Implementing eHealth Interventions Into Regular Clinical Practice

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

23 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-04-24

Study Completion Date

2020-09-28

Brief Summary

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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.

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Detailed Description

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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 is tested in a feasibility pilot study, including 23 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 months.

Conditions

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Renal Transplant Recipients Non-functioning Pituitary Adenoma

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

All participants get access to the ehealth application

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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eHealth application

Participants get access to the eHealth application InvolveMe

Group Type EXPERIMENTAL

InvolveMe

Intervention Type OTHER

An eHealth application that allows participants to report symptoms and needs prior to out-patient visits at the hospital. The application creates a summary that allows patients to prioritize what is important to talk with their health care providers about. Health care providers can use the summary to prepare the consultation.

Interventions

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InvolveMe

An eHealth application that allows participants to report symptoms and needs prior to out-patient visits at the hospital. The application creates a summary that allows patients to prioritize what is important to talk with their health care providers about. Health care providers can use the summary to prepare the consultation.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* 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).