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Psychiatry of Transition in a World in Transition

NCT04333797, Not applicable, Completed, Queen Fabiola Children's University Hospital

Trial 10

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

FieldValueSource
TitlePsychiatry of Transition in a World in TransitionClinicalTrials.gov
NCT numberNCT04333797ClinicalTrials.gov
StatusCompletedClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment252 participants, actualClinicalTrials.gov
Lead sponsorQueen Fabiola Children's University HospitalClinicalTrials.gov
ConditionsTransitional Care, Mental Disorder in Adolescence, Mental HealthClinicalTrials.gov
InterventionsRisk and Protective Factors AssessmentClinicalTrials.gov
First posted2020-04-03ClinicalTrials.gov
Last updated2026-01-07ClinicalTrials.gov

Registered outcomes 20

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescriptionSource
PrimaryChange from Baseline self-rated mental health status (need for care) at 2 yearsChange from Baseline HoNOSCA before transition at 17 y.o. to after transition at 19 y.o.Measured at baseline (T0) and follow-up (T1) with the Health of the Nation Outcome Scale for Children and Adolescents (HoNOSCA).ClinicalTrials.gov
PrimaryChange from Baseline self-rated measure of quality of life at 2 yearsChange from Baseline WHO-QoL before transition at 17 y.o. to after transition at 19 y.oMeasured at baseline (T0) and follow-up (T1) with the Quality of life assessed by World Health Organisation Quality of Life Assessment (WHO-QoL-BREF)ClinicalTrials.gov
SecondarySelf-rated measure of traumatic life eventsBefore transition at 17 y.o. (T0)Measured with Childhood Trauma Questionnaire (CTQ)ClinicalTrials.gov
SecondarySelf-rated measure of family functioningBefore transition at 17 y.o. (T0)Measured with Family Assessment Device (FAD)ClinicalTrials.gov
SecondarySelf-rated measure to quantify the risk of developing psychiatric disordersBefore transition at 17 y.o. (T0)Measured with General Health Questionnaire (GHQ-12)ClinicalTrials.gov
SecondarySelf-rated measure of internalising and externalising symptomsBefore transition at 17 y.o. (T0)Measured with Youth Self Report 11-18 (YSR)ClinicalTrials.gov
SecondarySelf-rated measure of impulsivity and compulsivityBefore transition at 17 y.o. (T0)Measured with Barratt Impulsiveness Scale (BIS-11)ClinicalTrials.gov
SecondarySelf-rated measure of depressivityBefore transition at 17 y.o. (T0)Measured with Beck Depression Inventory-II (BDI-II)ClinicalTrials.gov
SecondarySelf-rated measure of suicidal riskBefore transition at 17 y.o. (T0)Measured with Beck Scale of Suicide Ideation (BSS)ClinicalTrials.gov
SecondarySelf-rated measure of emotional regulationBefore transition at 17 y.o. (T0)Measured with Emotion Regulation Questionnaire for Children and Adolescents (ERQ-CA)ClinicalTrials.gov
SecondarySelf-rated measure of interpersonal relationships social adaptationBefore transition at 17 y.o. (T0)Measured with Social Adaptation Self-evaluation Scale (SASS)ClinicalTrials.gov
SecondarySelf-rated measure of cognitive insightBefore transition at 17 y.o. (T0)Measured with Beck Cognitive Insight Scale (BCIS)ClinicalTrials.gov
SecondaryCognitive assessment - IQBefore transition at 17 y.o. (T0)Measured with Wechsler Adult Intelligence Scale (WAIS-IV)ClinicalTrials.gov
SecondaryExecutive functions assessment - alertness, divided attention, flexibility and working memoryBefore transition at 17 y.o. (T0)Measured with Test of Attentional Performance (TAP)ClinicalTrials.gov
SecondaryExecutive functions assessment - cognitive inhibitionBefore transition at 17 y.o. (T0)Measured with STROOP TaskClinicalTrials.gov
SecondaryExecutive functions assessment - planning taskBefore transition at 17 y.o. (T0)Measured with Tower of London Test (TOL)ClinicalTrials.gov
SecondarySelf-rated measure of executive functionsBefore transition at 17 y.o. (T0)Measured with Behavior Rating Inventory of Executive Function - Self report (BRIEF-SR)ClinicalTrials.gov
SecondarySelf-rated measure of transition readiness and appropriatenessBefore transition at 17 y.o. (T0)Measured with Transition Readiness and Appropriateness Mesure (TRAM)ClinicalTrials.gov
SecondarySelf-rated measure of therapeutic allianceAfter transition at 19 y.o. (T1)Measured with Helping Alliance Questionnaire (HAQ)ClinicalTrials.gov
SecondarySelf-rated measure of transition related outcomesAfter transition at 19 y.o. (T1)Measured with Transition Related Outcomes Mesure (TROM)ClinicalTrials.gov

Outcomes 0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 40

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
2034749BACKGROUNDPubMed
6125971BACKGROUNDPubMed
8312295BACKGROUNDPubMed
8778124BACKGROUNDPubMed
9055514BACKGROUNDPubMed
9169311BACKGROUNDPubMed
10616607BACKGROUNDPubMed
12860775BACKGROUNDPubMed
15085902BACKGROUNDPubMed
15099613BACKGROUNDPubMed
15939837BACKGROUNDPubMed
17249634BACKGROUNDPubMed
17551351BACKGROUNDPubMed
18026842BACKGROUNDPubMed
18573214BACKGROUNDPubMed
19002191BACKGROUNDPubMed
19417667BACKGROUNDPubMed
20884954BACKGROUNDPubMed
21334565BACKGROUNDPubMed
21652063BACKGROUNDPubMed

Grants 0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 2

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource
Stroop Color-Word TestSecondary outcomeConductCognition
Tower PlanningSecondary outcomeConductCognition

Source 5

FieldValueSource
Releasetrials-2026-11-12-0.4.0ClinicalTrials.gov
Release manifest SHA-2560f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov
NIH clinical studies file2026-11-13ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.4.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)