Reducing Cancer-Related Fatigue: Untire App as an Evidence-Based mHealth Solutio

Completed

Conditions: Cancer related fatigue (Kankergerelateerde vermoeidheid)

Registration Number: NL-OMON20482

Lead Sponsor: niversitair Medisch Centrum GroningenAfd. Gezondheidspsychologie (FA12)Hanzeplein 1POB 30.001 09700 RB Groningen

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Completed

Sex: Not specified

Target Recruitment: 6000

Inclusion Criteria

In order to be eligible to participate in this study, a subject must meet all of the following criteria:

•18 years and older;

Exclusion Criteria

If participants will answer the following statement and question with yes”, they are not perceived eligible to participate:

•I receive treatment for, take medication for or have a diagnosis of a mental disorder (major depression, anxiety disorder, psychotic disorder or addiction).

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Change in cancer related fatigue (CRF) from baseline to 12 weeks, assessed with the self-report questionnaire Fatigue Symptom Inventory (FSI).

Secondary Outcome Measures

Name	Time	Method
- Change in overall quality of life (QoL) from baseline to 12 weeks, assessed with the 1-item on quality of life in the EORTC QLQ-C30 questionnaire. <br /><br>- Insight in usage of the application using log data (automatically stored data about the assessments and activities that users complete). Patterns of usage and most often performed activities will be explored and related to CRF and QoL. <br /><br>- Explore whether domains targeted within the app mediate the relation with users’ outcomes of CRF or QoL. <br /><br>- Moderating factors on CRF and QoL will be explored.<br>