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Clinical Trials/NCT00971009
NCT00971009
Completed
Not Applicable

Effects of Internet Support for Cancer Patients on Health Outcomes, Health Care Utilization and Costs: A Randomized Clinical Trial

Oslo University Hospital1 site in 1 country200 target enrollmentMarch 2010
ConditionsBreast Cancer

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.

Registry
clinicaltrials.gov
Start Date
March 2010
End Date
July 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Oslo University Hospital
Responsible Party
Principal Investigator
Principal Investigator

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)

Study Sites (1)

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