eHealth Intervention on Physical Activity for Type 2 Diabetics - Frustrated by COVID-19 (MySteps-CoV)
Primary Purpose
Type2 Diabetes
Status
Unknown status
Phase
Not Applicable
Locations
Finland
Study Type
Interventional
Intervention
eHealth +counselling contacts
eHealth
Usual care
Sponsored by
About this trial
This is an interventional supportive care trial for Type2 Diabetes focused on measuring physical activity, sedentary behavior, accelerometer, eHealth, COVID-19
Eligibility Criteria
Inclusion Criteria:
- a diagnosed type 2 diabetes
- a prescheduled appointment with a health care professional regarding PA counselling in primary care settings of North Karelia Hospital District, Finland
- body mass index <40
- does not meet the current PA recommendation for health
- is able to conduct six minute walk test.
Exclusion Criteria:
- any problem that limits ability to walk without an aid
- any health problem that hinders participation in light to moderate intensity PA,
- not able or willing to use smartphone
- not willing to wear the research accelerometer at the baseline
Sites / Locations
- North Karelia Hospital District
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Other
Arm Label
eHealth + counselling contacts
eHealth
Usual care
Arm Description
6-month eHealth physical activity intervention complemented by face-to-face and telephone counselling contacts on physical activity..
6-month eHealth physical activity intervention
Usual care of type 2 diabetics within the primary health care setting.
Outcomes
Primary Outcome Measures
Change in total mean daily step count
Step count during one week is measured with a hip-worn accelerometer at baseline, 6 months, and 12 months
Secondary Outcome Measures
Changes in total mean daily time of sedentary, low intensity PA and moderate-to-vigorous PA
Sedentary time and PA time at different intensity ranges are measured with a hip-worn accelerometer at baseline, 6 months and 12 months
Changes in the mean daily number of moderate-to-vigorous PA bouts lasting at least 1, 5 and 10 minutes.
Durations of moderate-to-vigorous PA bouts measured with a hip-worn accelerometer at baseline, 6 months and 12 months
Full Information
NCT ID
NCT04587414
First Posted
September 8, 2020
Last Updated
October 13, 2020
Sponsor
UKK Institute
Collaborators
North Karelia Hospital District, University of Eastern Finland
1. Study Identification
Unique Protocol Identification Number
NCT04587414
Brief Title
eHealth Intervention on Physical Activity for Type 2 Diabetics - Frustrated by COVID-19
Acronym
MySteps-CoV
Official Title
Personalized eHealth Intervention in Patients With Type 2 Diabetes to Promote Daily Physical Activity Utilizing 24h Self-monitoring - Implementation Frustrated by COVID-19 Epidemic
Study Type
Interventional
2. Study Status
Record Verification Date
October 2020
Overall Recruitment Status
Unknown status
Study Start Date
March 6, 2019 (Actual)
Primary Completion Date
October 31, 2020 (Anticipated)
Study Completion Date
October 31, 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
UKK Institute
Collaborators
North Karelia Hospital District, University of Eastern Finland
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
This pragmatic 3-arm randomized controlled trial is conducted within the primary health care setting. The trial evaluates the effectiveness of a personalized eHealth intervention based on a hip-worn accelerometer, smartphone application and cloud service (www.exced.com) with or without face-to-face and telephone counselling contacts on physical activity (PA) compared to usual care in increasing daily PA and reducing sedentary behavior (SB) among type 2 diabetes (T2D) patients.The duration of the intervention period is 6 months, after which there is a 6 month follow-up for evaluating the maintenance of anticipated intervention effects. The primary goal of the intervention is that the T2D patients increase their daily number of steps by replacing SB with low intensity PA. The secondary goal is to increase short bouts of moderate-to-vigorous PA according to personal goals. It is expected that the eHealth intervention complemented by individual counselling is the most effective in reaching the goals, and the eHealth intervention is more effective than usual care.
Measurements are done at baseline, after the 6-month intervention, and after the 6-month follow-up. Participants' one-week PA and SB are measured with a hip-worn triaxial accelerometer and analyzed with validated algorithms. Cardiorespiratory fitness is assessed with a validated 6-minute walk test. Diabetes-related metabolic biomarkers (HbA1C, LDL-c, HDL-c, oxidized LDL and HDL lipids) and cardiovascular risk factors (blood pressure, BMI, waist circumference) are measured with standard laboratory methods. Quality of life is assessed by RAND-36 method. The interventions are evaluated with RE-AIM (Reach, Effectiveness, Adoption, Implementation and Maintenance) method. Besides effectiveness, RE-AIM methods evaluates the target group reach and adherence; provider adoption; intervention fidelity; maintenance of the changes in PA and SB behavior, biomarkers and CVD risk factors; intervention transferability to clinical practice; adverse events; and patient and provider satisfaction.
Unexpectedly, the COVID-19 pandemic in spring 2020 led to substantial restrictions in outdoors mobility of T2D patients and their access access to health care in Finland, facts that frustrated the planned implementation of the original intervention, related measurements and their scheduling. This means that not all planned measurements could be done at all or at the scheduled time point. Irrespective of the time of recruitment, all follow-up measurements are done from June to September 2020. Notwithstanding the COVID-19 pandemic annulled the original intervention, the collected data yet provides unique insights into measured physical activity, fitness and metabolic biomarkers of T2D patients before and during the COVID-19 pandemic and consequent restrictions.In addition, the data allows to evaluate the implementation of eHealth approach and face-to-face and telephone PA counselling contacts within the primary health care setting.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type2 Diabetes
Keywords
physical activity, sedentary behavior, accelerometer, eHealth, COVID-19
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The study is a pragmatic three-arm randomized controlled trial carried out within the primary health care setting. Besides the usual care given to type 2 diabetics, the patients may be assigned either into a 6-month eHealth intervention complemented by face-to-face and telephone counselling contacts on physical activity or into a 6-month eHealth intervention without counselling contacts. After the 6-month intervention, there is a 6-month follow-up period.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
122 (Actual)
8. Arms, Groups, and Interventions
Arm Title
eHealth + counselling contacts
Arm Type
Experimental
Arm Description
6-month eHealth physical activity intervention complemented by face-to-face and telephone counselling contacts on physical activity..
Arm Title
eHealth
Arm Type
Experimental
Arm Description
6-month eHealth physical activity intervention
Arm Title
Usual care
Arm Type
Other
Arm Description
Usual care of type 2 diabetics within the primary health care setting.
Intervention Type
Behavioral
Intervention Name(s)
eHealth +counselling contacts
Intervention Description
The 6 month eHealth intervention comprises continuous self-monitoring of PA and SB using hip-worn accelerometer and ExSed application, which gives cloud-computed personal feedback about accelerometer-measured PA and SB on smartphone and provides a platform for a health care professional to set and monitor patient's personal activity goals as well as give personalized feedback to the patient. In addition, instructions and video-demonstrations on how to reach the goals are provided via Internet. The eHealth intervention is complemented by face-to-face and telephone counselling on physical activity which comprises 4 to 6 contacts between a health care professional and the patient as well as at least 3 telephone contacts during 6 months.
Intervention Type
Behavioral
Intervention Name(s)
eHealth
Intervention Description
The 6 month eHealth intervention comprises continuous self-monitoring of PA and SB using hip-worn accelerometer and ExSed application, which gives cloud-computed personal feedback about accelerometer-measured PA and SB on smartphone and provides a platform for a health care professional to set and monitor patient's personal activity goals as well as give personalized feedback to the patient. In addition, instructions and video-demonstrations on how to reach the goals are provided via Internet. No telephone calls nor face-to-face counselling contacts on physical activity are taken.
Intervention Type
Behavioral
Intervention Name(s)
Usual care
Intervention Description
Usual care and councelling given to type 2 diabetics within the primary health care setting.
Primary Outcome Measure Information:
Title
Change in total mean daily step count
Description
Step count during one week is measured with a hip-worn accelerometer at baseline, 6 months, and 12 months
Time Frame
At 6 and 12 months compared to baseline (0 months). N.B. Because of COVID-19, the schedule and contents of measurements may change individually depending on the time of recruitment.
Secondary Outcome Measure Information:
Title
Changes in total mean daily time of sedentary, low intensity PA and moderate-to-vigorous PA
Description
Sedentary time and PA time at different intensity ranges are measured with a hip-worn accelerometer at baseline, 6 months and 12 months
Time Frame
at 6 and 12 months compared to baseline (0 months). N.B. Because of COVID-19, the schedule and contents of measurements may change individually depending on the time of recruitment.
Title
Changes in the mean daily number of moderate-to-vigorous PA bouts lasting at least 1, 5 and 10 minutes.
Description
Durations of moderate-to-vigorous PA bouts measured with a hip-worn accelerometer at baseline, 6 months and 12 months
Time Frame
at 6 and 12 months compared to baseline (0 months). N.B. Because of COVID-19, the schedule and contents of measurements may change individually depending on the time of recruitment.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
69 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
a diagnosed type 2 diabetes
a prescheduled appointment with a health care professional regarding PA counselling in primary care settings of North Karelia Hospital District, Finland
body mass index <40
does not meet the current PA recommendation for health
is able to conduct six minute walk test.
Exclusion Criteria:
any problem that limits ability to walk without an aid
any health problem that hinders participation in light to moderate intensity PA,
not able or willing to use smartphone
not willing to wear the research accelerometer at the baseline
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tommi Vasankari, MD, PhD
Organizational Affiliation
UKK Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
North Karelia Hospital District
City
Joensuu
ZIP/Postal Code
80210
Country
Finland
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
eHealth Intervention on Physical Activity for Type 2 Diabetics - Frustrated by COVID-19
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