F32
Conditions
Interventions
Group 1: Intervention group: Participants receive access to the web-based intervention, comprising 7 modules (45 minutes each, plus an introductory module), daily motivating SMS, weekly homework assig
Sponsors
Abt. für Rehabilitationspsychologie und Psychotherapie, Institut für Psychologie, Albert-Ludwigs-Universität Freiburg
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Depression diagnosis in clinical interview
Exclusion criteria
Exclusion criteria: current psychotherapy, current change of psychopharmaceuticals, exclusion diagnosis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcome is the change of depression severity, measured by the QIDS (Quick Inventory of Depressive Symptomatology, externally assessed during the telephone interview), between baseline (t1) and post-intervention (t2, eight weeks after randomization). In addition, depression severity will be assessed at follow-up (t3, six months after randomization). | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Remission of depression (SCID-1, Structured clinical interview for DSM-V) 2. Depression response (PHQ-9; Patient Health Questionnaire-9) 3. Actitity behavior: Everyday activity (BADS; Behavioral Activation for Depression Scale) 4. Activity behavior: Physical activity (IPAQ-SF; International Physical Activity Questionnaire - Short Form) 5. Motivational and volitional indicators (outcome expectancies, motivational self-efficacy, intention, volitional self-efficacy, action planning, coping planning, action control) 6. Perseverative cognitive processes (RSQ-D; Response Style Questionnaire – German Version) 7. Side effects of the intervention (INEP; Inventar zu Erfassung negativer Effekte von Psychotherapie) All assessments take place at baseline (t1), eight weeks (t2) and six months after randomization (t3). Covid-19-related limitations are recorded at all three time points (self-report). Additionally, sociodemographic information and the initial motivational level will be assessed at baseline (t1; self-report). At t2, received health care services (FIMA) as well as satisfaction with the intervention will be assessed. | — |
Countries
Germany
Contacts
Public ContactClaudia Mueller-Weinitschke
Abt. für Rehabilitationspsychologie und Psychotherapie, Institut für Psychologie, Albert-Ludwigs-Universität Freiburg
Outcome results
None listed