Evaluation of the e-psycho-oncological short-term intervention ‘By your Side’ to reduce cancer-related distress: a pilot study

Evaluation of the e-psycho-oncological short-term intervention ‘By your Side’ to reduce cancer-related distress: a pilot study - By your Side

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00036001

Enrollment

Registered

2025-01-24

Start date

2022-03-04

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

Cancer patients affected by distress

Interventions

Group 1: e-psycho-oncological short-term intervention ‘By your Side’ It aims to support patients in developing psychological resources, managing emotions and coping with stress and anxiety. The inter

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Diagnosis of cancer, good command of the German language and Internet access

Exclusion criteria

Exclusion criteria: None.

Design outcomes

Primary

Measure	Time frame
Distress assessed with the the Perceived Stress Questionnaire (PSQ-20)	—

Secondary

Measure	Time frame
Symptoms of depression (Patient Health Questionnaire-2 (PHQ-2)) and anxiety (The Generalized Anxiety Disorder Scale-2 (GAD-2)), self-efficacy (General Self-Efficacy Scale (GSES)), mindfulness (The Freiburg Mindfulness Inventory (FMI)), usability (System Usability Scale (SUS)), satisfaction (Client Satisfaction Questionnaire adapted to Internet-based Interventions (CSQ-I))	—

Countries

Germany

Contacts

Public ContactAlexander Bäuerle

LVR-Universitätsklinik Essen

alexander.baeuerle@lvr.de+49 201 43 87 55 203

Outcome results

None listed

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