Sustain and Reinforce the Transition From Child to Adult Mental Health Care in Switzerland : A Monocentric Nested Cohort Randomized Controlled Trial: The SORT Study.
- Conditions
- Psychiatric DisorderTransition
- Interventions
- Behavioral: Managed transition
- Registration Number
- NCT04249960
- Lead Sponsor
- University of Geneva, Switzerland
- Brief Summary
Disruption of care during transition from child and adolescent mental health (CAMHS) to adult mental health services (AMHS) may adversely affect the health and well-being of service users. Indeed, transition-related discontinuity of care is a major health and societal challenge today. Current evidences show that this transition is not always properly managed and that improving the transition process can have a positive impact on the health and wellbeing of young people. Nevertheless, data available are still inconsistent and only few studies investigated possible models aimed at improving and operationalize the transition. At present, no information concerning the transition in the Geneva Canton is available.
According to this lack of evidence, the current study aims at: 1) mapping the CAMHS/AMHS interface; 2) evaluating the longitudinal course and outcomes of adolescents approaching the transition boundary (TB) of their CAMHS; 3) determining the effectiveness of an experimental model of managed transition in improving outcomes, compared with usual care; 4) comparing these results with those of the EU funded MILESTONE study from several other European countries.
The investigators will recruit all patients aged ≥ 16 years and 6 months from the Geneva Canton in charge at CAMHS and they will follow them for up to 24 months. CAMHS will be instructed to provide all their service users at the time of transition either usual care or a novel service called "Managed Transition", which will include the use of a new decision support tool, the Transition Readiness and Appropriateness Measure (TRAM). A nested cohort Randomised Controlled Trial (ncRCT) design will be applied to divide patients into the two groups. The health and wellbeing of the young people will be assessed at baseline and then followed-up for 24 months to see whether they transition to AMHS or are discharged or referred to some other service. The investigators will then evaluate what impact the different transition experiences have on young people's health and wellbeing, and whether the process of Managed Transition has any benefits as compared to usual care.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 200
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- provides valid written informed consent, or assent, if below the legal age of consent;
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- age is within 18 months of reaching the transition boundary of their CAMHS - during the trial recruitment period;
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- has a mental disorder defined by DSM-IV-TR, DSM-5 or ICD 10/11, or is under the regular care of CAMHS (if not yet diagnosed);
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- Has an IQ ≥ 70 as ascertained by previous standardized assessment or diagnosed by clinician, or no indication of intellectual impairment.
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- does not provide valid written informed consent, or assent, if below the legal age of consent;
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- is younger than 18 months before the transition boundary of their CAMHS;
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- has intellectual impairment (IQ < 70) as ascertained by standardized assessment or diagnosed by clinician;
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- if not able to (or expected not to be able to) complete the questionnaires due to severe physical disabilities or language problems, even with assistance from family members or research assistant.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Managed transition Managed transition Young people in this group will do the managed transition, they will be our experimental group.
- Primary Outcome Measures
Name Time Method Patient's health status (need for care) Before transition compared to after transition (18 months) Measured at each time point using the Health of the Nation Outcome Scale for Children and Adolescents (HoNOSCA) completed by a trained research assistant. Scores will be compared between first and last time point. HoNOSCA is 5 point scale going from 0 = not a problem, 1 = minor issue not requiring intervention, 2 = slightly problematic, 3 = moderately serious problem, 4 = serious to very serious problem, 9= unknown/not applicable. Scores are calculated by adding up all the subscales (9s are not counted) and a higher score means a worse outcome.
- Secondary Outcome Measures
Name Time Method Client Service Receipt Inventory (CSRI) Baseline, 6, 12 and 18 months Service use assessed by a Client Service Receipt Inventory adapted from the Milestone study; completed by the young person
Barriers to Care (BtC) 6, 12 and 18 months Barriers to care assessed by Barriers to Care checklist completed by the young person if he/she is not using the available services any more
Child Behavior Checklist (CBCL) or Adult Behavior Checklist (ABCL) Baseline and 18 months Emotional and behavioral disturbances measured by the Achenbach System of Empirically Based Assessment (ASEBA) Child Behavior Checklist (CBCL) or Adult Behavior Checklist (ABCL) questionnaires (parent/carer version). CBCL targets young people until 17 and ABCL after 17.
Multidimensional Peer Victimization Scale-Revised (MPVS-R) Baseline and 18 months Multidimensional Peer Victimization Scale-Revised assesses bullying as a self report
Coddington Life Event Scale (CLES) Baseline, 6, 12 and 18 months Important life events is assessed by the Coddington Life Event Scale self-report
Health of the Nation Outcome Scale for Children and Adolescents (HoNOSCA) self report Baseline, 6, 12 and 18 months Self-report "need for care" status measured by the Health of the Nation Outcome Scale for Children and Adolescents
Clinical Global Impression Scale (CGIS) Baseline, 6, 12 and 18 months The Clinical Global Impression Scale completed by the clinician assesses patient's ilness severity
EuroQol generic quality of life questionnaire (5Q-5D-5L) Baseline, 6, 12 and 18 months Quality Adjusted Life Years (QALYs) and cost effectiveness are assessed by EuroQol generic quality of life questionnaire completed by the young person.
On Your Own Feet - Transition Experience Scale (OYOF-TES) 6, 12 or 18 months Transition experience and readiness assessed by On Your Own Feet - Transition Experience Scale completed by the young person and parent/carer only once at the time point right after transition
Health of the Nation Outcome Scale for Children and Adolescents (HoNOSCA) clinician version Baseline, 6, 12, and 18 months Need for care and mental health status measured by Health of the Nation Outcome Scale for Children and Adolescents completed by a trained research assistant with information from the young person, parent/carer and clinician to ensure accuracy
Anticipatory and Consummatory Interpersonal Pleasure Scale (ACIPS) Baseline Social abilities are measured by the Anticipatory and Consummatory Interpersonal Pleasure Scale self report and parent/carer version
Kiddie Schedule for Affective Disorders and Schizophrenia-Present State and Lifetime (K-SADS-PL) Baseline and 18 months Kiddie Schedule for Affective Disorders and Schizophrenia-Present State and Lifetime Version for DSM-IV performed by a trained research assistant
Prodromal questionnaire (PQ-16) Baseline and 18 months Prodromal questionnaire to assess prodromal symptoms filled by the young person as a self report
General Assessment Scale for Social Functioning (GASC) Baseline and 18 months General Assessment Scale for Social Functioning assesses patients general functioning filled by the clinician
Transition Related Outcome Measure (TROM) 6, 12 or 18 months Transition Related Outcome Measure to assess outcomes post-transition completed by the young person, parent/carer and clinician
World Health Organisation's quality of life (WHOQOL-BREF) Baseline and 18 months Young person's quality of life is measured by World Health Organisation's quality of life questionnaire. It is completed by the young person.
Reflective Functioning Questionnaire (RFQ and PRFQ) self-report and parent version Baseline Reflective Functioning Questionnaire assesses mentalisation abilities filled by the young person and parent/carer (two versions)
Perceived Stress Reactivity Scale (PSRS) Baseline Young person's stress status is measured by the Perceived Stress Reactivity Scale self report
Trial Locations
- Locations (1)
University of Geneva
🇨🇭Geneva, Switzerland