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Activating primary medical care patients for a depression-preventive lifestyle with individualized e-health interventions (ActiLife)

Activating primary medical care patients for a depression-preventive lifestyle with individualized e-health interventions (ActiLife) - ActiLife

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
DRKS
Registry ID
DRKS00011637
Enrollment
600
Registered
2017-01-25
Start date
2017-01-23
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

subsyndromal depressive symptoms F32 F34.1

Interventions

Group 1: The intervention consists in three computer-generated individually tailored counselling letters and weekly SMS messages over a six month intervention period. The counselling letters and SMS m

Sponsors

Universitätsmedizin Greifswald, Institut für Sozialmedizin und Prävention
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Subsyndromal depressive disorder or mild major depression in the past 12 months (DSM-5-classification, operationalized by PHQ-8: at least 2 DSM-5 criteria fulfilled including at least one core criterion)

Exclusion criteria

Exclusion criteria: Exclusion criteria are severe depression in the past 12 months and depressive symptoms in the past 2 weeks preceding recruitment (phq-8 score >= 20 and symptoms of depressed mood, anhedonia, powerlessness in the past 2 weeks), at risk alcohol consumption (defined by an average daily consumption of >= 12g / >= 24g pure alcohol or at least monthly >= 4 / >= 5 alcoholic drinks at one occasion for women and men, respectively), moderate or severe alcohol use disorder according to DSM-5 (operationalized by AUDIT score >= 20), cognitive impairment, analphabetism or severe disease precluding participation, neither smartphone nor regular e-mail use.

Design outcomes

Secondary

MeasureTime frame
Follow-up assessments will be conducted six and twelve months after study inclusion. The following parameters will be assessed (in case of parameters 2-9 change-scores in relation to baseline values will be analyzed): 1) reappearance of depressive episodes in the follow-up period (Screening items M-CIDI), 2) Change in use of depression preventive strategies (adapted and translated items from Levesque et al. 2011, Am J Health Promot), 4) Change in perceived loneliness (UCLA Loneliness Scale) 5) change in health related quality of life (VR-12) 6) change in well-being (WHO-5) 7) change in positive and negative affect (PANAS) 8) change in psychosocial impairment (role functioning, work impairments and inability; adapted items from M-CIDI Q-section), 9) Changes in health behaviors (physical activity (Godin), fruit and vegetable consumption (WHO-Steps), tobacco smoking), 10) reduction of depression related self-stigmatization (adapted version SSMI-SF).

Primary

MeasureTime frame
Self-reported reduction (twelve months preceeding baseline compared to six month preceeding follow-up) in depressive symptoms (assessed via PHQ-8) in the worst episode.

Countries

Germany

Contacts

Public ContactChristian Meyer

Universitätsmedizin GreifswaldInstitut für Sozialmedizin und Prävention

chmeyer@uni-greifswald.de03834/867723

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 21, 2026