Effects of Exercise During Gestation on Maternal and Foetal Health (GESTAFIT)

September 30, 2019 updated by: Virginia A. Aparicio García-Molina, Universidad de Granada

Effects of Supervised Exercise During Gestation on Maternal and Foetal Health Markers. The GESTAFIT Project

The main objective of this project is to assess the effects of a novel and supervised exercise intervention in overweight pregnant and their newborn.

Methods/Design: The present study is a Randomized Controlled Trial. Sixty overweight pregnant interested in participate in the intervention program will be randomly assigned to either exercise (3 sessions/week), or to usual care (control) group (30 pregnant per group). The primary outcome measures are maternal weight gain, and maternal and neonatal glycaemic profile. Secondary outcomes measure are: i) body composition; ii) dietary patterns; iii) physical fitness; iv) objectively measured physical activity and sedentary behaviour; v) sleep quality; vi) mental health, quality of life and positive health; vii) haematology and biochemical analysis; viii) oxidative stress; ix) pro- and anti-inflammatory markers; x) bone health biomarkers; xi) adiposity-related proteins expression. The data will be analysed on an intention-to-treat basis and per protocol.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

140

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

      • Granada, Spain, 18071
        • Pilar Cabello-Turmo

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

25 years to 40 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Description

Inclusion criteria:

  • Overweight pregnant woman with a normal pregnancy course.
  • Answer "no" to all questions on the PARmed-X for pregnancy*.
  • To be able to walk without assistance.
  • To be able to read and write enough.
  • Informed consent: To be capable and willing to provide consent. *In addition, specific inclusion criteria for data analysis are: gestational age at delivery of 37-42 weeks with single foetus, spontaneous vaginal delivery or instrumental vaginal and caesarean without maternofoetal pathology (or other indication that does not involve maternofoetal risk, such as disproportion, failed induction, no foetal progression or non-cephalic presentation), newborn with appropriate weight, Apgar score>7 in the 1st and 5th minute of life, cord blood pH (normal>7.20) and normal monitoring results.

Exclusion criteria:

  • Acute or terminal illness.
  • Malnutrition.
  • Inability to conduct tests for assessing physical fitness or exercise during pregnancy.
  • Underweight, normal-weight or obesity.
  • Pregnancy risk factors (such as hypertension, type 2 diabetes, etc.).
  • Multiple pregnancies.
  • Chromosopathy or foetal malformations.
  • Uterine growth restriction.
  • Foetal death.
  • Upper or lower extremity fracture in the past 3 months.
  • Presence of neuromuscular disease or drugs affecting neuromuscular function
  • Be registered in other exercise program
  • Perform more than 300 minutes of at least moderate physical activity per week
  • Unwillingness to either complete the study requirements or to be randomised into control or intervention group.

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Single Group Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Exercise intervention
3 times per week from the 17th week of gestation until delivery
The exercise intervention will be performed in two groups so that each group will have 12-13 participants.The groups will train 3 days/week (60min per session) from the 16th week of gestation until delivery. The exercise intervention group will go through different phases of training: a) Learning phase: which will involve the intervention plan, the goals we want to work, and how we will perform it; b) Movement Learning phase: theoretical and practical sessions with the explanation of movements and ergonomic basic patterns; and c) Physical Fitness Training phase: with training sessions aimed at improving fitness and weight loss, and training sessions focused on a correct pelvic mobilization for the delivery.The intensity will be adapted during the exercise program based on the week of gestation and each pregnant heart rate. The sessions will consist of a mixed work, composed of circuits where both muscular and cardiovascular conditioning will be implemented.
No Intervention: Control group
Usual care (control) group

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Insulin sensitivity derived from the homeostatic model assessment for insulin resistance (HOMA-IR)
Time Frame: 34th week of gestation
Insulin sensitivity will be derived from the homeostatic model assessment for insulin resistance (HOMA-IR), which will be calculated using the formula [fasting insulin (μIU/mL) x fasting glucose (mg/dL)]/405.
34th week of gestation
Maternal weight gain (kg)
Time Frame: 34th week of gestation
Maternal weight gain will be defined as the weight change from baseline measurement to the last measurement
34th week of gestation
Neonatal insuline-glucose index
Time Frame: At delivery in cord blood samples
Neonatal insulin sensitivity will be assessed through the ratio glucose/insulin.
At delivery in cord blood samples

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Systolic and diastolic blood pressure (mmHg)
Time Frame: at the 16th and 34th week of gestation
Systolic and diastolic blood pressure (mmHg) will be measured after 5 minutes of rest, on 2 separate occasions (with 2 minutes between trials), with the person seated (Omron Health Care Europe B.V. Hoolddorp). The lowest value of the two trials will be selected for the analysis.
at the 16th and 34th week of gestation
Resting heart rate (bpm)
Time Frame: at the 16th and 34th week of gestation
Resting heart rate (bpm), will be measured after 5 minutes of rest, on 2 separate occasions (with 2 minutes between trials), with the person seated (Omron Health Care Europe B.V. Hoolddorp). The lowest value of the two trials will be selected for the analysis.
at the 16th and 34th week of gestation
The Mediterranean Diet Score
Time Frame: at the 16th and 34th week of gestation
The Mediterranean Diet Score in a version adapted to the specific needs during pregnancy for Fe, Ca and folic acid will be used to assess the adherence to the traditional Mediterranean dietary pattern.
at the 16th and 34th week of gestation
Cardiorespiratory fitness (Vo2max)
Time Frame: at the 16th and 34th week of gestation
The modified Bruce protocol will be performed to estimate maximal oxygen uptake (VO2max), and will be used as measure of cardiorespiratory fitness.
at the 16th and 34th week of gestation
Cardiorespiratory fitness (meters in the 6-min walk test)
Time Frame: at the 16th and 34th week of gestation
We perform the 6-minute walk test, which measures the maximum distance (in meters) each participant can walk in 6 minutes along a 45.7 m rectangular course.
at the 16th and 34th week of gestation
Muscle strength (kg)
Time Frame: at the 16th and 34th week of gestation
The handgrip strength test will be used as measure of strength
at the 16th and 34th week of gestation
Flexibility (cm)
Time Frame: at the 16th and 34th week of gestation
The back-scratch test will be used as measure of flexibility
at the 16th and 34th week of gestation
Physical activity and sedentary behaviour (in minutes)
Time Frame: at the 16th, 24th and 34th week of gestation
Accelerometry will be used to objectively assess physical activity and sedentary time. Women will be asked to wear a tri-axial accelerometer (ActiSleep+, Pensacola, Florida, United States) for 9 consecutive days, starting the same day they receive the monitor (e.g. participants who receive the accelerometer on Monday, will carry the device until Tuesday of the next week). Participants will be instructed to wear the accelerometer during the whole day (24 hours) on their wrist attached by an elastic belt. Time (in minutes) engaged in light, moderate, and moderate-vigorous intensity PA and sedentary time will be calculated. This accelerometer has been previously used in pregnancy with similar methodology as described in the present protocol.
at the 16th, 24th and 34th week of gestation
Sleep behaviours (through accelerometry)
Time Frame: at the 16th, 24th and 34th week of gestation
Behaviours related to sleep, such as sleep onset, sleep latency, total sleep time, number and duration of awakenings and sleep efficiency will be objectively calculated by using a triaxial accelerometer (ActiSleep+, Pensacola, Florida, United States). The data analysis of such ActiSleep accelerometry data will be carried out through its specific software (Actilife).
at the 16th, 24th and 34th week of gestation
Pittsburgh Sleep Quality Index
Time Frame: at the 16th, 24th and 34th week of gestation
It will be used to assess sleep quality and disturbances over a l-month time interval.
at the 16th, 24th and 34th week of gestation
Insomnia Symptoms Questionnaire
Time Frame: at the 16th, 24th and 34th week of gestation
The presence of symptoms of insomnia will be measured with the Insomnia Symptoms Questionnaire, validated in pregnant women.
at the 16th, 24th and 34th week of gestation
Quality of life (Short-Form Health Survey 36)
Time Frame: at the 16th and 34th week of gestation
We will use the Short-Form Health Survey 36, for assessing health-related quality of life.
at the 16th and 34th week of gestation
Epidemiological Studies-Depression Scale questionnaire
Time Frame: at the 16th and 34th week of gestation
The pregnant antenatal depression levels will be assessed by the Center for Epidemiological Studies-Depression Scale questionnaire, which is validated and widely employed in pregnancy.
at the 16th and 34th week of gestation
State Trait Anxiety Index.
Time Frame: at the 16th and 34th week of gestation
Anxiety levels will be assessed with the State Trait Anxiety Index.
at the 16th and 34th week of gestation
The Detention of Restless Legs Syndrome questionnaire
Time Frame: at the 16th and 34th week of gestation
The "Restless Legs Syndrome" largely determines the quality of life for many pregnant and is related to their levels of depression and sleep quality. The Spanish version of the Detention of Restless Legs Syndrome questionnaire will be employed to assess the presence and severity of this syndrome .
at the 16th and 34th week of gestation
Oswestry Disability Index score
Time Frame: at the 16th and 34th week of gestation
Low-back pain will be assessed with the Spanish version of the Oswestry Disability Index score
at the 16th and 34th week of gestation
Pain Visual Analogue Scale
Time Frame: at the 16th and 34th week of gestation
Low-back pain intensity will be also assessed with the Pain Visual Analogue Scale
at the 16th and 34th week of gestation
6-item Female Sexual Function Index
Time Frame: at the 16th and 34th week of gestation
The 6-item Female Sexual Function Index will be used to assess sex function. This instrument is composed of six questions: desire, arousal, lubrication, orgasm, satisfaction and pain. Each question can be scored from 0 to 5 and then summed up to provide a total score.
at the 16th and 34th week of gestation
Positive health
Time Frame: at the 16th and 34th week of gestation

"Positive health" will be evaluated through the following questionnaires:

  1. The Trait Meta-Mood Scale
  2. The Positive and Negative Affect Schedule
  3. The Satisfaction with Life Scale
  4. The 10-item Connor-Davidson Resilience Scale
at the 16th and 34th week of gestation
Haematology
Time Frame: at 34th week of gestation and at delivery
Erythrocyte count, haematocrit, haemoglobin, platelets, leukocytes and erythrocyte mean corpuscular volume will be quantified by Coulter (Brand).
at 34th week of gestation and at delivery
Lipid profile (in mother and cord blood)
Time Frame: at 34th week of gestation and at delivery
Plasma total, high-density lipoprotein and low-density lipoprotein cholesterol and triglycerides (all in mg/dL) will be assessed using an autoanalyzer (Hitachi-Roche p800, F. Hoffmann-La Roche Ltd. Switzerland)
at 34th week of gestation and at delivery
Glycaemic profile (in mother and cord blood)
Time Frame: at 34th week of gestation and at delivery
Plasma glucose, insulin and glycosylated haemoglobinwill be assessed using an autoanalyzer (Hitachi-Roche p800, F. Hoffmann-La Roche Ltd. Switzerland)
at 34th week of gestation and at delivery
Total plasma antioxidant capacity (in mother and cord blood)
Time Frame: at 34th week of gestation and at delivery
It will be measured by using commercial kit (spectrophotometry).
at 34th week of gestation and at delivery
Plasma liposoluble antioxidants (in mother and cord blood)
Time Frame: at 34th week of gestation and at delivery
Plasma vitamin E, retinol, carotene, coenzyme Q10 and coenzyme Q9 will be measured through mass spectrometry
at 34th week of gestation and at delivery
Antioxidant enzymes activity (in mother and cord blood)
Time Frame: at 34th week of gestation and at delivery
Eritrocite membrane catalase, glutathione peroxidase and superoxide dismutase enzymes will be by measured by spectrophotometry.
at 34th week of gestation and at delivery
Carbonyl proteins (in mother and cord blood)
Time Frame: at 34th week of gestation and at delivery
Measurement of carbonyl proteins will be done by using commercial kit (spectrophotometry).
at 34th week of gestation and at delivery
Oxidative damage to lipids (in mother and cord blood)
Time Frame: at 34th week of gestation and at delivery
Measurement of 4-hydroxynonenal and isoprostanes in urine and plasma and hydroperoxides in plasma and erythrocyte membrane by using commercial kits (spectrophotometry and ELISA)
at 34th week of gestation and at delivery
Oxidative damage to DNA (in mother and cord blood)
Time Frame: at 34th week of gestation and at delivery
measurement of 8-hydroxyguanosine in urine and plasma by commercial kits (ELISA).
at 34th week of gestation and at delivery
Pro- and anti-inflammatory signal (in mother and cord blood)
Time Frame: at 34th week of gestation and at delivery
Some maternal and umbilical cord plasma pro-inflammatory and anti-inflammatory cytokines (IL-1β, IL-2, IL-6, IL-8, IL-10, IFN-γ and TNF-α, IL-1ra and TNF Srii α), some adipokines (adiponectin, adipsin, resistin, PAI-active, insulin and leptin) and myokines (irisin) will be measured by the employment of Luminex xMAP technology.
at 34th week of gestation and at delivery
Bone biomarkers (in mother and cord blood)
Time Frame: at 34th week of gestation and at delivery
Various relevant biomarkers related to bone metabolism (ACTH, DKK-1, FGF-23, Osteocalcin, OPN-Osteopontin, Osteoprotegerin, PTH and SOST) will be measured with Luminex xMAP technology.
at 34th week of gestation and at delivery
Adiposity-related proteins expression (in mother and cord blood)
Time Frame: At delivery

Glucocorticoid receptor; peroxisome proliferation activated receptor (PPAR); the beta-11 hydroxysteroid dehydrogenase type I (11βHSD1), and beta-11 hydroxysteroid dehydrogenase type II (11βHSD2) will be assessed in maternal and umbilical cord blood and in oral mucosa from the mother and newborn.

Moreover, 4 genes highly involved in foetal and postnatal development of adipose tissue have been selected; two are receptors: the Glucocorticoid receptor and the PPAR-γ, and two are metabolic enzymes: beta-11 hydroxysteroid dehydrogenase type I or 11βHSD1, and 11 beta-hydroxysteroid dehydrogenase type II or 11βHSD2. Of great importance are PPAR-γ1 and PPAR-γ2, which are generated from the same gene by alternative promoter usage and mRNA. We will measure such proteins as well as paraoxonase/arylesterase 1 (PON1) concentrations in maternal and umbilical cord plasma by Polymerase Chain Reaction and Western Blot techniques.

At delivery

Collaborators and Investigators

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Publications and helpful links

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General Publications

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 (Actual)

October 1, 2015

Primary Completion (Actual)

July 1, 2017

Study Completion (Actual)

July 1, 2018

Study Registration Dates

First Submitted

October 6, 2015

First Submitted That Met QC Criteria

October 19, 2015

First Posted (Estimate)

October 21, 2015

Study Record Updates

Last Update Posted (Actual)

October 1, 2019

Last Update Submitted That Met QC Criteria

September 30, 2019

Last Verified

September 1, 2019

More Information

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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