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Completed

NCT Number: NCT02931656

Acute Effects of an Aquatic Physical Exercise on Glycemic Control of Gestational Diabetes

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.

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Key information

Age range

18 year–35 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

José Roberto da Silva Junior

Recife, Pernambuco, 50070-550, Brazil

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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;

Treatment and study plan

Aquatic Exercise

Other

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: Water aerobics, Hydrotherapy

Primary outcomes

  1. Change from Glycemic level

    Time frame: Before and up to 5 minutes after the intervention

    Blood glucose test: maternal glucose levels

Secondary outcomes

  1. Change from Systolic and diastolic blood pressure

    Time frame: Before and up to 5 minutes after the intervention

    Measured in mmHg every medical consultation

  2. Change from Heart rate (pulse)

    Time frame: Before and up to 5 minutes after the intervention

    number of beats in 60 seconds

  3. Change from Respiratory rate

    Time frame: Before and up to 5 minutes after the intervention

    number of movements indicative of inspiration and expiration per 60 seconds

  4. Change from Oxygen saturation

    Time frame: Before and up to 5 minutes after the intervention

    Quantity oxygen is being transported in the blood at the time of measurement

  5. Change from Fetal heart rate

    Time frame: Before and up to 5 minutes after the intervention

    Heartbeat frequency of the fetus per minute

Sponsors and collaborators

Lead sponsor

Professor Fernando Figueira Integral Medicine Institute

Other

Collaborators

  • Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.
  • Fundação de Amparo à Ciência e Tecnologia de Pernambuco

Registry information

Important dates

Study start
2016
Primary completion
2018
Study completion
2019
First posted
Oct 13, 2016
Registry last updated
Oct 9, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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