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Simplification of CF-related Diabetes Screening at Home (AtHome)

Primary Purpose

Cystic Fibrosis, Cystic Fibrosis-related Diabetes

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Standard OGTT
Home-based OGTT (Beverage)
Home-based OGTT (Candy)
Sponsored by
Institut de Recherches Cliniques de Montreal
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Cystic Fibrosis focused on measuring Diabetes, Screening test, Continuous glucose monitoring, Oral glucose tolerance test

Eligibility Criteria

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

Inclusion Criteria:

  • Adult CF-patient without known diabetes
  • In stable condition at least 1-month apart from the last exacerbation.

Exclusion Criteria:

  • Known CFRD
  • Recent exacerbation
  • Use medications known to interfere with glucose metabolism such as oral steroids.

Sites / Locations

  • CHUM
  • Montreal Clinical Research Institute (IRCM)

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Other

Experimental

Experimental

Arm Label

Standard OGTT

Home-based OGTT (Beverage)

Home-based OGTT (Candy)

Arm Description

OGTT standard test at hospital (75g glucose beverage; 2-h test with plasma glucose collection)

Home-based OGTT with CGM device, without glucose collection (75g glucose beverage; 2-h test: glycemia measured by CGM)

Home-based OGTT with CGM device, without glucose collection (75g of glucose (Jelly Beans); 2-h test: glycemia measured by CGM)

Outcomes

Primary Outcome Measures

Internal validity
Specificity and sensitivity of both home-based OGTTs versus a standard OGTT in controlled setting
Predictive value (positive and negative)
Both home-based OGTTs versus a standard OGTT in controlled setting

Secondary Outcome Measures

Patient's perception
Visual analog scale questionnaire
Cost evaluation of methods
Estimated cost of each methods

Full Information

First Posted
July 18, 2017
Last Updated
June 24, 2020
Sponsor
Institut de Recherches Cliniques de Montreal
Collaborators
Université de Montréal, Vertex Pharmaceuticals Incorporated
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1. Study Identification

Unique Protocol Identification Number
NCT03227094
Brief Title
Simplification of CF-related Diabetes Screening at Home
Acronym
AtHome
Official Title
Simplification of CF-related Diabetes Screening by the Use of a Home-based Oral Glucose Tolerance Test (OGTT): A Pilot Study to Evaluate the Validity and Patients' Perceptions
Study Type
Interventional

2. Study Status

Record Verification Date
June 2020
Overall Recruitment Status
Completed
Study Start Date
November 13, 2017 (Actual)
Primary Completion Date
April 1, 2020 (Actual)
Study Completion Date
April 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Institut de Recherches Cliniques de Montreal
Collaborators
Université de Montréal, Vertex Pharmaceuticals Incorporated

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
Cystic fibrosis (CF)-related diabetes (CFRD) is the most common complication after pulmonary complications. This specific form of diabetes is associated with an increased morbidity and mortality. CFRD prevalence at the age of 10 is 10% and reaches 40 to 50% in adulthood, while another 35% of adult patients presents impaired glucose tolerance. In order to identify patients at risk and to implement early therapeutic measures, an annual CFRD screening test should therefore be undertaken for CF patients after 10 years of age. The 2-hour oral glucose tolerance test (OGTT) with a sweet beverage is the recommended screening test. However, participation rates for screening tests are far from optimal. For examples, in 2015, the investigators observed that only 47% of non-diabetic patients attended to planned screening despite large availability and advertisement (unpublished data). Comparable low levels of screening for CFRD, usually below 33%, have been reported by various teams. Several reasons could explain these low adherence rates. Some factors are related to patients perceptions and experience: OGTT is perceived as an additional medical burden requiring a scheduled appointment (several weeks after the last exacerbation); overnight fasting followed by the intake of a large glucose load within 5 minutes can lead to nausea, headache, bloating and fatigue; some patients fear multiple blood sampling, etc. In addition, in case of CFRD diagnosis, recommended capillary blood glucose monitoring, nutritional advice and treatment (insulin) are perceived as extremely invasive and complex, thus some patients prefer avoiding screening test. To date, no alternative screening method has demonstrated its effectiveness to screen for CFRD. The investigators of this study believe that a simplified version of the OGTT would be more attractive, would make it more acceptable for patients and has the potential to improve their adherence to screening tests, simplify CF-team works and reduce costs. By allowing appropriate education and introduction of treatment in a timely manner, improved adherence to annual screening for dysglycemia has the potential to minimize or prevent clinical deterioration observed in years preceding CFRD onset.
Detailed Description
The investigators propose a pilot study to evaluate the validity and the acceptability of a home-based OGTT by comparing, in patients with CF: Standard hospital-based OGTT with measures of plasma glucose and the use of 75g glucose beverage; Home-based OGTT with measures of glucose using a continuous glucose monitoring system (CGMS; without blood sample collection) and the 75g glucose beverage; Home-based OGTT with measures of glucose using CGMS and 75g of glucose from candies as a substitute to this poorly appreciate beverage. Specific objectives are to determine i) the internal validity (specificity, sensitivity) of both home-based OGTTs versus a standard OGTT in controlled setting, and ii) the predictive value (positive and negative). The investigators will also iii) investigate patient's perception and likelihood that the proposed method improves adherence to annual screening, and iv) evaluate potential cost reduction associated with proposed simplified screening tests. On the day of the OGTT, and after obtaining informed consent, a CGMS will be installed. Patients will receive the very simple training required to use it as well as a pre-packed Jelly Beans bag containing 75g of glucose and a standard 75g glucose beverage bottle. This CGMS will provide interstitial glucose values each 15 min over the next 14 days.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis, Cystic Fibrosis-related Diabetes
Keywords
Diabetes, Screening test, Continuous glucose monitoring, Oral glucose tolerance test

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
37 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard OGTT
Arm Type
Other
Arm Description
OGTT standard test at hospital (75g glucose beverage; 2-h test with plasma glucose collection)
Arm Title
Home-based OGTT (Beverage)
Arm Type
Experimental
Arm Description
Home-based OGTT with CGM device, without glucose collection (75g glucose beverage; 2-h test: glycemia measured by CGM)
Arm Title
Home-based OGTT (Candy)
Arm Type
Experimental
Arm Description
Home-based OGTT with CGM device, without glucose collection (75g of glucose (Jelly Beans); 2-h test: glycemia measured by CGM)
Intervention Type
Diagnostic Test
Intervention Name(s)
Standard OGTT
Intervention Description
Standard-OGTT Plasma glucose : 0, 30, 60, 90, 120 minutes Complete biochemical profile, weight and size (body mass index), drugs list, pulmonary function by spirometry (FEV, etc.) Questionnaires CGMS training & delivery of Jelly-Bean/75g glucose beverage
Intervention Type
Diagnostic Test
Intervention Name(s)
Home-based OGTT (Beverage)
Intervention Description
In a random order Candy-OGTT (Jelly-Bean) or 75 g glucose beverage Glycemia every 15 minutes from CGMS collection; standardized condition (fasting + rest) Questionnaires
Intervention Type
Diagnostic Test
Intervention Name(s)
Home-based OGTT (Candy)
Intervention Description
In a random order Candy-OGTT (Jelly-Bean) or 75 g glucose beverage Glycemia every 15 minutes from CGMS collection; standardized condition (fasting + rest) Questionnaires
Primary Outcome Measure Information:
Title
Internal validity
Description
Specificity and sensitivity of both home-based OGTTs versus a standard OGTT in controlled setting
Time Frame
OGTTs performed within 14 days
Title
Predictive value (positive and negative)
Description
Both home-based OGTTs versus a standard OGTT in controlled setting
Time Frame
OGTTs performed within 14 days
Secondary Outcome Measure Information:
Title
Patient's perception
Description
Visual analog scale questionnaire
Time Frame
OGTTs performed within 14 days
Title
Cost evaluation of methods
Description
Estimated cost of each methods
Time Frame
OGTTs performed within 14 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult CF-patient without known diabetes In stable condition at least 1-month apart from the last exacerbation. Exclusion Criteria: Known CFRD Recent exacerbation Use medications known to interfere with glucose metabolism such as oral steroids.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rémi Rabasa-Lhoret, MD, PhD
Organizational Affiliation
Montreal Research Clinical Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHUM
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H2W1R7
Country
Canada
Facility Name
Montreal Clinical Research Institute (IRCM)
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H2W 1R7
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No

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Simplification of CF-related Diabetes Screening at Home

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