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Pragmatic Randomized Control Trial of Telehealth vs Standard Care in Follow-up of Patients With Chronic Conditions (MAO)

Primary Purpose

Chronic Disease, Diabetes, Vascular Diseases

Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Telemedicine: tablet and possibly tools to perform measurements
Sponsored by
University of Oslo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Chronic Disease focused on measuring telemedicine, telehealth, randomized control trial, chronic disease, health services research, primary health care, primary care nursing

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • The patient has a considerable disease burden and comprehensive medical needs
  • The patient has a chronic disease
  • The patient has medium to high risk of worsening of their condition, hospitalization or increased need for health and care services
  • The patient has a high consumption of healthcare services
  • The patient has a reduced level of function
  • The patient is motivated to use telehealth solutions
  • The patient is likely to benefit from the use of telehealth solutions

Exclusion Criteria:

  • The patient is not competent to consent
  • The patient is unable to handle the tablet and the measuring equipment to be used
  • The patient has a substance abuse

Sites / Locations

  • Bodø municipality
  • Eid municipality
  • Ullensaker municipality
  • Kristiansand municipality
  • Larvik municipality
  • Gamle Oslo district, Oslo
  • Grünerløkka district, Oslo
  • Sagene ditrict, Oslo
  • St.Hanshaugen district, Oslo

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

No Intervention

Experimental

Arm Label

Follow-up using telehealth solutions

Standard clinical care

Non-randomized follow-up using telehealth solutions

Arm Description

Participants in this arm are followed up using a telehealth solution, as specified by the National Directorate of Health at the local centre. The actual follow-up is personalized to the individual user. All users receive a tablet, which can be used to answer questions about own health and/or transmit clinical measurements.

Participants in this arm receive standard clinical care in accordance with their medinal needs.

Participants in this arm are followed up using a telehealth solution, as specified by the National Directorate of Health at the local centre. The actual follow-up is personalized to the individual user. All users receive a tablet, which can be used to answer questions about own health and/or transmit clinical measurements. This arm is not randomized, but otherwise identical to the randomized experimental arm.

Outcomes

Primary Outcome Measures

Mean change in health-related quality of life (EuroQol 5 Dimensions 5 Levels (EQ-5D-5L)) from baseline at 6 months
Patient's assessment of her health-related quality of life using the EuroQol 5 Dimensions 5 Levels (EQ-5D-5L) questionnaire. The scale goes from 0 to 1 where higher scores mean a better outcome.
Mean change in health-related quality of life (EuroQol 5 Dimensions 5 Levels (EQ-5D-5L)) from baseline at 12 months
Patient's assessment of her health-related quality of life using the EuroQol 5 Dimensions 5 Levels (EQ-5D-5L) questionnaire. The scale goes from 0 to 1 where higher scores mean a better outcome.
Mean change in health-related quality of life (EuroQol 5 Dimensions 5 Levels (EQ-5D-5L)) from baseline at 18 months
Patient's assessment of her health-related quality of life using the EuroQol 5 Dimensions 5 Levels (EQ-5D-5L) questionnaire. The scale goes from 0 to 1 where higher scores mean a better outcome.
Mean change in health-related quality of life (Visual Analogue Scale (VAS)) from baseline at 6 months
Patient's assessment of her health-related quality of life using Visual Analogue Scale (VAS). The scale goes from 0 to 100 where higher scores mean a better outcome.
Mean change in health-related quality of life (Visual Analogue Scale (VAS)) from baseline at 12 months
Patient's assessment of her health-related quality of life using Visual Analogue Scale (VAS). The scale goes from 0 to 100 where higher scores mean a better outcome.
Mean change in health-related quality of life (Visual Analogue Scale (VAS)) from baseline at 18 months
Patient's assessment of her health-related quality of life using Visual Analogue Scale (VAS). The scale goes from 0 to 100 where higher scores mean a better outcome.
Mean change in overall satisfaction with treatment and follow-up from baseline at 6 months
Patients are asked to assess their overall satisfaction with their health care services: "To what extent are you satisfied with the follow-up of your health?". Answers on a four point scale ranging from "Not satisfied at all" to "Very satisfied"
Mean change in overall satisfaction with treatment and follow-up from baseline at 12 months
Patients are asked to assess their overall satisfaction with their health care services: "To what extent are you satisfied with the follow-up of your health?". Answers on a four point scale ranging from "Not satisfied at all" to "Very satisfied"
Mean change in overall satisfaction with treatment and follow-up from baseline at 18 months
Patients are asked to assess their overall satisfaction with their health care services: "To what extent are you satisfied with the follow-up of your health?". Answers on a four point scale ranging from "Not satisfied at all" to "Very satisfied"
Change in yearly health and care cost per person from baseline at 12 months
The total cost of health and care services per patient is calculated by combining information on the use of health and care services with information about private and public costs of health and care services. Yearly health and care cost per person at baseline is defined as the yearly cost 365 days before inclusion. Similarly, the health and care cost at 12 months in defined as the total cost in the first year after inclusion. The change in mean is the primary outcome measure. Other changes, such as distributional changes, may be of interest.

Secondary Outcome Measures

Mean change in sleep quality from baseline at 6 months
Participants are asked the following question: "If you think about the last 7 days, to what degree have you experienced the following a) had problems sleeping at night b) had problems sleeping too much?" Answers on a four point scale ranging from "Not at all" to "To a very large extent".
Mean change in sleep quality from baseline at 12 months
Participants are asked the following question: "If you think about the last 7 days, to what degree have you experienced the following a) had problems sleeping at night b) had problems sleeping too much?" Answers on a four point scale ranging from "Not at all" to "To a very large extent".
Mean change in sleep quality from baseline at 18 months
Participants are asked the following question: "If you think about the last 7 days, to what degree have you experienced the following a) had problems sleeping at night b) had problems sleeping too much?" Answers on a four point scale ranging from "Not at all" to "To a very large extent".
Mean change in patients' sense of control over their health situation from baseline at 6 months
Participants are asked the following question: "To what extent do you feel that you have control over your health situation?" Answers on a four point scale ranging from "Not at all" to "To a very large extent".
Mean change in patients' sense of control over their health situation from baseline at 12 months
Participants are asked the following question: "To what extent do you feel that you have control over your health situation?" Answers on a four point scale ranging from "Not at all" to "To a very large extent".
Mean change in patients' sense of control over their health situation from baseline at 18 months
Participants are asked the following question: "To what extent do you feel that you have control over your health situation?" Answers on a four point scale ranging from "Not at all" to "To a very large extent".
Mean change in patients' satisfaction with involvement of the GP from baseline at 6 months
Patients answer the question "To what extent do you experience your GP is sufficiently involved in the follow-up of your health?" Answers are reported on a four point scale: "Not at all" to "To a very large extent".
Mean change in patients' satisfaction with involvement of the GP from baseline at 12 months
Patients answer the question "To what extent do you experience your GP is sufficiently involved in the follow-up of your health?" Answers are reported on a four point scale: "Not at all" to "To a very large extent".
Mean change in patients' satisfaction with involvement of the GP from baseline at 18 months
Patients answer the question "To what extent do you experience your GP is sufficiently involved in the follow-up of your health?" Answers are reported on a four point scale: "Not at all" to "To a very large extent".
Mean change in patients' sense of user involvement from baseline at 6 months
Patients are asked "To what extent do you experience that you have opportunity to contribute to your own treatment?" Answers are reported on a four point scale: "Not at all" to "To a very large extent".
Mean change in patients' sense of user involvement from baseline at 12 months
Patients are asked "To what extent do you experience that you have opportunity to contribute to your own treatment?" Answers are reported on a four point scale: "Not at all" to "To a very large extent".
Mean change in patients' sense of user involvement from baseline at 18 months
Patients are asked "To what extent do you experience that you have opportunity to contribute to your own treatment?" Answers are reported on a four point scale: "Not at all" to "To a very large extent".
Mean change in the patients' number of appointments with the GP services from baseline at 12 months
Yearly number of appointments with the GP services at baseline is defined as the yearly use 365 days before inclusion. Similarly, the yearly number of appointments with of the GP services at 12 months is defined as the use in the first year after inclusion. The mean change is the primary outcome measure.
Mean change in the patients' number of outpatient visits from baseline at 12 months
Yearly number of outpatient visits at baseline is defined as the yearly use 365 days before inclusion. Similarly, the yearly number of outpatient visits at 12 months is defined as the use in the first year after inclusion. The mean change is the primary outcome measure.
Mean change in the patients' number of inpatient visits from baseline at 12 months
Yearly number of inpatient visits at baseline is defined as the yearly cost 365 days before inclusion. Similarly, the yearly number of inpatient visits at 12 months is defined as the use in the first year after inclusion. The mean change is the primary outcome measure.
Mean change in the patients' duration of inpatient visits from baseline at 12 months
Total duration of inpatient visits at baseline is defined as the total duration of inpatient visits 365 days before inclusion. Similarly, the total duration of inpatient visits at 12 months is defined as the total duration in the first year after inclusion. The mean change is the primary outcome measure.
Mean change in the patients' number of emergency room visits from baseline at 12 months
Yearly number of emergency room visits at baseline is defined as the yearly use 365 days before inclusion. Similarly, the yearly number of emergency room visits at 12 months is defined as the yearly use in the first year after inclusion. The mean change is the primary outcome measure.
Mean change in the patients' number of home nursing visits from baseline at 6 months
Use of home nursing visits before inclusion is measured as the total number of home nursing visits 30 to 60 days prior to inclusion. Use at 6 months is measured as the total number of home nursing visits 150 to 180 days after inclusion.
Mean change in the patients' number of home nursing visits from baseline at 12 months
Use of home nursing visits before inclusion is measured as the total number of home nursing visits 30 to 60 days prior to inclusion. Use at 12 months is measured as the total number of home nursing visits 335 to 365 days after inclusion.
Mean change in the patients' number of home nursing visits from baseline at 18 months
Use of home nursing visits before inclusion is measured as the total number of home nursing visits 30 to 60 days prior to inclusion. Use at 18 months is measured as the total number of home nursing visits 515 to 545 days after inclusion.
Mean change in the patients' duration of home nursing visits from baseline at 6 months
Total duration of home nursing visits before inclusion is measured as the total duration of home nursing visits 30 to 60 days prior to inclusion. Total duration at 6 months is measured as the total duration of home nursing visits 150 to 180 days after inclusion.
Mean change in the patients' duration of home nursing visits from baseline at 12 months
Total duration of home nursing visits before inclusion is measured as the total duration of home nursing visits 30 to 60 days prior to inclusion. Total duration at 12 months is measured as the total duration of home nursing visits 335 to 365 days after inclusion.
Mean change in the patients' duration of home nursing visits from baseline at 18 months
Total duration of home nursing visits before inclusion is measured as the total duration of home nursing visits 30 to 60 days prior to inclusion. Total duration at 18 months is measured as the total duration of home nursing visits 515 to 545 days after inclusion.
Mean change in the patients' number of municipal emergency day care unit visits from baseline at 6 months
Use of municipal emergency day care unit visits before inclusion is measured as the total number of municipal emergency day care unit visits 30 to 60 days prior to inclusion. Use at 6 months is measured as the total number of municipal emergency day care unit visits 150 to 180 days after inclusion.
Mean change in the patients' number of municipal emergency day care unit visits from baseline at 12 months
Use of municipal emergency day care unit visits before inclusion is measured as the total number of municipal emergency day care unit visits 30 to 60 days prior to inclusion. Use at 12 months is measured as the total number of municipal emergency day care unit visits 335 to 365 days after inclusion.
Mean change in the patients' number of municipal emergency day care unit visits from baseline at 18 months
Use of municipal emergency day care unit visits before inclusion is measured as the total number of municipal emergency day care unit visits 30 to 60 days prior to inclusion. Use at 18 months is measured as the total number of municipal emergency day care unit visits 515 to 545 days after inclusion.
Mean change in the patients' duration of municipal emergency day care unit visits from baseline at 6 months
Total duration of municipal emergency day care unit visits before inclusion is measured as the total duration of municipal emergency day care unit visits 30 to 60 days prior to inclusion. Total duration at 6 months is measured as the total duration of municipal emergency day care unit visits 150 to 180 days after inclusion.
Mean change in the patients' duration of municipal emergency day care unit visits from baseline at 12 months
Total duration of municipal emergency day care unit visits before inclusion is measured as the total duration of municipal emergency day care unit visits 30 to 60 days prior to inclusion. Total duration at 12 months is measured as the total duration of municipal emergency day care unit visits 335 to 365 days after inclusion.
Mean change in the patients' duration of municipal emergency day care unit visits from baseline at 18 months
Total duration of municipal emergency day care unit visits before inclusion is measured as the total duration of municipal emergency day care unit visits 30 to 60 days prior to inclusion. Total duration at 18 months is measured as the total duration of municipal emergency day care unit visits 515 to 545 days after inclusion.

Full Information

First Posted
July 5, 2019
Last Updated
October 6, 2021
Sponsor
University of Oslo
Collaborators
Oslo Economics, Norwegian Centre for Rural Medicine, Norsk Gallup Institutt AS
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1. Study Identification

Unique Protocol Identification Number
NCT04142710
Brief Title
Pragmatic Randomized Control Trial of Telehealth vs Standard Care in Follow-up of Patients With Chronic Conditions
Acronym
MAO
Official Title
A Pragmatic Randomized Control Trial Comparing Telehealth With Standard Clinical Care in the Follow-up of Patients With Chronic Conditions Within the Primary Care Setting
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
February 9, 2019 (Actual)
Primary Completion Date
June 30, 2021 (Actual)
Study Completion Date
June 30, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Oslo
Collaborators
Oslo Economics, Norwegian Centre for Rural Medicine, Norsk Gallup Institutt AS

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The Norwegian health authorities has initiated a three-year trial of telehealth solutions as part of the treatment of patients with chronic illness in the period 2018-2021. Within the trial, telehealth indicates that patients are followed-up outside health-care facilities using information and communication technologies (ICTs). Patients who are followed up using telehealth solutions can answer questions about their own health and/or perform measurements related to their health (e.g. blood pressure, blood glucose, oxygen measurement, weight) via a tablet according to a personalized schedule. The measurement values are transferred from the measuring devices to a tablet so that the users can easily see them and track their results over time. The results are also transmitted digitally to a follow-up service, a healthcare center with nurses, who contacts the patient when needed. The follow-up service provides medical support and guidance based on the patient's needs and planned follow-up, and will, in consultation with the user, evaluate whether the user should contact the general practitioner (GP) or emergency room. The study population of the trial includes users with comprehensive medical needs, with medium to high risk of worsening of their condition, hospitalization or increased need for health and care services. The evaluation includes three main parts: 1) An effect evaluation which is designed as a randomized control trial, 2) a cost-benefit analysis, and 3) a process evaluation which aims to provide recommendations for how to organize and implement telemedicine in clinical practice. The primary outcomes include physical and mental health state, patient experience and use of health services. The effect evaluation is designed as a pragmatic open label multi-center randomized control trial, with two parallel arms with 300 patients in each arm. Patients are recruited between February 2019 and June 2020.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Disease, Diabetes, Vascular Diseases, Chronic Lung Disease, Cancer, Psychiatric Disorder
Keywords
telemedicine, telehealth, randomized control trial, chronic disease, health services research, primary health care, primary care nursing

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
732 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Follow-up using telehealth solutions
Arm Type
Experimental
Arm Description
Participants in this arm are followed up using a telehealth solution, as specified by the National Directorate of Health at the local centre. The actual follow-up is personalized to the individual user. All users receive a tablet, which can be used to answer questions about own health and/or transmit clinical measurements.
Arm Title
Standard clinical care
Arm Type
No Intervention
Arm Description
Participants in this arm receive standard clinical care in accordance with their medinal needs.
Arm Title
Non-randomized follow-up using telehealth solutions
Arm Type
Experimental
Arm Description
Participants in this arm are followed up using a telehealth solution, as specified by the National Directorate of Health at the local centre. The actual follow-up is personalized to the individual user. All users receive a tablet, which can be used to answer questions about own health and/or transmit clinical measurements. This arm is not randomized, but otherwise identical to the randomized experimental arm.
Intervention Type
Device
Intervention Name(s)
Telemedicine: tablet and possibly tools to perform measurements
Intervention Description
Users of telemedicine can answer simple questions about their health condition and/or perform measurements related to their health (e.g., blood pressure, blood sugar, oxygen saturation, weight) via a tablet or a similar device. The results are transferred from the measuring devices to the tablet so that users can easily see them and track their own results over time. The results are transmitted digitally to a follow-up service. The follow-up service contacts the patient in case of signs of deterioration or when measurements lie outside what is normal values for the individual. The follow-up service provides medical support and guidance based on the patient's needs and plan for follow-up, and will, in consultation with the patient, assess whether this should contact their GP/emergency room.
Primary Outcome Measure Information:
Title
Mean change in health-related quality of life (EuroQol 5 Dimensions 5 Levels (EQ-5D-5L)) from baseline at 6 months
Description
Patient's assessment of her health-related quality of life using the EuroQol 5 Dimensions 5 Levels (EQ-5D-5L) questionnaire. The scale goes from 0 to 1 where higher scores mean a better outcome.
Time Frame
Measured as change from baseline to 6 months after inclusion
Title
Mean change in health-related quality of life (EuroQol 5 Dimensions 5 Levels (EQ-5D-5L)) from baseline at 12 months
Description
Patient's assessment of her health-related quality of life using the EuroQol 5 Dimensions 5 Levels (EQ-5D-5L) questionnaire. The scale goes from 0 to 1 where higher scores mean a better outcome.
Time Frame
Measured as change from baseline to 12 months after inclusion
Title
Mean change in health-related quality of life (EuroQol 5 Dimensions 5 Levels (EQ-5D-5L)) from baseline at 18 months
Description
Patient's assessment of her health-related quality of life using the EuroQol 5 Dimensions 5 Levels (EQ-5D-5L) questionnaire. The scale goes from 0 to 1 where higher scores mean a better outcome.
Time Frame
Measured as change from baseline to 18 months after inclusion
Title
Mean change in health-related quality of life (Visual Analogue Scale (VAS)) from baseline at 6 months
Description
Patient's assessment of her health-related quality of life using Visual Analogue Scale (VAS). The scale goes from 0 to 100 where higher scores mean a better outcome.
Time Frame
Measured as change from baseline to 6 months after inclusion
Title
Mean change in health-related quality of life (Visual Analogue Scale (VAS)) from baseline at 12 months
Description
Patient's assessment of her health-related quality of life using Visual Analogue Scale (VAS). The scale goes from 0 to 100 where higher scores mean a better outcome.
Time Frame
Measured as change from baseline to 12 months after inclusion
Title
Mean change in health-related quality of life (Visual Analogue Scale (VAS)) from baseline at 18 months
Description
Patient's assessment of her health-related quality of life using Visual Analogue Scale (VAS). The scale goes from 0 to 100 where higher scores mean a better outcome.
Time Frame
Measured as change from baseline to 18 months after inclusion
Title
Mean change in overall satisfaction with treatment and follow-up from baseline at 6 months
Description
Patients are asked to assess their overall satisfaction with their health care services: "To what extent are you satisfied with the follow-up of your health?". Answers on a four point scale ranging from "Not satisfied at all" to "Very satisfied"
Time Frame
Measured as change from baseline to 6 months after inclusion
Title
Mean change in overall satisfaction with treatment and follow-up from baseline at 12 months
Description
Patients are asked to assess their overall satisfaction with their health care services: "To what extent are you satisfied with the follow-up of your health?". Answers on a four point scale ranging from "Not satisfied at all" to "Very satisfied"
Time Frame
Measured as change from baseline to 12 months after inclusion
Title
Mean change in overall satisfaction with treatment and follow-up from baseline at 18 months
Description
Patients are asked to assess their overall satisfaction with their health care services: "To what extent are you satisfied with the follow-up of your health?". Answers on a four point scale ranging from "Not satisfied at all" to "Very satisfied"
Time Frame
Measured as change from baseline to 18 months after inclusion
Title
Change in yearly health and care cost per person from baseline at 12 months
Description
The total cost of health and care services per patient is calculated by combining information on the use of health and care services with information about private and public costs of health and care services. Yearly health and care cost per person at baseline is defined as the yearly cost 365 days before inclusion. Similarly, the health and care cost at 12 months in defined as the total cost in the first year after inclusion. The change in mean is the primary outcome measure. Other changes, such as distributional changes, may be of interest.
Time Frame
Yearly health and care cost per person is calculated at baseline and at 12 months after inclusion.
Secondary Outcome Measure Information:
Title
Mean change in sleep quality from baseline at 6 months
Description
Participants are asked the following question: "If you think about the last 7 days, to what degree have you experienced the following a) had problems sleeping at night b) had problems sleeping too much?" Answers on a four point scale ranging from "Not at all" to "To a very large extent".
Time Frame
Measured as change from baseline to 6 months after inclusion
Title
Mean change in sleep quality from baseline at 12 months
Description
Participants are asked the following question: "If you think about the last 7 days, to what degree have you experienced the following a) had problems sleeping at night b) had problems sleeping too much?" Answers on a four point scale ranging from "Not at all" to "To a very large extent".
Time Frame
Measured as change from baseline to 12 months after inclusion
Title
Mean change in sleep quality from baseline at 18 months
Description
Participants are asked the following question: "If you think about the last 7 days, to what degree have you experienced the following a) had problems sleeping at night b) had problems sleeping too much?" Answers on a four point scale ranging from "Not at all" to "To a very large extent".
Time Frame
Measured as change from baseline to 18 months after inclusion
Title
Mean change in patients' sense of control over their health situation from baseline at 6 months
Description
Participants are asked the following question: "To what extent do you feel that you have control over your health situation?" Answers on a four point scale ranging from "Not at all" to "To a very large extent".
Time Frame
Measured as change from baseline to 6 months after inclusion
Title
Mean change in patients' sense of control over their health situation from baseline at 12 months
Description
Participants are asked the following question: "To what extent do you feel that you have control over your health situation?" Answers on a four point scale ranging from "Not at all" to "To a very large extent".
Time Frame
Measured as change from baseline to 12 months after inclusion
Title
Mean change in patients' sense of control over their health situation from baseline at 18 months
Description
Participants are asked the following question: "To what extent do you feel that you have control over your health situation?" Answers on a four point scale ranging from "Not at all" to "To a very large extent".
Time Frame
Measured as change from baseline to 18 months after inclusion
Title
Mean change in patients' satisfaction with involvement of the GP from baseline at 6 months
Description
Patients answer the question "To what extent do you experience your GP is sufficiently involved in the follow-up of your health?" Answers are reported on a four point scale: "Not at all" to "To a very large extent".
Time Frame
Measured as change from baseline to 6 months after inclusion
Title
Mean change in patients' satisfaction with involvement of the GP from baseline at 12 months
Description
Patients answer the question "To what extent do you experience your GP is sufficiently involved in the follow-up of your health?" Answers are reported on a four point scale: "Not at all" to "To a very large extent".
Time Frame
Measured as change from baseline to 12 months after inclusion
Title
Mean change in patients' satisfaction with involvement of the GP from baseline at 18 months
Description
Patients answer the question "To what extent do you experience your GP is sufficiently involved in the follow-up of your health?" Answers are reported on a four point scale: "Not at all" to "To a very large extent".
Time Frame
Measured as change from baseline to 18 months after inclusion
Title
Mean change in patients' sense of user involvement from baseline at 6 months
Description
Patients are asked "To what extent do you experience that you have opportunity to contribute to your own treatment?" Answers are reported on a four point scale: "Not at all" to "To a very large extent".
Time Frame
Measured as change from baseline to 6 months after inclusion
Title
Mean change in patients' sense of user involvement from baseline at 12 months
Description
Patients are asked "To what extent do you experience that you have opportunity to contribute to your own treatment?" Answers are reported on a four point scale: "Not at all" to "To a very large extent".
Time Frame
Measured as change from baseline to 12 months after inclusion
Title
Mean change in patients' sense of user involvement from baseline at 18 months
Description
Patients are asked "To what extent do you experience that you have opportunity to contribute to your own treatment?" Answers are reported on a four point scale: "Not at all" to "To a very large extent".
Time Frame
Measured as change from baseline to 18 months after inclusion
Title
Mean change in the patients' number of appointments with the GP services from baseline at 12 months
Description
Yearly number of appointments with the GP services at baseline is defined as the yearly use 365 days before inclusion. Similarly, the yearly number of appointments with of the GP services at 12 months is defined as the use in the first year after inclusion. The mean change is the primary outcome measure.
Time Frame
Yearly use of the GP services is calculated at baseline and at 12 months after inclusion.
Title
Mean change in the patients' number of outpatient visits from baseline at 12 months
Description
Yearly number of outpatient visits at baseline is defined as the yearly use 365 days before inclusion. Similarly, the yearly number of outpatient visits at 12 months is defined as the use in the first year after inclusion. The mean change is the primary outcome measure.
Time Frame
Yearly number of outpatient visits is calculated at baseline and at 12 months after inclusion.
Title
Mean change in the patients' number of inpatient visits from baseline at 12 months
Description
Yearly number of inpatient visits at baseline is defined as the yearly cost 365 days before inclusion. Similarly, the yearly number of inpatient visits at 12 months is defined as the use in the first year after inclusion. The mean change is the primary outcome measure.
Time Frame
Yearly number of inpatient visits is calculated at baseline and at 12 months after inclusion.
Title
Mean change in the patients' duration of inpatient visits from baseline at 12 months
Description
Total duration of inpatient visits at baseline is defined as the total duration of inpatient visits 365 days before inclusion. Similarly, the total duration of inpatient visits at 12 months is defined as the total duration in the first year after inclusion. The mean change is the primary outcome measure.
Time Frame
Total duration of inpatient visits is calculated at baseline and at 12 months after inclusion.
Title
Mean change in the patients' number of emergency room visits from baseline at 12 months
Description
Yearly number of emergency room visits at baseline is defined as the yearly use 365 days before inclusion. Similarly, the yearly number of emergency room visits at 12 months is defined as the yearly use in the first year after inclusion. The mean change is the primary outcome measure.
Time Frame
Yearly number of emergency room visits is calculated at baseline and at 12 months after inclusion.
Title
Mean change in the patients' number of home nursing visits from baseline at 6 months
Description
Use of home nursing visits before inclusion is measured as the total number of home nursing visits 30 to 60 days prior to inclusion. Use at 6 months is measured as the total number of home nursing visits 150 to 180 days after inclusion.
Time Frame
Use of home nursing visits is measured one month prior to inclusion and 6 months after inclusion.
Title
Mean change in the patients' number of home nursing visits from baseline at 12 months
Description
Use of home nursing visits before inclusion is measured as the total number of home nursing visits 30 to 60 days prior to inclusion. Use at 12 months is measured as the total number of home nursing visits 335 to 365 days after inclusion.
Time Frame
Use of home nursing visits is measured one month prior to inclusion and 12 months after inclusion.
Title
Mean change in the patients' number of home nursing visits from baseline at 18 months
Description
Use of home nursing visits before inclusion is measured as the total number of home nursing visits 30 to 60 days prior to inclusion. Use at 18 months is measured as the total number of home nursing visits 515 to 545 days after inclusion.
Time Frame
Use of home nursing visits is measured one month prior to inclusion and 18 months after inclusion.
Title
Mean change in the patients' duration of home nursing visits from baseline at 6 months
Description
Total duration of home nursing visits before inclusion is measured as the total duration of home nursing visits 30 to 60 days prior to inclusion. Total duration at 6 months is measured as the total duration of home nursing visits 150 to 180 days after inclusion.
Time Frame
Total duration of home nursing visits is measured one month prior to inclusion and 6 months after inclusion.
Title
Mean change in the patients' duration of home nursing visits from baseline at 12 months
Description
Total duration of home nursing visits before inclusion is measured as the total duration of home nursing visits 30 to 60 days prior to inclusion. Total duration at 12 months is measured as the total duration of home nursing visits 335 to 365 days after inclusion.
Time Frame
Total duration of home nursing visits is measured one month prior to inclusion and 12 months after inclusion.
Title
Mean change in the patients' duration of home nursing visits from baseline at 18 months
Description
Total duration of home nursing visits before inclusion is measured as the total duration of home nursing visits 30 to 60 days prior to inclusion. Total duration at 18 months is measured as the total duration of home nursing visits 515 to 545 days after inclusion.
Time Frame
Total duration of home nursing visits is measured one month prior to inclusion and 18 months after inclusion.
Title
Mean change in the patients' number of municipal emergency day care unit visits from baseline at 6 months
Description
Use of municipal emergency day care unit visits before inclusion is measured as the total number of municipal emergency day care unit visits 30 to 60 days prior to inclusion. Use at 6 months is measured as the total number of municipal emergency day care unit visits 150 to 180 days after inclusion.
Time Frame
Use of municipal emergency day care unit visits is measured one month prior to inclusion and 6 months after inclusion.
Title
Mean change in the patients' number of municipal emergency day care unit visits from baseline at 12 months
Description
Use of municipal emergency day care unit visits before inclusion is measured as the total number of municipal emergency day care unit visits 30 to 60 days prior to inclusion. Use at 12 months is measured as the total number of municipal emergency day care unit visits 335 to 365 days after inclusion.
Time Frame
Use of municipal emergency day care unit visits is measured one month prior to inclusion and 12 months after inclusion.
Title
Mean change in the patients' number of municipal emergency day care unit visits from baseline at 18 months
Description
Use of municipal emergency day care unit visits before inclusion is measured as the total number of municipal emergency day care unit visits 30 to 60 days prior to inclusion. Use at 18 months is measured as the total number of municipal emergency day care unit visits 515 to 545 days after inclusion.
Time Frame
Use of municipal emergency day care unit visits is measured one month prior to inclusion and 18 months after inclusion.
Title
Mean change in the patients' duration of municipal emergency day care unit visits from baseline at 6 months
Description
Total duration of municipal emergency day care unit visits before inclusion is measured as the total duration of municipal emergency day care unit visits 30 to 60 days prior to inclusion. Total duration at 6 months is measured as the total duration of municipal emergency day care unit visits 150 to 180 days after inclusion.
Time Frame
Total duration of municipal emergency day care unit visits is measured one month prior to inclusion and 6 months after inclusion.
Title
Mean change in the patients' duration of municipal emergency day care unit visits from baseline at 12 months
Description
Total duration of municipal emergency day care unit visits before inclusion is measured as the total duration of municipal emergency day care unit visits 30 to 60 days prior to inclusion. Total duration at 12 months is measured as the total duration of municipal emergency day care unit visits 335 to 365 days after inclusion.
Time Frame
Total duration of municipal emergency day care unit visits is measured one month prior to inclusion and 12 months after inclusion.
Title
Mean change in the patients' duration of municipal emergency day care unit visits from baseline at 18 months
Description
Total duration of municipal emergency day care unit visits before inclusion is measured as the total duration of municipal emergency day care unit visits 30 to 60 days prior to inclusion. Total duration at 18 months is measured as the total duration of municipal emergency day care unit visits 515 to 545 days after inclusion.
Time Frame
Total duration of municipal emergency day care unit visits is measured one month prior to inclusion and 18 months after inclusion.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The patient has a considerable disease burden and comprehensive medical needs The patient has a chronic disease The patient has medium to high risk of worsening of their condition, hospitalization or increased need for health and care services The patient has a high consumption of healthcare services The patient has a reduced level of function The patient is motivated to use telehealth solutions The patient is likely to benefit from the use of telehealth solutions Exclusion Criteria: The patient is not competent to consent The patient is unable to handle the tablet and the measuring equipment to be used The patient has a substance abuse
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tor Iversen, Professor
Organizational Affiliation
University of Oslo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Bodø municipality
City
Bodø
Country
Norway
Facility Name
Eid municipality
City
Eidfjord
Country
Norway
Facility Name
Ullensaker municipality
City
Jessheim
Country
Norway
Facility Name
Kristiansand municipality
City
Kristiansand
Country
Norway
Facility Name
Larvik municipality
City
Larvik
Country
Norway
Facility Name
Gamle Oslo district, Oslo
City
Oslo
Country
Norway
Facility Name
Grünerløkka district, Oslo
City
Oslo
Country
Norway
Facility Name
Sagene ditrict, Oslo
City
Oslo
Country
Norway
Facility Name
St.Hanshaugen district, Oslo
City
Oslo
Country
Norway

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Researchers are not allowed to share individual patient data with other researchers.

Learn more about this trial

Pragmatic Randomized Control Trial of Telehealth vs Standard Care in Follow-up of Patients With Chronic Conditions

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