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Evaluation of the effectiveness of a digital aftercare intervention for depression. A prospective randomized controlled trial

Evaluation of the effectiveness of a digital aftercare intervention for depression. A prospective randomized controlled trial - POSITIV

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
DRKS
Registry ID
DRKS00016663
Enrollment
102
Registered
2021-08-18
Start date
2021-10-01
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

F32.1 F32.2 F33.1 F33.2 F32.0 F33.0

Interventions

Group 1: The intervention group is asked to use a gamified smartphone app based on cognitive-behavioral therapy techniques and methods three times per week (approximately 15-20 min each time) for a pe

Sponsors

Friedrich-Alexander-University Erlangen-Nuremberg Department of Clinical Psychology and Psychotherapy
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Access to a smartphone using Android (version 5 or above) or iOS (version 12 or above); moderate or severe depressive episode - including recurrent episodes - (F32.1, F32.2, F.33.1, F33.2); release from inpatient treatment without further treatment within the next four weeks (exluding medical attention and contact to social workers)

Exclusion criteria

Exclusion criteria: Acute suicidality, acute psychotic symptoms, language or neurocognitive barriers, if treatment of following disorders is the priority: addictive disorders, eating disorders, personality disorder

Design outcomes

Primary

MeasureTime frame
Depressive symptoms severity (HAM-D) after 4 and 16 weeks

Secondary

MeasureTime frame
Baseline, Postassessment, Follow-Up: Depressive symptoms severity (PHQ-9), dysfunctional attitudes (DAS), sleep quality (ISI), affective disorders section of the SCID, quality of life (SF-12) intermediate survey: Credibility and Expectancy Questionnaire (CEQ) Baseline: medication Baseline, Follow-up: claiming and costs of medical care, days absent and present at work (TiC-P)

Countries

Germany

Contacts

Public ContactChristian Aljoscha Lukas

Lehrstuhl für Klinische Psychologie und Psychotherapie Friedrich-Alexander-Universität Erlangen-Nürnberg

christian.aljoscha.lukas@fau.de09131-85-67575

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026