Cassar, JoanneUniversity of Sydney (författare)
  • Schollar-Root, OliviaUniversity of Sydney (författare)
  • Teesson, MareeUniversity of Sydney (författare)
  • University of SydneyMedical University of South Carolina (creator_code:org_t)

Sammanhörande titlar

  • Ingår i:BMJ Open: BMJ102044-6055

Internetlänk

Hitta via bibliotek

  • BMJ Open (Sök värdpublikationen i LIBRIS)

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