- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02931656
Acute Effects of an Aquatic Physical Exercise on Glycemic Control of Gestational Diabetes
October 8, 2019 updated by: José Roberto da Silva Junior, Professor Fernando Figueira Integral Medicine Institute
Gestational diabetes mellitus (GDM) is increasing worldwide and has been associated with adverse perinatal outcomes and high risk for chronic disease both for the mother and for the child.
Physical exercise is feasible to diabetic pregnant women and contributes to a better glycemic control and to decrease adverse perinatal outcomes.
However there are no studies assessing the effects of aquatic physical exercise on GDM control.
Study Overview
Detailed Description
The study will be conducted at Institute of Medicine Professor Fernando Figueira (IMIP), Brazil.
The patients will be included in the study by consent after an explanation of the study goals.
Women will be considered eligible for enrollment if they fulfill all the inclusion criteria and none of the exclusion criteria.
Sample size was calculated with the aim of reducing glucose levels by 20% in intervention GDM group.
A power of 80% and a level of significance of 5% was accepted and the calculated sample size in each arm was 30 patients.
Assuming a drop out of 20%, 72 pregnant women will be included in the study.
36 gestational diabetics and and 36 normoglycemic pregnant women will develop an aquatic physical exercise in a thermal pool, 45 minutes per one time, from rehabilitation center of the IMIP.
Before to practice the aquatic exercise women will have their physical capacity assessed by the Six minutes walk test and fetal conditions will be assessed by ultrasound.
They will also be submitted to a dermatological examination by specialist.
Primary endpoint will be glucose levels (glycemic test), secondary endpoints will be the following maternal and fetal: blood pressure, heart rate, respiratory rate, oxygen saturation level, fetal cardio beat and fetal movement.The variables will be measured before and after the water exercise session.
Maternal and fetal characteristics of the study sample will be presented by group, intervention and control in terms of mean and standard deviation.
For group comparisons of glucose levels and maternal and fetal variables, continuous and nominal data will be analyzed by t test for unpaired data and χ2 tests, respectively.
Data will be analyzed using the intention-to-treat principle.
Statistical analysis will be performed with the STATA version 12.0 and the level of significance will set to <0.05.
Even in cases where there is the appearance of some criterion for discontinuation during the intervention (Aquatic physical exercise), the patient will be considered part of the group which was initially included in the randomization (intent to treat) and is not excluded from the study.
The physical proprieties of water provide aquatic exercises as ideal for pregnant women.
An aquatic physical exercise program developed with pregnant women in a thermal pool and under a physiotherapist supervision must ensure compliance.
It is expected that this study provide evidences to the real role of aquatic physical exercise on glycemic control of GDM.
Study Type
Interventional
Enrollment (Actual)
70
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Pernambuco
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Recife, Pernambuco, Brazil, 50070-550
- José Roberto da Silva Junior
-
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 35 years (ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- GDM Group: GDM diagnosis will be based on International Association of the Diabetes in Pregnancy Study Group (IADPSG) and WHO, Hyperglycemia and Adverse Pregnancy Outcomes (HAPO) study (2 h 75 g oral glucose tolerance test (OGTT): a fasting glucose ≥ 92 mg/dl or a one hour result of ≥ 80 mg/dl, or a two hour result of ≥ 153 mg/dl;
- Control Group: Normal glucose tolerance (IADPSG /WHO)
- Aging 18 to 35 years;
- Physically inactive (< 150' per week based on International Physical Activity Questionnaire.
Exclusion Criteria:
- Kidney disease or collagenosis;
- Previous history of gestational diabetes;
- Diabetes type 1 or type 2;
- Hypertensive disorders related to pregnancy;
- Hemodynamic instability;
- Obstetric labor;
- Vaginal bleeding;
- Cognitive disorder, auditory, visual or motor severely limiting, attested by a medical specialist;
- Skin disorders who have a contraindication to the use of a swimming pool;
- Urinary tract infection;
- Be inserted in the program of regular exercise;
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: NON_RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: GDM aquatic exercise
GDM Diagnosis criteria accordance with to IADPSG / WHO
|
The aquatic exercise program will be under the professional guidance of a physiotherapist, with water at a temperature of around 26 to 28°C.
The exercise sessions will be executed following the steps: 1) Heating (stretching and flexibility, static method, during 5'); 2) Aerobic exercise (running, displacements and combined movements of arms and legs, with 1minute interval, to 1minute activity and of during 20') 3) Spot exercises (strength / endurance of the upper and lower limbs and abdomen, using the resistance of water for 15') 4) Relaxation (slow walks for 5').
During the sessions of exercises the pregnant women will have heart rate monitored by the frequency meter (Polar Electro OY) to control the intensity of the exercises that will focus on the range of moderate intensity.
Other Names:
|
ACTIVE_COMPARATOR: Control Group aquatic exercise
No change in blood glucose levels Group, investigated between 24-28 weeks of gestation.
|
The aquatic exercise program will be under the professional guidance of a physiotherapist, with water at a temperature of around 26 to 28°C.
The exercise sessions will be executed following the steps: 1) Heating (stretching and flexibility, static method, during 5'); 2) Aerobic exercise (running, displacements and combined movements of arms and legs, with 1minute interval, to 1minute activity and of during 20') 3) Spot exercises (strength / endurance of the upper and lower limbs and abdomen, using the resistance of water for 15') 4) Relaxation (slow walks for 5').
During the sessions of exercises the pregnant women will have heart rate monitored by the frequency meter (Polar Electro OY) to control the intensity of the exercises that will focus on the range of moderate intensity.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change from Glycemic level
Time Frame: Before and up to 5 minutes after the intervention
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Blood glucose test: maternal glucose levels
|
Before and up to 5 minutes after the intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change from Systolic and diastolic blood pressure
Time Frame: Before and up to 5 minutes after the intervention
|
Measured in mmHg every medical consultation
|
Before and up to 5 minutes after the intervention
|
Change from Heart rate (pulse)
Time Frame: Before and up to 5 minutes after the intervention
|
number of beats in 60 seconds
|
Before and up to 5 minutes after the intervention
|
Change from Respiratory rate
Time Frame: Before and up to 5 minutes after the intervention
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number of movements indicative of inspiration and expiration per 60 seconds
|
Before and up to 5 minutes after the intervention
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Change from Oxygen saturation
Time Frame: Before and up to 5 minutes after the intervention
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Quantity oxygen is being transported in the blood at the time of measurement
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Before and up to 5 minutes after the intervention
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Change from Fetal heart rate
Time Frame: Before and up to 5 minutes after the intervention
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Heartbeat frequency of the fetus per minute
|
Before and up to 5 minutes after the intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Study Director: João Guilherme Bezerra Alves/, Doctor, Institute of Integrative Medicine Professor Fernando Figueira
- Study Chair: Alex Sandro Rolland de Souza, Doctor, Institute of Integrative Medicine Professor Fernando Figueira
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2016
Primary Completion (ACTUAL)
December 1, 2018
Study Completion (ACTUAL)
June 1, 2019
Study Registration Dates
First Submitted
September 28, 2016
First Submitted That Met QC Criteria
October 11, 2016
First Posted (ESTIMATE)
October 13, 2016
Study Record Updates
Last Update Posted (ACTUAL)
October 9, 2019
Last Update Submitted That Met QC Criteria
October 8, 2019
Last Verified
October 1, 2019
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1111-1188-1100
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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