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Intelligent, chatbot-assisted ambulatory follow-up care of youth depression

Intelligent, chatbot-assisted ambulatory follow-up care of youth depression - iCAN

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00032966
Enrollment
368
Registered
2024-01-19
Start date
2023-10-12
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

F32 F33 F43.2 F92.0

Interventions

Group 1: iCAN additionally to Care as Usual. iCAN consists of a smartphone app (iCAN app) and psychological telephone support: (1) The iCAN app includes the following elements: (a) a CBT-based, perso
the iCAN app, however, can continue to be used. iCAN usage begins on the day the iCAN app is installed on the smartphone in the clinic. Group 2: Care as Usual

Sponsors

Universität Greifswald
Lead Sponsor

Eligibility

Sex/Gender
All
Age
13 Years to 25 Years

Inclusion criteria

Inclusion criteria: Age: 13;0 to 25;11 years old at the time of study inclusion Primary diagnoses of inpatient treatment: 13;0 to 25;11 years: depressive episodes (F32), recurrent depressive disorders (F33); 13;0 to 17;11 additionally: adjustment disorder–prolonged depressive reaction (F43.21); Disorder of social behavior with depressive disorder (F92.0) Owning a smartphone Insured with a health insurance company that enables its insured persons to participate in the study as part of the selective contract Written consent to participate in the study; for underage patients, additional written consent from at least one person with legal guardianship Sufficient knowledge of the German language

Exclusion criteria

Exclusion criteria: Other primary diagnoses that are at the forefront of inpatient treatment Schizophrenia, schizotypal or delusional disorder (F20-F29) Acute psychosis Acute danger to self or others Linguistic/neurocognitive barriers

Design outcomes

Primary

MeasureTime frame
Reduction in Depressive Symptoms (Children’s Depression Rating Scale – Revised, Montgomery–Åsberg Depression Rating Scale; PHQ-A, PHQ-9)

Secondary

MeasureTime frame
Increased or more timely use of outpatient aftercare services after inpatient therapy (Client Sociodemographic and Service Receipt Inventory) Remission rate (Longitudinal Interval Follow-up Evaluation (LIFE) interview) Psychosocial functioning level (Children's Global Assessment Scale, Global Assessment of Functioning) Quality of life (World Health Organization Quality of Life, single item: “How would you describe your state of health in general?”) Self-efficacy (self-efficacy short scale) Direct and indirect medical costs (Client Sociodemographic and Service Receipt Inventory, routine data from health insurances)

Countries

Germany

Contacts

Public ContactEva-Lotta Brakemeier

Universität Greifswald

eva-lotta.brakemeier@uni-greifswald.de+49 3834 420 3716

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 12, 2026