Reducing Cancer Related Fatigue: Untire App as an Evidence-Based mHealth Solutio
Completed
- Conditions
- kanker, kanker-gerelateerde vermoeidheidcancercancer-related fatigue
- Registration Number
- NL-OMON44512
- Lead Sponsor
- niversitair Medisch Centrum Groningen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 750
Inclusion Criteria
- 18 years or older
- has cancer of has had cancer
- has a smartphone
- experiences moderate or severe cancer-related fatigue, as measured with the Fatigue Symptom Inventory with a fatigue composite score of on average 3 or higher
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).
* Do you have a diagnosis of chronic fatigue syndrome (CF)/myalgic encephalomyelitis (ME) or fibromyalgia (FM)?
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The main outcome is the decrease in CRF after twelve weeks of having access to<br /><br>the Untire app compared to controls. </p><br>
- Secondary Outcome Measures
Name Time Method <p>The secondary outcome is improvement in QoL after twelve weeks of having access<br /><br>to the Untire app compared to controls. Information about the usage (% active<br /><br>users versus % non-active users), patterns in use and the parts of the app that<br /><br>are most strongly related to improvements in CRF will be explored using<br /><br>automatically stored user data (log data) in the application. Moderating and<br /><br>mediating factors on CRF and QoL will be assessed using questionnaire and log<br /><br>data. </p><br>