CoCo in cancer rehabilitation: evaluation of use, satisfaction and clinical effects
Completed
- Conditions
- cancerichameljike en psychosociale gevolgen na (behandeling van) kankermalignant neoplasm
- Registration Number
- NL-OMON35213
- Lead Sponsor
- Revalidatiecentrum Het Roessingh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 32
Inclusion Criteria
- age > 18 years;
- finished primary curative treatment for > 3 months (except herceptin, Tamoxifen, etc.);
- cancer related symptoms;
- sufficient physical capacities to participate in sport activities twice a week;
- mild to moderate psychosocial symptoms and fatigue (Symptom Checklist-90 < 165; Checklist Individual Strength < 46).
Exclusion Criteria
- palliative demand for care;
- serious psychopathology;
- insufficient understanding of the Dutch language.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The implementation of the CoCo oncology application will be evaluated in terms<br /><br>of use (login, number and type of exercises, fims and questionnaires that have<br /><br>been filled in and/or seen, amount of time that have been spent on the<br /><br>program), satisfaction with the technology (UTAUT questionnaire), satisfaction<br /><br>with the treatment (CSQ) and quality of the provision of the services (SERVQUAL<br /><br>questionnaire). </p><br>
- Secondary Outcome Measures
Name Time Method <p>The clinical effectiveness will be evaluated in terms of burden of the disease<br /><br>(10-point NRS), quality of life (EORTC-QLQ-C30), phyical functioning (SF-36),<br /><br>fatigue (CIS-20), anxiety (HADS-A) and depression (HADS-D).</p><br>