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efficacy of an online intervention including a smartphone application for participants with depressive symptoms

efficacy of an online intervention including a smartphone application for participants with depressive symptoms

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00011045
Enrollment
120
Registered
2016-09-01
Start date
2016-09-01
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

Interventions

Group 1: Experimental group: The online self help intervention "AkUt" (an acronym for the german expression "Aktivitätenaufbau und Umdenken trainieren") consists of an online programm that participant

Sponsors

AG Klinische Neuropsychologie, Klinik für Psychiatrie und Psychotherapie Universitätsklinikum Hamburg-Eppendorf
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: informed consent depressive symptoms (PHQ-9>4) access to a PC with internet access access to a smartphone (iphone 5 or newer/Android 4.1 or newer)

Exclusion criteria

Exclusion criteria: no depressive symptoms (PHQ-9<5) acute suicidal tendencies bipolar disorder schizophrenia/psychosis/other disorders from the schizophrenia spectrum neurological illness or dementia

Design outcomes

Primary

MeasureTime frame
The primary outcome is the reduction of depression symptom severity at post assessment (controlled for pre assessment scores), comparing the experimental and control group. For this purpose, participants complete the Patient Health Questionnaire (PHQ-9) at two times of measurement (pre - post, 4 weeks apart).

Secondary

MeasureTime frame
WHO-Quality of Life BREF (WHO-QOL-BREF); Behavioral Activation Depression Scale (BADS); Dysfunctional Attitudes Scale (DAS-18B). Attitudes towards Psychological Online Interventions (APOI). All of the above mentioned questionnares are presented pre and post intervention. only pre intervention: sociodemographics, status of therapy (psychotherapy, medication, etc.) only post: Questionnaire capturing patients satisfaction (ZUF-8) Questionnaire on side effects of the intervention (INEP-on)

Countries

Germany

Contacts

Public ContactThies Lüdtke

AG Klinische Neuropsychologie,Klinik für Psychiatrie und Psychotherapie Universitätsklinikum Hamburg-Eppendorf

t.luedtke@uke.de+49407410 57549

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 6, 2026