Effects of Internet Support for Cancer Patients on Health Outcomes, Health Care Utilization and Costs: A Randomized Clinical Trial
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Breast Cancer
- Sponsor
- Oslo University Hospital
- Enrollment
- 200
- Locations
- 1
- Primary Endpoint
- Severity and duration of symptom distress
- Status
- Completed
- Last Updated
- 10 years ago
Overview
Brief Summary
Being diagnosed and treated for cancer is usually associated with severe physical symptoms, impaired functional status, complex emotional, psychosocial and existential issues and substantial worries. Failure to help patients with their problems and worries can unnecessarily delay patients' recovery and rehabilitation, lead to chronic functional impairments, anxiety and depression and prolong patients' needs for health care and social services. The objectives of this interdisciplinary, international research project that includes collaboration with HELFO (The Norwegian Health Economy Administration), are to test and compare, in a randomized, controlled trial (RCT), the effects of (1) a practice-integrated online patient-provider communication (OPPC) service including access to asking questions to HELFO, (2) a multi-component Interactive Health Communication Application (IHCA) called WebChoice, and (3) usual care on: patient outcomes, health care and social services use and costs. Breast cancer patients undergoing treatment at three different hospitals in Norway will be randomized into two experimental and one control groups and will be followed with 5 repeated measures over one year. The proposed study will contribute to innovative methods and technologies that can radically improve patient-provider communication, care quality, and continuity of care. The two interventions tested in this study, the OPPC service with and without additional features of WebChoice, represent new forms of interactions and information sharing between patients and clinicians where patients can get seamless access to communication and information services from where and whenever they need it. This could significantly contribute to reducing unnecessary suffering, less fragmented health care, better efficiency, patient safety, patient satisfaction and have an impact on patients' health services utilization. The investigators' work addresses, therefore, important health policy goals with the potential for considerable societal gains.
Investigators
Cornelia Ruland
Professor
Oslo University Hospital
Eligibility Criteria
Inclusion Criteria
- •Patients recently diagnosed with breast cancer and under treatment (radiation, chemotherapy, hormone, or combinations of those)
- •Patients are \> 18 years of age, able to write / read / speak Norwegian and have Internet with secure access (BankID) at home
Exclusion Criteria
- •Excluded are patients who had received radiation on the brain as this may affect their abilities to reliably report their symptoms
Outcomes
Primary Outcomes
Severity and duration of symptom distress
Time Frame: At baseline and at 2, 4, 6, 8 and 12 months
Anxiety and depression
Time Frame: At baseline an at 2, 4, 6, 8 and 12 months
Secondary Outcomes
- Uncertainty in illness(At baseline and at 2, 4, 6, 8 and 12 months)
- Quality of life(At baseline and at 4, 8 and 12 months)
- Self-efficacy(At baseline and at 2, 4, 6, 8 and 12 months)
- Health care costs(Post intervention, at 12 and 18 months)