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Efficacy of a Virtual Care Clinic in the Management of Diabetes Mellitus

Primary Purpose

Diabetes Mellitus

Status
Terminated
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Virtual Care
Standard of Care
Sponsored by
Endocrine Research Society
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus

Eligibility Criteria

19 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Type 2 Diabetes
  • Access and the ability to use the internet on a computer or mobile device
  • Access to a family physician and lab for blood tests

Exclusion Criteria:

  • Patients that are pregnant or attempting to conceive
  • Liver disease (AST or ALT levels >2.5 times the reference level)
  • Renal insufficient with a serum creatine level >200 umol/L
  • Patients who see an endocrinologist or diabetes specialist within their community

Sites / Locations

  • Endocrine Research Society

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Interventional Group

Standard of Care

Arm Description

The recruited participants will be provided access to Virtual Care suite via internet and telephone communication.

The recruited participants will receive the standard of diabetes care as offered by the services in their community.

Outcomes

Primary Outcome Measures

HbA1c
Routine blood work measuring average blood sugar levels, at total of two tests will be preformed at three month intervals over the 6 month study period. Baseline A1C at recruitment will also be included in analysis.

Secondary Outcome Measures

Survey of Healthcare Utilization
At the start and end of study (six months), participants will complete a self-reported survey of their utilization of healthcare services, including hospitalizations, physician visits, intervention website visits, perceived medication changes.
Survey of Quality of Life
At the start and end of study (six months), participants will complete the Audit for Diabetes Dependent Quality of Life survey.

Full Information

First Posted
January 19, 2016
Last Updated
September 18, 2023
Sponsor
Endocrine Research Society
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1. Study Identification

Unique Protocol Identification Number
NCT02681185
Brief Title
Efficacy of a Virtual Care Clinic in the Management of Diabetes Mellitus
Official Title
Efficacy of a Virtual Care Clinic in the Management of Diabetes Mellitus
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Terminated
Why Stopped
enrollment not satisfied
Study Start Date
March 1, 2018 (Actual)
Primary Completion Date
July 4, 2023 (Actual)
Study Completion Date
July 4, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Endocrine Research Society

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 study's goal is to promote accessible and cost-effective diabetes care through electronic means. Underserved populations including rural areas do not have diabetes specialists. Previous study data has shown the effectiveness of Internet communication in lowering a patient's Hemoglobin A1C, a measure of blood sugars, closer to the target number. The investigators thus wish to test the effectiveness of diabetes care provided by virtual means, including virtual consultations, online monitoring of blood sugars, diabetes education via web-based videos, and support/advice provided through phone or email by an Endocrinologist. The goal is to test if virtual care is a viable means to extend care for diabetes to underserved populations.
Detailed Description
Purpose To determine if a virtual-care based system can effectively provide care for patients with diabetes. Hypothesis Alternative: Virtual-care is associated with achieving glycemic control in patients with diabetes. Null: Virtual-care is not associated with achieving glycemic control in patients with diabetes. Justification The potential study participants would normally receive care from a primary care physician and have no access to a diabetes specialist. In the study, they would have access to an Endocrinologist through online communication and by telephone. Objectives The primary end-point is to determine if patients using virtual care have reduced HbA1c values at followup. The data may be used to write a white paper guiding diabetes treatment guidelines within the province of British Columbia, Canada. The goal is for diabetes specialists to be able to provide care to underserved areas without requiring to be physically at the location. Research Method Participants satisfying the inclusion criteria will be recruited and followed for six months. Their family physician or Diabetes Center will provide a referral to one of the investigators, who are diabetes specialists, for a virtual consult via telephone. Relevant medical records will be transferred for this consult. After the consult, participants will be asked to submit self-monitored blood glucose levels via email to the diabetes specialists for follow-up every two weeks. These follow-up reports may lead to the diabetes specialists making adjustments to therapy. Concurrently, the participants during the followup period will be provided access to a free website containing modules on diabetes education similar to a diabetes clinic education program. They will be allowed to view them at their own discretion.. Every 3 months participants will be asked to have regular blood work done to assess management, including A1C levels. This is part of routine care, but the data will be used for analysis. Statistical Analysis Outcomes will be tested for significant differences via t tests, as well as the other clinical measures, while the summarized survey responses will be tallied and tested for correlation with changes in clinical measures. The planned sample size of 100 was estimated from previous studies' mean changes in A1C and standard deviations involving similar methods. For calculating the sample size, a statistical power of 0.80 and alpha of 0.05 were used.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Experimental vs. Standard of Care
Masking
None (Open Label)
Allocation
Randomized
Enrollment
11 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Interventional Group
Arm Type
Experimental
Arm Description
The recruited participants will be provided access to Virtual Care suite via internet and telephone communication.
Arm Title
Standard of Care
Arm Type
Active Comparator
Arm Description
The recruited participants will receive the standard of diabetes care as offered by the services in their community.
Intervention Type
Other
Intervention Name(s)
Virtual Care
Intervention Description
Virtual Care consists of the following services and resources: Have a virtual consult through online methods or telephone with one of the study endocrinologists Be encouraged to report blood sugar readings every 2 weeks to their endocrinologist for regular follow-up and feedback via online methods Be given access to a website with modules that attempt to replicate the information learned in a diabetes teaching clinic Be given access to a certified diabetes educator through online methods or telephone. This will cover any other information that cannot be personalized on the teaching website, such as specific diet advice and social support.
Intervention Type
Other
Intervention Name(s)
Standard of Care
Intervention Description
Standard of care offered in the patient's community. May involve in-person education at a diabetes centre and consultation with a healthcare professional.
Primary Outcome Measure Information:
Title
HbA1c
Description
Routine blood work measuring average blood sugar levels, at total of two tests will be preformed at three month intervals over the 6 month study period. Baseline A1C at recruitment will also be included in analysis.
Time Frame
3 month intervals for 6 months
Secondary Outcome Measure Information:
Title
Survey of Healthcare Utilization
Description
At the start and end of study (six months), participants will complete a self-reported survey of their utilization of healthcare services, including hospitalizations, physician visits, intervention website visits, perceived medication changes.
Time Frame
Start and End of study (six months)
Title
Survey of Quality of Life
Description
At the start and end of study (six months), participants will complete the Audit for Diabetes Dependent Quality of Life survey.
Time Frame
Start and End of study (six months)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Type 2 Diabetes Access and the ability to use the internet on a computer or mobile device Access to a family physician and lab for blood tests Exclusion Criteria: Patients that are pregnant or attempting to conceive Liver disease (AST or ALT levels >2.5 times the reference level) Renal insufficient with a serum creatine level >200 umol/L Patients who see an endocrinologist or diabetes specialist within their community
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adam White, MD
Organizational Affiliation
Clinical Associate Professor, UBC
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Monika Pawlowska, MD
Organizational Affiliation
Clinical Assistant Professor, UBC
Official's Role
Principal Investigator
Facility Information:
Facility Name
Endocrine Research Society
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V6J4Y3
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Data collected during the study will be stored on study site in an encrypted format, all data pertaining to individual patients will be available only to the study investigators.
Citations:
PubMed Identifier
16371630
Citation
Nathan DM, Cleary PA, Backlund JY, Genuth SM, Lachin JM, Orchard TJ, Raskin P, Zinman B; Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Study Research Group. Intensive diabetes treatment and cardiovascular disease in patients with type 1 diabetes. N Engl J Med. 2005 Dec 22;353(25):2643-53. doi: 10.1056/NEJMoa052187.
Results Reference
background
PubMed Identifier
9742976
Citation
Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). UK Prospective Diabetes Study (UKPDS) Group. Lancet. 1998 Sep 12;352(9131):837-53. Erratum In: Lancet 1999 Aug 14;354(9178):602.
Results Reference
background
PubMed Identifier
18937550
Citation
Hirsch IB, Bode BW, Childs BP, Close KL, Fisher WA, Gavin JR, Ginsberg BH, Raine CH, Verderese CA. Self-Monitoring of Blood Glucose (SMBG) in insulin- and non-insulin-using adults with diabetes: consensus recommendations for improving SMBG accuracy, utilization, and research. Diabetes Technol Ther. 2008 Dec;10(6):419-39. doi: 10.1089/dia.2008.0104.
Results Reference
background
PubMed Identifier
17102152
Citation
Austin MM, Haas L, Johnson T, Parkin CG, Parkin CL, Spollett G, Volpone MT. Self-monitoring of blood glucose: benefits and utilization. Diabetes Educ. 2006 Nov-Dec;32(6):835-6, 844-7. doi: 10.1177/0145721706295873. No abstract available.
Results Reference
background
PubMed Identifier
20668152
Citation
Tildesley HD, Mazanderani AB, Ross SA. Effect of Internet therapeutic intervention on A1C levels in patients with type 2 diabetes treated with insulin. Diabetes Care. 2010 Aug;33(8):1738-40. doi: 10.2337/dc09-2256.
Results Reference
background
PubMed Identifier
24500556
Citation
Tildesley HD, Wright AM, Chan JH, Mazanderani AB, Ross SA, Tildesley HG, Lee AM, Tang TS, White AS. A comparison of internet monitoring with continuous glucose monitoring in insulin-requiring type 2 diabetes mellitus. Can J Diabetes. 2013 Oct;37(5):305-8. doi: 10.1016/j.jcjd.2013.05.006.
Results Reference
background
PubMed Identifier
24459161
Citation
Tildesley HD, Conway ME, Ross SA, Lee AM, Chan JH, Mazanderani AB, Tildesley HG, White AS. Review of the effect of internet therapeutic intervention in patients with type 1 and type 2 diabetes. Diabetes Care. 2014 Feb;37(2):e31-2. doi: 10.2337/dc13-1940. No abstract available.
Results Reference
background
PubMed Identifier
25456641
Citation
Tildesley HD, Po MD, Ross SA. Internet blood glucose monitoring systems provide lasting glycemic benefit in type 1 and 2 diabetes: a systematic review. Med Clin North Am. 2015 Jan;99(1):17-33. doi: 10.1016/j.mcna.2014.08.019. Epub 2014 Oct 18.
Results Reference
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Efficacy of a Virtual Care Clinic in the Management of Diabetes Mellitus

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