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Interval Walking Intervention for Pregnant Women Diagnosed With Gestational Diabetes Mellitus

Primary Purpose

Gestational Diabetes Mellitus in Pregnancy

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
IWT-group
Sponsored by
The Danish Center for Strategic Research on Type 2 Diabetes
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Gestational Diabetes Mellitus in Pregnancy

Eligibility Criteria

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

Inclusion Criteria:

  • Diagnosed with GDM by a 2 hour oral glucose tolerance test with a BG level of >9.00mmol/l at 2 hours
  • Danish speaking
  • >18 years of age
  • Live <20 kilometers from Odense city center

Exclusion Criteria:

  • Pelvic pains
  • Untreated depression
  • Walking disabilities
  • Pregnancy-related complications
  • >32 weeks

Sites / Locations

  • Danish Centre of strategic research of type 2 diabetes

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

IWT-group

Con-group

Arm Description

The IWT-group follows the standardized GDM care program for GDM patients at OUH and is prescribed to a 6-week non-supervised IWT-program consisting of 3 IWT sessions per week of 40-50 minutes each.

The con-group follows the standardized GDM care program for GDM patients at OUH

Outcomes

Primary Outcome Measures

Compliance to the prescribed IWT-intervention
Compliance defined as adherence to the prescribed IWT-intervention
Compliance to the prescribed IWT-intervention
Compliance defined as the quality of the the IWT sessions

Secondary Outcome Measures

Glycemic control
Blood glucose variations measured by 48-hour continuous glucose monitoring
Physical activity level
Physical activity level measured by accelerometers
Physical fitness
Physical fitness measured by the on-board fitness test in the InterWalk application and a 6-minute walking test

Full Information

First Posted
June 28, 2017
Last Updated
July 24, 2018
Sponsor
The Danish Center for Strategic Research on Type 2 Diabetes
Collaborators
Odense University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03229161
Brief Title
Interval Walking Intervention for Pregnant Women Diagnosed With Gestational Diabetes Mellitus
Official Title
Interval Walking Intervention for Pregnant Women Diagnosed With Gestational Diabetes Mellitus - a Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
January 3, 2017 (Actual)
Primary Completion Date
May 31, 2017 (Actual)
Study Completion Date
May 1, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Danish Center for Strategic Research on Type 2 Diabetes
Collaborators
Odense University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
It is well-known that regular physical activity (PA) can improve glycemic control and physical fitness in type 2 diabetes patients. However, studies examining the effects of PA in patients with gestational diabetes mellitus (GDM) are limited. Interval walking training (IWT) is a careful type of PA consisting of repeatedly cycles of 3 min. fast and slow walking. The investigators aimed to examine, if IWT is feasible as PA intervention for GDM patients, and to examine the effects of IWT on glycemic control, PA levels and physical fitness.
Detailed Description
Gestational diabetes mellitus (GDM), defined as glucose intolerance and thus hyperglycemia with onset or first recognition during pregnancy, is steadily increasing in prevalence. In Denmark, the prevalence of GDM is around 2-3% of all pregnancies. GDM is associated with several adverse perinatal and maternal outcomes why early recognition and diagnosis is important. Early diagnosis and relevant treatment can prevent adverse outcomes of the baby and mother, such as macrosomia, shoulder dystocia, preeclampsia and hypoglycemia. The glucose levels will often normalize shortly after birth; however, up to 50% of all women in Denmark diagnosed with GDM develop T2D during the first 10 years after the pregnancy, have a threefold risk of developing metabolic syndrome2 10, while the recurrence risk of developing GDM in subsequent pregnancies varies between 30-84%. Furthermore, long term increased risks for children born with macrosomia or by a mother with GDM include cardiovascular disease, obesity and T2D. Glycemic control is a key factor in combatting the severe effects related to poorly controlled GDM. Management of GDM in Denmark consists of regular BG self-monitoring, dietary modifications, and in some cases insulin treatment. Additionally, obstetric control visits and PA advices are also a part of the standard GDM care program. Compared to non-pregnant women, pregnant women must be more careful in relation to especially the type of PA, why supervised exercise is often recommended in order to ensure safe and correct guidance. This is a heavy economic burden, why a structured, non-supervised type of PA with low a risk of injury, possibly high compliance and continuous monitoring would be preferable. Interval walking training (IWT) is a lenient type of structured, non-supervised PA. This type of PA is associated with an improved glucose regulation in patients with T2D after 4 months of IWT 5 times weekly (60 min./session) (Karstoft et al., 2013). Due to similar metabolic dysregulations in patients with T2D and GDM, the investigators are apt to believe that IWT, if feasible, can improve glycemic control in GDM patients. Furthermore, it is obvious to believe that IWT can be implemented as regular PA in GDM patients, as one study has shown that pregnant women mostly prefer walking as a type of PA during pregnancy. This open-label randomized controlled trial aims to enroll 20 patients randomized (1:1) to a control- (Con) or IWT-group. Both groups will follow the standard GDM care program at Odense University Hospital. Additionally, the IWT-group is prescribed three weekly IWT sessions of 40-50 minutes each for 6 weeks. Each IWT session is guided and controlled by the smartphone application 'InterWalk', which individualize the training intensity to current fitness level of the patient through an on-board fitness test.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This open-label randomized controlled trial aims to enroll 20 patients randomized (1:1) to a control- (Con) or IWT-group. Patients in both the IWT- and Con-group follows the standardized GDM care program for GDM patients at OUH through the 6-week intervention period, which consists of instruction of self-monitoring of BG levels, dietary guidance, and in some cases, insulin treatment. Additionally, the program also consists of close obstetric control visits and exercise guidance. All patients are instructed not to start any new type of PA after inclusion and continue their lives without any changes. Patients randomized to the IWT-group goes through a 6-week non-supervised IWT-program, where they are prescribed to conduct 3 IWT sessions per week of 40-50 minutes each. Before and after the 6-week intervention, maternal blood glucose (BG) levels is measured by continuous glucose monitoring, PA level measured using accelerometers and physical fitness measured using two walking tests.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
3 (Actual)

8. Arms, Groups, and Interventions

Arm Title
IWT-group
Arm Type
Experimental
Arm Description
The IWT-group follows the standardized GDM care program for GDM patients at OUH and is prescribed to a 6-week non-supervised IWT-program consisting of 3 IWT sessions per week of 40-50 minutes each.
Arm Title
Con-group
Arm Type
No Intervention
Arm Description
The con-group follows the standardized GDM care program for GDM patients at OUH
Intervention Type
Behavioral
Intervention Name(s)
IWT-group
Primary Outcome Measure Information:
Title
Compliance to the prescribed IWT-intervention
Description
Compliance defined as adherence to the prescribed IWT-intervention
Time Frame
After the 6-week intervention period
Title
Compliance to the prescribed IWT-intervention
Description
Compliance defined as the quality of the the IWT sessions
Time Frame
After the 6-week intervention period
Secondary Outcome Measure Information:
Title
Glycemic control
Description
Blood glucose variations measured by 48-hour continuous glucose monitoring
Time Frame
Before and after the 6-week intervention period
Title
Physical activity level
Description
Physical activity level measured by accelerometers
Time Frame
7 days before and after the 6-week intervention period, and the first and last 5 days during the 6-week intervention period
Title
Physical fitness
Description
Physical fitness measured by the on-board fitness test in the InterWalk application and a 6-minute walking test
Time Frame
Before and after the 6-week intervention period
Other Pre-specified Outcome Measures:
Title
Blood pressure
Description
30 minutes systolic and diastolic Blood Pressure (BP) together with pulse wave velocity (PWV) was measured by using the Mobil-O Graph® PWA device. BP and PWV was measured every 3 minutes for 30 minutes in a sitting position with the assessor only being in the room during the first measurement to ensure adequate quality.
Time Frame
Before and after the 6-week intervention period
Title
Physical and mental health
Description
Perceived physical and mental health was measured using the SF-12 questionnaire.
Time Frame
Before and after the 6-week intervention period
Title
BMI
Description
Body height and body weight were objectively measured. Height was measured in an upright standing position without shoes by using a stadiometer. Weight was also measured in a standing position without shoes by using a digital scale. Height and weight was measured to the nearest 0.5 centimeter and 0.1 kilo respectively. BMI was calculated based on measured height and weight
Time Frame
Before and after the 6-week intervention period

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
As only women can be diagnosed with gestational diabetes mellitus, only women are eligible in participating in the study.
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosed with GDM by a 2 hour oral glucose tolerance test with a BG level of >9.00mmol/l at 2 hours Danish speaking >18 years of age Live <20 kilometers from Odense city center Exclusion Criteria: Pelvic pains Untreated depression Walking disabilities Pregnancy-related complications >32 weeks
Facility Information:
Facility Name
Danish Centre of strategic research of type 2 diabetes
City
Odense
ZIP/Postal Code
5000
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Interval Walking Intervention for Pregnant Women Diagnosed With Gestational Diabetes Mellitus

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