Implementing eHealth Interventions Into Regular Clinical Practice

  • days left to enroll
  • participants needed
  • sponsor
    Oslo University Hospital
Updated on 25 January 2021


The purpose with this study is to test a digital patient-provider communication tool for symptom and needs management among patients with chronic health conditions.


Living with chronic health conditions affects all areas of life. Fatigue, sleeping problems, pain and loneliness are common. In addition to troublesome symptoms that vary in intensity, many experience worry and uncertainty. There is a need to improve the quality of follow-up of patients with chronic health conditions. A digital patient-provider communication tool, which supports shared decision making, can be one way to improve quality.

The digital tool (InvolveMe) will provide patients with the opportunity to complete and submit a symptom and need assessment prior to out-patient visits at the hospital. Also, patients will have the opportunity to use secure e-mail for follow-up from health care providers in between hospital visits. The assessment will allow patient to prioritize what is important to talk with their health care providers about.

Such a tool can help to make changes in symptoms more visible to both patients and health care providers, as well as make it easier to ask for information and guidance to deal with the individual difficulties patients' experience. The goal is to better address symptoms and concerns and to enhance follow up and coordination between consultations as well as increase the quality of life and reduce illness related stress.

The digital communication tool will first be tested in a feasibility pilot study. The tool will be offered to 50 patients (kidney transplant recipients and patients with non-functioning pituitary adenomas). Participants will be given the opportunity to use the digital communication tool with baseline measures and following measures after 3 and 6 months.

After pilot testing of the tool, a larger longitudinal clinical study among 160 patients with non-functioning pituitary adenomas (n=60) and kidney transplant recipients (n=100) will be conducted to assess the clinical utility. The participants will be assigned to use the digital communication tool, and will be followed with repeated measures over 12 months.

Condition Renal Transplant Recipients, Non-functioning Pituitary Adenoma, Non-functioning Pituitary Adenoma, Non-functioning Pituitary Adenoma
Treatment InvolveMe
Clinical Study IdentifierNCT04218721
SponsorOslo University Hospital
Last Modified on25 January 2021


Yes No Not Sure

Inclusion Criteria

Patients with a renal transplant (RTX) OR patients with Non functioning pituitary adenomas (NFPA)
Able to read and speak Norwegian
Have access to a Smart-phone or tablet
Have their own secure access device (BankID)

Exclusion Criteria

Clear my responses

How to participate?

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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