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Cohort Network for Adolescents and Youth With multipLe Mental Health Conditions

NCT07699159, Recruiting, Centre for Addiction and Mental Health

Trial 8

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

FieldValueSource
TitleCohort Network for Adolescents and Youth With multipLe Mental Health ConditionsClinicalTrials.gov
NCT numberNCT07699159ClinicalTrials.gov
StatusRecruitingClinicalTrials.gov
Enrollment1,620 participants, estimatedClinicalTrials.gov
Lead sponsorCentre for Addiction and Mental HealthClinicalTrials.gov
ConditionsMultiple Mental Health Conditions, Child Mental Health, Youth Mental HealthClinicalTrials.gov
First posted2026-07-13ClinicalTrials.gov
Last updated2026-07-13ClinicalTrials.gov

Registered outcomes 96

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

ListOutcomeTime frameDescriptionSource
PrimaryDiagnostic Assessment for the Health SpectrumBaseline and 24 months
The Diagnostic Assessment for the Health Spectrum (DASH) is a semi-structured screener and interview that evaluates a broad range of psychiatric symptoms and associated symptoms. It also assesses a number of physical health symptoms. The DASH is based on the core structure of the Schedule for Affective Disorders and Schizophrenia-SADS and Kiddie-SADS, and includes features of a number of other structured interviews of psychopathology. It provides a diagnostic spectrum in addition to categorical diagnoses that are aligned to the DSM-IV and DSM-5. The completed interview yields a narrative report and summary for clinicians and researchers. There are three versions (adult, child, and parent on child) which take approximately 90-240+ minutes to complete.
ClinicalTrials.gov
PrimaryAdolescent Health HistoryBaseline, 12 months, 24 months
Youth and caregivers will be asked to self-report the presence of health conditions using the Adolescent Health History measure to indicate whether the youth has in the past or currently has any of over 40 common mental or physical health conditions listed. Youth will also be able to add up to four other conditions not listed.
ClinicalTrials.gov
PrimaryAssessment of Quality of LifeBaseline, 3 months, 6 months, 12 months, 18 months, 24 months
The Assessment of Quality of Life (AQoL) measures 5 dimensions: illness, independent living, social relationships, physical senses and psychological well being. Each dimension is measured by three items (a total of 15 items). Total scores can range from a minimum of 20 to a maximum of 99, with higher scores indicating poorer quality of life.
ClinicalTrials.gov
PrimaryBrain-CODE Demographic FormBaseline, 12 months, 24 monthsThe Brain-CODE Demographic Form is a standard form developed by Brain-CODE to capture demographic information from participants.ClinicalTrials.gov
PrimaryBrain-CODE Medical History Form incorporating Developmental History Questionnaire (DHQ) ItemsBaseline, 12 months, 24 monthsThe Brain-CODE Medical History Form is a standard form developed by Brain-CODE to capture medical history in participants.ClinicalTrials.gov
PrimaryCanadian Health Survey on Children and Youth (CHSCY) Childhood Experiences ScaleBaseline, 12 months, 24 months
The Canadian Health Survey on Children and Youth (CHSCY) Childhood Experiences Scale includes 10 items assessing youth's self-reported exposure to different forms of maltreatment by their caregivers, including physical, sexual and emotional abuse, neglect, as well as exposure to violence between caregivers. One additional item captures youth's exposure to corporal punishment. Items have been administered in population-based studies that include samples of youth and adults, as well as clinical observational studies and trials. Total scores can range from a minimum of 10 to a maximum of 50, with higher scores indicating more negative experiences.
ClinicalTrials.gov
PrimaryChild and Youth Resilience MeasureBaseline, 12 months, 24 months, 36 months
The Child and Youth Resilience Measure is a screening tool to explore the resources (individual, relational, communal and cultural) available to individuals that may bolster their resilience. Individuals aged 24+ will be asked to complete the Adult Resilience Measure. This measure includes multiple subscale scores assessing different domains, with scores interpreted separately by subscale.
ClinicalTrials.gov
PrimaryThe Columbia Suicide Severity Rating ScaleBaseline, 24 months
The Columbia Suicide Severity Rating Scale is a validated and widely used rater-administered measure of suicidal ideation and behaviour, and non-suicidal self-injury. It will be administered to all participants. This measure includes multiple subscale scores assessing different domains, with scores interpreted separately by subscale.
ClinicalTrials.gov
PrimarySelf-Injurious Thoughts and Behaviours InterviewBaseline, 24 monthsThe Self-Injurious Thoughts and Behaviours Interview (SITBI) measures self-injurious thoughts and behaviors.ClinicalTrials.gov
PrimaryCanadian Health Survey on Children and Youth (CHSCY) Bullying ScaleBaseline, 12 months, 24 months
The Canadian Health Survey on Children and Youth (CHSCY) Bullying Scale includes 10 items and is designed to assess youth exposure to bullying in the preceding 12 months. Items capture both the type and frequency of bullying, with types of bullying covered by the measure including verbal, physical, relational, and online forms of bullying. Response options are captured on an ordinal scale encompassing: Never, A few Times a Year, Monthly, Weekly, Daily. Total scores can range from a minimum of 10 to a maximum of 50, with higher scores indicating more experiences with bullying.
ClinicalTrials.gov
PrimaryDifficulties in Emotion Regulation Scale Short FormBaseline, 12 months, 24 months, 36 months
The Difficulties in Emotion Regulation Scale Short Form is an 18-item measure used to identify emotional regulation issues. The measure covers 4 dimensions of emotional regulation: awareness and understanding of emotions; acceptance of emotions; the ability to engage in goal-directed behavior and refrain from impulsive behavior when experiencing negative emotions; and access to emotion regulation strategies perceived as effective. Total scores can range from a minimum of 18 to a maximum of 90, with higher scores indicating more difficulties with emotion regulation.
ClinicalTrials.gov
PrimaryEating Disorder Examination Questionnaire (EDE-QS) Short FormBaseline, 3 months, 6 months, 12 months, 18 months, 24 months
The Eating Disorder Examination Questionnaire (EDE-QS) Short Form is a 12-item, self-report questionnaire capturing eating disorder symptoms. Response options are anchored on a 4-point ordinal response scale that captures symptoms over the preceding 7 days. Total scores can range from a minimum of 0 to a maximum of 36, with higher scores indicating the presence of more eating disorder symptoms.
ClinicalTrials.gov
PrimaryGeneral Anxiety Disorder-7Baseline, 3 months, 6 months, 12 months, 18 months, 24 months, 30 months, 36 months, 42 months
The General Anxiety Disorder-7 (GAD-7) measures presence and severity of Generalized Anxiety Disorder. Total scores can range from a minimum of 0 to a maximum of 21, with higher scores indicating greater presence and severity of anxiety symptoms.
ClinicalTrials.gov
PrimaryGeneral Behaviour Inventory-10 ManiaBaseline, 3 months, 6 months, 12 months, 18 months, 24 months, 30 months, 36 months, 42 months
The General Behaviour Inventory-10 Mania measures the presence and severity of mania. Total scores can range from a minimum of 0 to a maximum of 30, with higher scores indicating greater presence and severity of mania.
ClinicalTrials.gov
PrimaryGeneral Life SatisfactionBaseline, 18 months, 30 months
A singular question from the Canadian Social Survey - Quality of Life and Energy Consumption Behaviours measure will be administered to determine life satisfaction. Total scores can range from a minimum of 0 to a maximum of 10, with higher scores indicating greater life satisfaction.
ClinicalTrials.gov
PrimaryThe Goal-Based Outcome (GBO) ToolBaseline, 3 months, 6 months, 12 months, 18 months, 24 months
The Goal-Based Outcome (GBO) Tool aims to measure the progress and outcomes of an intervention in a simple way. It can be applied in any setting and is currently available in 9 languages. The child GBO tool contains a record sheet whereby up to 3 goals with their descriptions can be written down, followed by a goal rating sheet with descriptions and a scale ranging from 0 (Goals not at all met) to 10 (Goal reached). A goal progress chart at the end can be used to rate the progress of the goal across 12 sessions.
ClinicalTrials.gov
PrimaryInternalized Stigma of Mental IllnessBaseline
The Internalized Stigma of Mental Illness (ISMI) scale is a questionnaire measuring self-stigma among persons with psychiatric disorders. This measure includes multiple subscale scores assessing different domains, with scores interpreted separately by subscale.
ClinicalTrials.gov
PrimaryInternational Sedentary Assessment ToolBaseline, 3 months, 6 months, 12 months, 18 months, 24 months
This measure consists of two parts. The first part has six items, and asks questions based on typical weekday activity in the last week. The second part also includes six items and asks questions pertaining to typical weekend activities within the last week. Higher scores equate to more sedentary behaviors in a participant.
ClinicalTrials.gov
PrimaryMcMaster Family Functioning ScaleBaseline, 12 months, 24 months, 36 months
The McMaster Family Functioning Scale is a shorter 12-item assessment developed from The McMaster Family Assessment Device, which is a 60-item questionnaire that measures an individual's perceptions of their family. Total scores can range from a minimum of 12 to a maximum of 48, with higher scores indicating more positive perceptions of family.
ClinicalTrials.gov
PrimaryTreatment LogBaseline, 6 months, 18 months, 24 months, 30 months, 36 months, 42 monthsThis inventory records prescribed treatment and medication, adherence and tolerability every 6 months.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 75

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
678037BACKGROUNDPubMed
2748771BACKGROUNDPubMed
9204677BACKGROUNDPubMed
9255702BACKGROUNDPubMed
9691720BACKGROUNDPubMed
9808931BACKGROUNDPubMed
10472152BACKGROUNDPubMed
10587984BACKGROUNDPubMed
10909877BACKGROUNDPubMed
10937431BACKGROUNDPubMed
10945922BACKGROUNDPubMed
12964174BACKGROUNDPubMed
15183601BACKGROUNDPubMed
15466849BACKGROUNDPubMed
15486169BACKGROUNDPubMed
15719529BACKGROUNDPubMed
16962074BACKGROUNDPubMed
17178616BACKGROUNDPubMed
17329713BACKGROUNDPubMed
17440198BACKGROUNDPubMed

Trial comparisons 0

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

ComparisonSource

Tests 11

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

TestNamed asSource
Delay DiscountingPrimary outcomeConductCognition
Dimensional Change Card SortPrimary outcomeConductCognition
Emotional Stroop TaskPrimary outcomeConductCognition
Eriksen Flanker TaskPrimary outcomeConductCognition
Matrix ReasoningPrimary outcomeConductCognition
Mental RotationPrimary outcomeConductCognition
Pattern and Letter ComparisonPrimary outcomeConductCognition
Picture Order Memory TestPrimary outcomeConductCognition
Size Order Memory TestPrimary outcomeConductCognition
Stroop Color-Word TestPrimary outcomeConductCognition
Verbal LearningPrimary outcomeConductCognition

Source 4

FieldValueSource
Releasetrials-2026-11-12-0.3.0ClinicalTrials.gov
Release manifest SHA-2564a570df2e7274cee2d4fa2959402fab41880e2cd412e4b590390035fbea69391ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.3.0

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.