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

Sponsor
Endocrine Research Society (Other)
Overall Status
Recruiting
CT.gov ID
NCT02681185
Collaborator
(none)
100
1
2
88
1.1

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Virtual Care
  • Other: Standard of Care
N/A

Detailed Description

  1. Purpose To determine if a virtual-care based system can effectively provide care for patients with diabetes.

  2. 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.

  1. 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.

  2. 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.

  3. 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.

  1. 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Experimental vs. Standard of CareExperimental vs. Standard of Care
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Efficacy of a Virtual Care Clinic in the Management of Diabetes Mellitus
Actual Study Start Date :
Mar 1, 2018
Anticipated Primary Completion Date :
Jul 1, 2025
Anticipated Study Completion Date :
Jul 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Interventional Group

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

Other: Virtual Care
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.

Active Comparator: Standard of Care

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

Other: Standard of Care
Standard of care offered in the patient's community. May involve in-person education at a diabetes centre and consultation with a healthcare professional.

Outcome Measures

Primary Outcome Measures

  1. HbA1c [3 month intervals for 6 months]

    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

  1. Survey of Healthcare Utilization [Start and End of study (six months)]

    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.

  2. Survey of Quality of Life [Start and End of study (six months)]

    At the start and end of study (six months), participants will complete the Audit for Diabetes Dependent Quality of Life survey.

Eligibility Criteria

Criteria

Ages Eligible for Study:
19 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Endocrine Research Society Vancouver British Columbia Canada V6J4Y3

Sponsors and Collaborators

  • Endocrine Research Society

Investigators

  • Principal Investigator: Adam White, MD, Clinical Associate Professor, UBC
  • Principal Investigator: Monika Pawlowska, MD, Clinical Assistant Professor, UBC

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
ERS Gap Student, Clinical Professor, Endocrine Research Society
ClinicalTrials.gov Identifier:
NCT02681185
Other Study ID Numbers:
  • Virtual Care
First Posted:
Feb 12, 2016
Last Update Posted:
Jul 27, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 27, 2022