SPARK- a Digital Platform to Improve Self-management of Gestational Diabetes (SPARK)
Primary Purpose
Gestational Diabetes Mellitus
Status
Recruiting
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
SPARK
Sponsored by
About this trial
This is an interventional treatment trial for Gestational Diabetes Mellitus
Eligibility Criteria
Inclusion Criteria:
- a confirmed diagnosis of GDM detected by oral glucose tolerance test in accordance with the World Health Organization guidelines
Exclusion Criteria:
- known pre-pregnancy diabetes
- twin pregnancy
- <18 years of age
- severe co-morbidities that would limit participation or a previously diagnosed severe psychiatric illness.
Sites / Locations
- Maternity health care, Region ÖstergötlandRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
SPARK app
Control arm
Arm Description
Access to the SPARK app which will provide support for a healthier diet and increased physical activity as well as daily monitoring of blood glucose levels.
Standard care i.e., the routine treatment program for GDM delivered by the care provider.
Outcomes
Primary Outcome Measures
Glucose control
Time in Range percent of time for glucose levels within clinical target levels using continous glucose monitoring
HbA1c
Glycosylated hemoglobulin
Secondary Outcome Measures
Diet intake quality using three dietary recalls by means of the Riksmaten Flex method
Diet intake quality will be assessed using three 24 hour dietary recalls by means of the Riksmaten Flex web-based dietary recall method.
Physical activity using accelerometry
Time spent on physical activity at different levels (sedentary, light, moderate, vigorous) in minutes per day will be assessed using accelerometry collected during 7 days
Incidence of pre-eclampsia
Diagnosis of pre-eclampsia
Incidence of Caesarean sections
Delivery by caesarean sections
Incidence of pregnancy induced hypertension
Diagnosis of pregnancy induced hypertension
Metformin/insulin treatment
Introduction of metformin/insulin treatment
Preterm birth
Delivery before 37 completed weeks
Gestational weight gain
Increase in body weight during pregnancy
Infant birth weight
Infant birth weight in grams
Infant birth length
Infant birth length in centimetres
Infant Apgar score
Infant Apgar score at 1, 5 and 10 min
Incidence of large-for gestational-age infant
Birth weight >90th percentile for gestational age and gender
Infant shoulder dystocia
Incidence of infant shoulder dystocia
Infant hypoglycaemia
Incidence of infant hypoglycaemia
Glucose control
Time in Range percent of time for glucose levels above and below clinical target levels using continous glucose monitoring
Glycaemic variability I
Coefficient of variation for glucose excursion over 24 hrs using continous glucose monitoring
Glycaemic variability II
Mean for glucose excursion over 24 hrs using continous glucose monitoring
Delivery complications
Induction of delivery (yes or no), vacuum extraction (yes or no, epidural anesthesia (yes or no)
Hospital stay
Hospital stay (duration from admission of delivery to discharge) including neonatal care
Glucose- insulin treatment during delivery
Incidence of glucose- insulin treatment during delivery
Metabolic and inflammatory biomarkers I
Maternal levels of Insulin-like Growth Factor I in serum
Metabolic and inflammatory biomarkers II
Maternal levels of Insulin-like Growth Factor I binding proteins in serum
Metabolic and inflammatory biomarkers III
Maternal levels of copeptin in serum
Metabolic and inflammatory biomarkers IV
Maternal levels of leptin in serum
Metabolic and inflammatory biomarkers V
Maternal levels of midregion pro-adrenomedullin (MR-proANP) in serum
Maternal cardiometabolic risk profile
A maternal cardiometabolic risk profile score one year post partum will be calculated using information on triglycerides and high-density cholesterol in serum, waist circumference, blood glucose as well as the systolic and diastolic blood pressure.
Full Information
NCT ID
NCT05348863
First Posted
April 13, 2022
Last Updated
October 28, 2022
Sponsor
Karolinska Institutet
Collaborators
Region Östergötland, Linkoeping University
1. Study Identification
Unique Protocol Identification Number
NCT05348863
Brief Title
SPARK- a Digital Platform to Improve Self-management of Gestational Diabetes
Acronym
SPARK
Official Title
SPARK: Smart Phone App for Gestational Diabetes Patients Supporting Key Lifestyle Behaviors and Glucose Control
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
October 28, 2022 (Actual)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
December 30, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet
Collaborators
Region Östergötland, Linkoeping University
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
Gestational diabetes mellitus (GDM) is an increasing public health challenge. Innovative, effective and scalable lifestyle interventions to support women with GDM to manage their disease and to prevent adverse obstetric and neonatal outcomes as well as later morbidity are requested.The aim of this project is to evaluate whether a novel, mobile health (mHealth) platform (SPARK) can improve self-management of GDM and prevent adverse maternal and offspring outcomes. SPARK is a multi-centre randomised controlled trial recruiting women diagnosed with GDM in South Eastern Sweden. Women will be randomised to the control or intervention group. All women will receive standard care. The intervention group will also receive support through the SPARK platform for healthy eating, physical activity and glycaemic control. Pregnancy outcomes are glycaemic control (primary), diet, physical activity, metabolic and inflammatory biomarkers in gestational week 36-37 as well as adverse obstetric and neonatal outcomes. Secondary outcomes also include cardiometabolic risk, physical activity and healthy eating behaviours one-year postpartum.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gestational Diabetes Mellitus
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
360 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
SPARK app
Arm Type
Experimental
Arm Description
Access to the SPARK app which will provide support for a healthier diet and increased physical activity as well as daily monitoring of blood glucose levels.
Arm Title
Control arm
Arm Type
No Intervention
Arm Description
Standard care i.e., the routine treatment program for GDM delivered by the care provider.
Intervention Type
Behavioral
Intervention Name(s)
SPARK
Intervention Description
The SPARK digital platform provides support to the patient (shown as an app) as well as provides the possibility for the health care provider to review and give feedback on blood glucose levels through the care giver interface of the platform.
Primary Outcome Measure Information:
Title
Glucose control
Description
Time in Range percent of time for glucose levels within clinical target levels using continous glucose monitoring
Time Frame
At the end of the intervention in gestational weeks 36-37
Title
HbA1c
Description
Glycosylated hemoglobulin
Time Frame
At the end of the intervention in gestational weeks 36-37
Secondary Outcome Measure Information:
Title
Diet intake quality using three dietary recalls by means of the Riksmaten Flex method
Description
Diet intake quality will be assessed using three 24 hour dietary recalls by means of the Riksmaten Flex web-based dietary recall method.
Time Frame
At the end of the intervention in gestational weeks 36-37
Title
Physical activity using accelerometry
Description
Time spent on physical activity at different levels (sedentary, light, moderate, vigorous) in minutes per day will be assessed using accelerometry collected during 7 days
Time Frame
At the end of the intervention in gestational weeks 36-37
Title
Incidence of pre-eclampsia
Description
Diagnosis of pre-eclampsia
Time Frame
Up to delivery
Title
Incidence of Caesarean sections
Description
Delivery by caesarean sections
Time Frame
Up to delivery
Title
Incidence of pregnancy induced hypertension
Description
Diagnosis of pregnancy induced hypertension
Time Frame
Up to delivery
Title
Metformin/insulin treatment
Description
Introduction of metformin/insulin treatment
Time Frame
Up to delivery
Title
Preterm birth
Description
Delivery before 37 completed weeks
Time Frame
Up to delivery
Title
Gestational weight gain
Description
Increase in body weight during pregnancy
Time Frame
From pre-prepregnancy up to 40 weeks of gestation
Title
Infant birth weight
Description
Infant birth weight in grams
Time Frame
At birth
Title
Infant birth length
Description
Infant birth length in centimetres
Time Frame
At birth
Title
Infant Apgar score
Description
Infant Apgar score at 1, 5 and 10 min
Time Frame
At birth
Title
Incidence of large-for gestational-age infant
Description
Birth weight >90th percentile for gestational age and gender
Time Frame
At birth
Title
Infant shoulder dystocia
Description
Incidence of infant shoulder dystocia
Time Frame
At birth
Title
Infant hypoglycaemia
Description
Incidence of infant hypoglycaemia
Time Frame
At birth
Title
Glucose control
Description
Time in Range percent of time for glucose levels above and below clinical target levels using continous glucose monitoring
Time Frame
At the end of the intervention in gestational week 36-37
Title
Glycaemic variability I
Description
Coefficient of variation for glucose excursion over 24 hrs using continous glucose monitoring
Time Frame
At the end of the intervention in gestational week 36-37
Title
Glycaemic variability II
Description
Mean for glucose excursion over 24 hrs using continous glucose monitoring
Time Frame
At the end of the intervention in gestational week 36-37
Title
Delivery complications
Description
Induction of delivery (yes or no), vacuum extraction (yes or no, epidural anesthesia (yes or no)
Time Frame
At delivery
Title
Hospital stay
Description
Hospital stay (duration from admission of delivery to discharge) including neonatal care
Time Frame
The first week post partum
Title
Glucose- insulin treatment during delivery
Description
Incidence of glucose- insulin treatment during delivery
Time Frame
During delivery
Title
Metabolic and inflammatory biomarkers I
Description
Maternal levels of Insulin-like Growth Factor I in serum
Time Frame
At gestational weeks 36-37
Title
Metabolic and inflammatory biomarkers II
Description
Maternal levels of Insulin-like Growth Factor I binding proteins in serum
Time Frame
At gestational weeks 36-37
Title
Metabolic and inflammatory biomarkers III
Description
Maternal levels of copeptin in serum
Time Frame
At gestational week 36-37
Title
Metabolic and inflammatory biomarkers IV
Description
Maternal levels of leptin in serum
Time Frame
At gestational week 36-37
Title
Metabolic and inflammatory biomarkers V
Description
Maternal levels of midregion pro-adrenomedullin (MR-proANP) in serum
Time Frame
At gestational week 36-37
Title
Maternal cardiometabolic risk profile
Description
A maternal cardiometabolic risk profile score one year post partum will be calculated using information on triglycerides and high-density cholesterol in serum, waist circumference, blood glucose as well as the systolic and diastolic blood pressure.
Time Frame
One year post partum
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
a confirmed diagnosis of GDM detected by oral glucose tolerance test in accordance with the World Health Organization guidelines
Exclusion Criteria:
known pre-pregnancy diabetes
twin pregnancy
<18 years of age
severe co-morbidities that would limit participation or a previously diagnosed severe psychiatric illness.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marie Löf, Professor
Phone
+46 734 426417
Email
marie.lof@ki.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marie Löf, Professor
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Maternity health care, Region Östergötland
City
Linköping
ZIP/Postal Code
58185
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Caroline Lilliecreutz, MD, Associate professor
12. IPD Sharing Statement
Plan to Share IPD
No
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SPARK- a Digital Platform to Improve Self-management of Gestational Diabetes
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