MedPath

Structured Aerobic and Resistance Exercise and Gestational Diabetes

Not Applicable
Completed
Conditions
Gestational Diabetes Mellitus
Interventions
Other: Structured Exercise
Registration Number
NCT02196571
Lead Sponsor
Association for Functional Rehabilitation, Recreation and Applied Kinesiology Impulse
Brief Summary

Gestational diabetes mellitus (GDM) is defined as impaired glucose tolerance of various degrees first manifested during pregnancy. The primary aim of treating GDM is to optimize glycaemic control and improve pregnancy outcomes. Also, as part of treatment, it is recommended to continue or initiate exercising with moderate intensity. However, available data on the effects of physical activity on GDM are based on a small number of trials. The aim of the trial is to examine and add new scientific evidence on possible health-related effects of application of structured programme consisting of aerobic and resistance exercises on the course and outcomes of GDM. Primary goal of research is to determine how proposed exercise programme effects glycaemic control, rate of complications during pregnancy, labour, delivery, immediate after delivery and health status of newborn. Main hypothesis is that parameters of glycaemic control, course of GDM, complications during delivery and birth outcomes directly and significantly correlate with participation in structured programme of exercise. Research will be conducted as experimentally designed randomized controlled trial. Participants will be pregnant women diagnosed with GDM, age between 20 and 40, without comorbidities. Women in the experimental group will be included in exercise programme two times per week with duration of 50 minutes. Training sessions will start right after the diagnosis and will be performed until the end of the pregnancy. The training protocol will follow international guidelines (ACOG, 2001; ACOG, 2002; ADA, 2008; NICE, 2008; ADA 2011). Women in the control group will receive standard medical care.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
42
Inclusion Criteria
  • established diagnosis of gestational diabetes,
  • age between 20 and 40,
  • otherwise healthy pregnancy
Exclusion Criteria
  • pharmacological treatment with oral hypoglicemics and/or insulin therapy introduced prior to trial enrollment,
  • existing comorbidities and
  • contraindications for exercise

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Exercise and lifestyle changeStructured ExerciseWomen in the experimental group will be included in structured exercise programme two times per week with duration of 50 minutes.Participants will start with training sessions right after they are diagnosed with GDM and they will exercise until the end of the pregnancy or occurence of contraindications. Programme will consist of aerobic exercises (20 minutes), resistance exercises (20 minutes), plevic floor, stretching and relaxation exercises (10 minutes). Women in control group will receive standard antenatal care.
Primary Outcome Measures
NameTimeMethod
Number of pregnant women with complications during pregnancy, labour and deliveryup to labour

Blood glucose levels, need for insulin and oral hypoglycemic drugs, need for cesarean section and other operative delivery methods, other adverse occurences during pregnancy, labour and delivery

Secondary Outcome Measures
NameTimeMethod
Weight gain in pregnancyAfter recruitment and during pregnancy (30, 33 and 36 weeks)

Body mass and percentage of fat measured by caliper

Number of macrosomic infantsdelivery

Trial Locations

Locations (1)

Association for functional rehabilitation, recreation and applied kinesiology Impuls

🇭🇷

Zagreb, Croatia

© Copyright 2025. All Rights Reserved by MedPath