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The Virtual Visit for Women With Gestational Diabetes

Primary Purpose

Diabetes, Gestational

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
1-Self-monitoring of blood glucose
2-Self-weighing
3-Self-checking of blood pressure
4-Checking fetal heart rate
5-Visits with caregivers
Sponsored by
Kaiser Permanente
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Diabetes, Gestational

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  1. Diagnosis of gestational diabetes
  2. Singleton pregnancy
  3. <32 weeks gestation
  4. Age 18-45 years
  5. Fluent and literate in English or Spanish
  6. Have a cellphone with capability of internet access.

Exclusion Criteria:

  1. Multiple gestations (twins or higher)
  2. Have a history of fetal demise
  3. Have a history of chronic health problems that might affect outcomes (such as HIV, treatment with steroids, significant cardiac or renal disease, or chronic hypertension), and those who had bariatric surgery.

Sites / Locations

  • Kaiser Permanente Southern California

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Virtual visit

Arm Description

Self-monitoring of blood glucose (four times daily). Self-weighing (weekly). Self-checking of blood pressure (weekly). Checking fetal heart rate (weekly). Visits with caregivers.

Outcomes

Primary Outcome Measures

Compliance With Requirements for Frequency of Glucose Measures
Each patient is requested to check her blood glucose four times a day: fasting and one hour after the first bite of each meal. Compliance with this requirement will be measured for each patient by dividing the number of daily glucose checks actually performed by the number of days in the study.

Secondary Outcome Measures

Compliance With Self-weighing Requirements
Average percentage of weight checks per week in study, calculated as total weight checks in study/weeks in study x 100
Compliance With Blood Pressure Checking Requirements
Percentage of required once-weekly blood pressure checks calculated as total blood pressure checks in study/weeks in study x 100
Glucose Concentrations
Mean of all glucose measures during study, in mg/dl

Full Information

First Posted
October 18, 2016
Last Updated
February 4, 2019
Sponsor
Kaiser Permanente
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1. Study Identification

Unique Protocol Identification Number
NCT02960295
Brief Title
The Virtual Visit for Women With Gestational Diabetes
Official Title
The Virtual Visit for Women With Gestational Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Completed
Study Start Date
September 2014 (undefined)
Primary Completion Date
September 2016 (Actual)
Study Completion Date
September 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Kaiser Permanente

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a feasibility study of care for women with gestational diabetes (GDM) using electronic equipment to participate in virtual office visits. Participants will be trained in the use of glucose meters, scales, and sphygmomanometers which are Bluetooth connected to an app on their cellphones. Fetal well-being will be assessed with Dopplers and kick counts. Care will be delivered by alternate in-office and telephone visits.
Detailed Description
The core elements of a prenatal visit for any pregnant woman include assessment of BP, weight, and presence of fetal heart activity. The treatment of GDM additionally requires the measurement of and review of maternal glycemia. Technology exists for patients to measure these parameters and to relay this information securely directly from these devices via the internet to the healthcare provider's office. A key element of antepartum care for GDM, self-monitoring of blood glucose (SMBG), has for some years been conducted with memory-based portable glucose meters. To assure accuracy in reports of patient measurements, it is important that all devices be of a design wherein results of measures of patient parameters are transmitted in unedited fashion directly devices to the health care provider. While no data exists about the accuracy of self-reporting of patient weight and blood pressure, intentional or unintentional alteration in reports of self-monitored glucose results is a known risk of reliance on patient self-reported data. This pilot study will explore the feasibility of the use of this technology from patients' homes in lieu of an office visit.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Virtual visit
Arm Type
Experimental
Arm Description
Self-monitoring of blood glucose (four times daily). Self-weighing (weekly). Self-checking of blood pressure (weekly). Checking fetal heart rate (weekly). Visits with caregivers.
Intervention Type
Device
Intervention Name(s)
1-Self-monitoring of blood glucose
Intervention Description
Self-monitoring of blood glucose 4 times daily: fasting and 1-hour after each meal. Results will be recorded and transmitted in real-time via a Bluetooth connection to a cellphone app installed on study enrollment. Intervention: At every office visit and at every telephone ("virtual") visit the patient's physician will review glucose results and make adjustments in diet, activity, or medication to bring glucose into desired range.
Intervention Type
Device
Intervention Name(s)
2-Self-weighing
Intervention Description
Self-weighing on electronic scale at least once a week. Results will be recorded and transmitted in real-time via a Bluetooth connection to a cellphone app installed on study enrollment. Consultation with the nutritionist will be obtained for women gaining in excess of or less than that indicated for her pre-pregnancy BMI, per Institute of Medicine (IOM) standards.
Intervention Type
Device
Intervention Name(s)
3-Self-checking of blood pressure
Intervention Description
Self-checking of blood pressure at least weekly with sphygmomanometer. Results will be recorded and transmitted in real-time via a Bluetooth connection to a cellphone app installed on study enrollment. Patients with elevated blood pressure will be requested to come to Obstetrics Triage immediately for further assessment.
Intervention Type
Device
Intervention Name(s)
4-Checking fetal heart rate
Intervention Description
Patient will record her fetus' heart rate with a Doppler device at least once weekly. The patient will immediately report to Labor and Delivery for any fetal heart rate below 100 beats per minute or greater than 160 beats per minute over a 10 minute observation period.Those reporting a fetal heart rate outside of the normal range will be requested to come to ObstetricTriage for further assessment.
Intervention Type
Procedure
Intervention Name(s)
5-Visits with caregivers
Intervention Description
Telephone visits will alternate with in-office visits.Those failing to keep appointments will be contacted and reappointed at a mutually convenient time.
Primary Outcome Measure Information:
Title
Compliance With Requirements for Frequency of Glucose Measures
Description
Each patient is requested to check her blood glucose four times a day: fasting and one hour after the first bite of each meal. Compliance with this requirement will be measured for each patient by dividing the number of daily glucose checks actually performed by the number of days in the study.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Compliance With Self-weighing Requirements
Description
Average percentage of weight checks per week in study, calculated as total weight checks in study/weeks in study x 100
Time Frame
1 year
Title
Compliance With Blood Pressure Checking Requirements
Description
Percentage of required once-weekly blood pressure checks calculated as total blood pressure checks in study/weeks in study x 100
Time Frame
1 year
Title
Glucose Concentrations
Description
Mean of all glucose measures during study, in mg/dl
Time Frame
1 year

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Pregnant women meeting inclusion and exclusion criteria (see below) who volunteer to participate for the study. Volunteers will be solicited sequentially.
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Diagnosis of gestational diabetes Singleton pregnancy <32 weeks gestation Age 18-45 years Fluent and literate in English or Spanish Have a cellphone with capability of internet access. Exclusion Criteria: Multiple gestations (twins or higher) Have a history of fetal demise Have a history of chronic health problems that might affect outcomes (such as HIV, treatment with steroids, significant cardiac or renal disease, or chronic hypertension), and those who had bariatric surgery.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David A Sacks, MD
Organizational Affiliation
Kaiser Permanente
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kaiser Permanente Southern California
City
Pasadena
State/Province
California
ZIP/Postal Code
91101
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
26394017
Citation
Given JE, Bunting BP, O'Kane MJ, Dunne F, Coates VE. Tele-Mum: A Feasibility Study for a Randomized Controlled Trial Exploring the Potential for Telemedicine in the Diabetes Care of Those with Gestational Diabetes. Diabetes Technol Ther. 2015 Dec;17(12):880-8. doi: 10.1089/dia.2015.0147. Epub 2015 Sep 22.
Results Reference
result
PubMed Identifier
22512287
Citation
Homko CJ, Deeb LC, Rohrbacher K, Mulla W, Mastrogiannis D, Gaughan J, Santamore WP, Bove AA. Impact of a telemedicine system with automated reminders on outcomes in women with gestational diabetes mellitus. Diabetes Technol Ther. 2012 Jul;14(7):624-9. doi: 10.1089/dia.2012.0010. Epub 2012 Apr 18.
Results Reference
result
PubMed Identifier
28077459
Citation
Sacks DA, Ling Grant D, Macias M, Li X, Lawrence JM. The Virtual Office Visit for Women With Gestational Diabetes Mellitus. Diabetes Care. 2017 Mar;40(3):e34-e35. doi: 10.2337/dc16-2569. Epub 2017 Jan 11. No abstract available. Erratum In: Diabetes Care. 2019 Apr;42(4):701.
Results Reference
derived

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The Virtual Visit for Women With Gestational Diabetes

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