Active Pregnancy. Mental and Emotional Health Care to Pregnant Woman During and After Coronavirus (COVID-19) (GESTACTIVE)

June 28, 2022 updated by: Rubén Barakat Carballo, Universidad Politecnica de Madrid

Active Pregnancy. Mental and Emotional Health Care to Pregnant Woman During and After COVID-19

The complex process of pregnancy and childbirth can determine the future health of mother and child. It is the only vital process that involves the modification of practically all of a woman's body systems in order to sustain fetal life. In this sense, it is essential to ensure adequate functioning of all maternal physiological, mental and emotional mechanisms that facilitate fetal growth and development. Complications in any of these health domains and functions may contribute to pathologies and complications that have a detrimental impact on maternal and newborn health.

Pregnancy could be a vulnerable period for women, especially regarding mental and emotional illnesses, which are more likely to manifest during this time compared to other periods of their life. In this sense, a high prevalence of prenatal stress, anxiety and depression exists, which are associated with downstream newborn complications as well.

Depressive symptoms such as sadness, decreased interest in everyday activities, reduced energy and concentration are generated by the aforementioned gestational lability, these symptoms would appear (mostly) at the beginning of the pregnancy. Feelings of being overwhelmed, uneasiness, threat or imminent danger, uncertainty, difficulty in making decisions, obsessive thoughts could be caused by prenatal anxiety.

According to scientific literature, the consequences of mental and emotional disturbances during pregnancy go beyond the gestational period and affect mother, fetus, newborn, and even child development, including complications such as preterm delivery, prolonged and more instrumental labor, low birth weight, pre-term birth, infant's physical and cognitive developmental delay, and the poor mother-infant relationship.

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

COVID-19. Risks associated with an inactive pregnancy:

The impact of COVID-19 has generated a global crisis never before experienced, which affects physiological, emotional, mental, and social factors for all population groups, including those who are pregnant with important related risks.

The complications associated with confinement (no group support, reduced mobility, the distance between people, etc.), significantly affects the lifestyle of pregnant individuals and potentially remove one of the basic recommendations established by the international scientific community: a physically active lifestyle.

Scientific evidence confirms that engaging in an unhealthy lifestyle during pregnancy, including inactivity, enhances the risk of chronic disease for both mother and fetus. In fact, the growing epidemic of sedentary behavior affects pregnancy and childbirth with adverse pre, peri, and postnatal outcomes. Unfortunately, the situation caused by COVID-19 could further exacerbate sedentary behavior and its associated complications for pregnant women.

Current Status:

Before the COVID-19 pandemic, the range of prenatal mental and emotional alterations was close to 15-30%, the prevalence being particularly high in low- and middle-income countries. However, the new social and economic situation generated by the COVID-19 pandemic has raised these values significantly, in this sense 37% reported clinically relevant symptoms of depression and 57% of pregnant women experienced symptoms of anxiety.

This means that the pandemic has negatively affected the mental and emotional health of pregnant women, and consequently of future generations. It is necessary (urgent) to intervene right now with preventive policies and alternatives.

The difficulty and associated (maternal/fetal) risks of pharmacological treatment of mental and emotional illnesses during pregnancy, requires the scientific search for new alternatives, especially aimed at the prevention of these pathologies.

There are important lifestyle recommendations promoted by the scientific community about establishing elements that ensure a healthy pregnancy. However, a small percentage of pregnant women meet global healthy lifestyle guidelines. In fact, the scientific literature reports an increase of perinatal disorders, for example, a high percentage of women continue to gain excessive weight during pregnancy in spite of mentioned health recommendations, and this in turn also increases the risk for other complications.

There are no official estimates of healthcare costs that these complications generate but obviously, we speculate significant amounts.

Worldwide, 80% of pregnant women or (or maybe more) don´t achieve the minimum weekly amount of 150 minutes of moderate physical activity intensity. In Spain, this inactivity is similar to other countries, with approximately 19.7% of women achieving the American College of Obstetricians and Gynecologists (ACOG) recommendations to be active weekly during pregnancy.

Physical exercise as a preventive factor:

Given this complex problem, it is necessary (urgent) to find non-invasive prevention mechanisms to benefit the wellbeing of the mother and her child, taking into account that pregnancy predisposes the woman to a significant change in lifestyle.

As substantiated by scientific evidence, physical exercise during pregnancy does not cause adverse effects on the mother and fetus. Indeed, physical exercise during pregnancy may prevent chronic disease risk in the mother and fetus.

Although the scientific literature is not entirely conclusive, many studies show the positive influence of a physical activity program during pregnancy on maternal mental and emotional status (even with better benefits if it´s supervised); this could be a good approach to maintain healthy mental wellbeing.

GESTACTIVE will examine the effects of a supervised moderate exercise program during pregnancy as a preventive tool for mental and emotional distress, as well as associated complications. The results of this proposal will contribute to the improvement of the quality of life of pregnant women and thus the promotion of health of future generations.

Hypothesis Aerobic, moderate, and supervised exercise during pregnancy can be an efficient element of the prevention of mental and emotional alterations that the situation generated by COVID-19 causes to the healthy pregnant population and their children.

Objective Examine the influence of a supervised aerobic exercise program during pregnancy, in non-face-to-face and face-to-face ways, on the prevention of maternal mental and emotional health, fetal, newborn, and infant outcomes during the pandemic state and in the near future.

Material and Methods:

- Study design. A randomized clinical trial (RCT) will be carried out, not masked with healthy pregnant women, giving rise to two study groups: exercise group (EG), pregnant women participating in a regular program of supervised physical exercise and control group ( CG), pregnant women who receive normal obstetric monitoring of their pregnancy, including recommendations regarding dietary-nutritional factors, as well as the benefits of an active pregnancy. All selected pregnant women will sign an Informed Consent before participating in the study.

Women randomly assigned to the CG received general advice from their health care provider about the positive effects of physical activity. Participants in the CG had their usual visits with health care providers during pregnancy, which were equal to the exercise group. Women were not discouraged from exercising on their own. However, women in the CG were asked about their exercise once each trimester using a "Decision Algorithm" (by telephone).

Intervention

General characteristics of the physical exercise program:

  • The minimum adherence required will be 80% of the total sessions.
  • Onset: gestational week 9-11, immediately after the first prenatal ultrasound, in order to rule out Obstetric Contraindications for physical exercise.
  • End: gestational week 38-39.
  • Frequency: 3 weekly sessions, various possibilities will be offered at different times from which the pregnant woman can choose, in order to promote work and family conciliation.

Basic Considerations:

a, All the activities carried out will be aerobic.

b. Avoid working positions in which areas normally overloaded by pregnancy are further affected.

c. The work corresponding to flexibility will be carried out always bearing in mind that these are pregnant women, this forces us once again not to include forced operating positions in the exercises or to excessively maintain the stretching times in each area.

d. An adequate fluid intake will be maintained before and after the activity.

e. Also as a general rule and to eliminate potential risks, the following will be avoided:

  • Activities that include the Valsalva maneuver.
  • High ambient temperatures or very humid environments in order to avoid hyperthermia (body temperature higher than 38º C).
  • Sudden movements.
  • Positions of extreme muscular tension.

Structure:

All sessions will begin with a warm-up of 7-8 minutes composed of mild movements and joint mobility of upper and lower limbs exercises. Then a central part of 35-40 minutes, four types of activities will be included (aerobic work, muscle strengthening, coordination/balance tasks, pelvic floor exercises), finally a section of flexibility, relaxation and final talk (comments and sharing) will be performed (12-15 minutes).

Below we offer a greater detail of each part:

I. Warm-up-General activation. Displacements varied without impact activities (avoiding jumps, falls). Mild work of mobility of the main joints.

II. Aerobic section. Exercise to increase intensity up to moderate activities, play with sports equipment (balls, ropes, pikes), or choreographies of different musical styles.

III. Muscle strengthening, general toning exercises of the whole body: lower part (calf, quadriceps, hamstrings, adductors, abductors), upper part (abdominal, pectoral, shoulders, paravertebral musculature). Also exercises for the most weakened and needy muscle groups during pregnancy, the aim is to avoid muscular decompensation.

IV. Coordination and balance exercises: simple tasks of eye-hand and eye-foot coordination with sports equipment, as well as body axis balance exercises.

V. Strengthening the pelvic floor muscles, Kegel exercises will be applied and is basically composed of contractions (slow and fast) of the different structures of the pelvic floor musculature.

VI. Relaxing section during 7-8 minutes, aiming to gradually lower the intensity of work with flexibility-stretching and relaxation exercises.

VII. Final Talk. This part is intended for pregnant women to express clearly and openly the sensations and perceptions experienced during the session. The reflection of each participant on the effect of physical practice is sought, not only in the physical or physiological aspect but also in the psychic and emotional section. The exchange of impressions between the pregnant women enhances the role of a correctly designed and conducted physical exercise program, as a social mobile of maintenance and improvement of the quality of life of the pregnant woman.

Study Type

Interventional

Enrollment (Anticipated)

500

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 Contact

Study Locations

      • Madrid, Spain, 28040
        • Recruiting
        • Facultad de Ciencias de la Actividad Física y el Deporte - INEF
        • Principal Investigator:
          • Rubén Barakat, Dr
        • Sub-Investigator:
          • Cristina Silva-Jose, Msc
        • Sub-Investigator:
          • Ángeles Blanco, Dr
        • Sub-Investigator:
          • Ignacio Refoyo, Dr
        • Sub-Investigator:
          • Miguel Sanchez-Polan, Msc
        • Contact:
        • Sub-Investigator:
          • Maia Brik, Dr
        • Sub-Investigator:
          • Tirso Perez, Dr
        • Sub-Investigator:
          • Javier Coterón, Dr
        • Sub-Investigator:
          • Vanessa Carrero Martinez, Dr
        • Sub-Investigator:
          • Laura de Mingo Romanillos, Dr
        • Sub-Investigator:
          • Irene Fernandez Buhigas, Dr
        • Sub-Investigator:
          • Fatima Garcia Benasach, Dr
        • Sub-Investigator:
          • Carmen Orizales Lago, Dr
        • Sub-Investigator:
          • Montse Palacio, Dr
        • Sub-Investigator:
          • Adriana Aquise Pino, Dr
        • Sub-Investigator:
          • Mar Gil Mira, Dr
        • Sub-Investigator:
          • Aranzazu Martin Arias, Dr

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 45 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

- Pregnant women fulfilling the following criteria: >18 years old, singleton pregnancies and planning management and delivery at the research hospitals, and also do not participate in any other program of supervised physical exercise.

Exclusion Criteria:

Women with absolute contraindications. Women with relative contraindications need permission from obstetric care providers prior to participation:

Absolute contraindications to exercise:

  • Ruptured membranes.
  • Premature labor.
  • Unexplained persistent vaginal bleeding.
  • Placenta praevia after 28 weeks gestation.
  • Pre-eclampsia.
  • Incompetent cervix.
  • Intrauterine growth restriction.
  • High-order multiple pregnancies (eg, triplets).
  • Uncontrolled type I diabetes.
  • Uncontrolled hypertension.
  • Uncontrolled thyroid disease.
  • Other serious cardiovascular, respiratory, or systemic disorders.

Relative contraindications to exercise:

  • Recurrent pregnancy loss.
  • Gestational hypertension.
  • A history of spontaneous preterm birth.
  • Mild/moderate cardiovascular or respiratory disease.
  • Symptomatic anemia.
  • Malnutrition.
  • Eating disorder.
  • Twin pregnancy after the 28th week.
  • Other significant medical conditions.

Women in the CG were asked about their exercise once each trimester using a "Decision Algorithm" and those who are excessively actives were excluded.

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: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control group
Women randomly assigned to the control group (CG) received general advice from their health care provider about the positive effects of physical activity. Participants in the CG had their usual visits with health care providers during pregnancy, which were equal to the exercise group. Women were not discouraged from exercising on their own. However, women in the CG were asked about their exercise once each trimester using a "Decision Algorithm" (by telephone).
Experimental: Exercise group

The design of the physical exercise program will be supported by the Canadian and Spanish Guidelines for exercise throughout pregnancy and published by Barakat model.

Frequency: The program will consist of three weekly sessions. The duration of every session will be 55-60 minutes. The intensity of the workload will be 55-60% of the maximum maternal Heart Rate, and controlled by Polar monitor (FT60). Likewise, once a week, the Borg Scale of Perceived Effort will be administered to participants, in order to have a more reliable assessment of the intensity of the activities, 12-14 (moderate; out of a 20 point scale) will be the level used.

The minimum adherence required for the participants will be 80% of the total sessions (approximately 80 sessions).

Exercise program All sessions will begin with a warm-up of 7-8 minutes composed of mild movements and joint mobility of upper and lower limbs exercises. Then a central part of 35-40 minutes, four types of activities will be included (aerobic work, muscle strengthening, coordination/balance tasks, pelvic floor exercises), finally a section of flexibility, relaxation, and final talk (comments and sharing) will be performed (12-15 minutes).

Healthy lifestyle advise This intervention consists of providing guidelines and videos with advice on healthy habits throughout the pregnancy process. This type of content will be related to daily physical activity, food recommendations, and fundamental exercises to perform during pregnancy.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Prenatal depression (CES-D)
Time Frame: 9 months
analyze with a questionnaire the variability during pregnancy (Likert scale 0-3)
9 months
Prenatal anxiety, State-Trait Anxiety Inventory (STAI)
Time Frame: 9 months
analyze with a questionnaire the value and its interrelationship with physical exercise patterns (Likert scale 0-3)
9 months
Prenatal stress, Perceived Stress Scale (PSS)
Time Frame: 9 months
analyze with a questionnaire the value and its interrelationship with physical exercise patterns(Likert scale 0-3)
9 months
Postnatal depression, Edinburgh Postnatal Depression Scale (EPDS).
Time Frame: 6 months
analyze with a questionnaire the value and its interrelationship with physical exercise during pregnancy(Likert scale 0-5)
6 months
Postnatal anxiety, State-Trait Anxiety Inventory (STAI)
Time Frame: 6 months
analyze with a questionnaire the value and its interrelationship with physical exercise patterns (Likert scale 0-3)
6 months
Postnatal stress, PSS (Perceived Stress Scale)
Time Frame: 6 months
analyze with a questionnaire the value and its interrelationship with physical exercise patterns(Likert scale 0-5; higher scores mean a worse outcome)
6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Maternal weight gain
Time Frame: 9 months
analyze the increase during pregnancy
9 months
Behavior of Fetal Heart Rate
Time Frame: 3 months
analyze variability during pregnancy
3 months
Maternal pains during pregnancy (headache, back pain, pelvic pain, paravertebral, scapular, etc.)
Time Frame: 9 months
analyze the value and its interrelationship with physical exercise patterns
9 months
Delivery tears
Time Frame: 1 month
analyze the value and its interrelationship with physical exercise patterns
1 month
Postpartum recovery of pre-pregnancy weight
Time Frame: 12 months
analyze how it varies during postpartum period
12 months
Placental angiogenic factors
Time Frame: measured at 24-25 weeks and at 34-35 weeks
placental growth factor (PIGF)
measured at 24-25 weeks and at 34-35 weeks
Blood pressure
Time Frame: 9 months
analyze how it varies during pregnancy
9 months
O'Sullivan test (OGTT)
Time Frame: 1 month
analyze the value and its interrelationship with physical exercise patterns
1 month
Urinary Incontinence Questionnaire (ICIQ-SF)
Time Frame: 9 months
analyze with a questionnaire the value and its interrelationship with physical exercise patterns (different measures in the questionnaire)(Likert scale 0-5; higher scores mean a worse outcome)
9 months
Gestational age
Time Frame: 9 months
analyze the value and its interrelationship with physical exercise patterns
9 months
Type of delivery (Vaginal, instrumental or cesarean)
Time Frame: 1 month
analyze whether women have had a vaginal, instrumental, or cesarean delivery and its interrelationship with physical exercise patterns
1 month
Duration of labor
Time Frame: 1 month
analyze the value and its interrelationship with physical exercise patterns
1 month
Birthweight
Time Frame: 1 month
analyze the value and its interrelationship with physical exercise patterns
1 month
Child's weight
Time Frame: 24 months
analyze the value and its interrelationship with physical exercise patterns during pregnancy
24 months
Child's height
Time Frame: 24 months
analyze the value and its interrelationship with physical exercise patterns during pregnancy
24 months
Mental assessment of the child (depression questionnaire adapted to childhood)
Time Frame: 24 months
analyze the value and its interrelationship with physical exercise patterns during pregnancy (Likert scale 0-3)
24 months
Psychomotor behavior of the child
Time Frame: 24 months
analyze some variables (sitting, crawling, standing, walking, holding objects...) and its relationship with maternal exercise
24 months
Fetal growth and development
Time Frame: 9 months
analyze the value and its interrelationship with physical exercise patterns
9 months
Performing episiotomy during childbirth
Time Frame: 1 month
analyze the appearance (descriptive: yes/no) and its interrelationship with physical exercise patterns
1 month
Apgar Score
Time Frame: 1 month
analyze the value and its interrelationship with physical exercise patterns (1 to 10)
1 month
Birth length
Time Frame: 1 month
analyze the value and its interrelationship with physical exercise patterns
1 month
Head circumference
Time Frame: 1 month
analyze the value and its interrelationship with physical exercise patterns
1 month
Landau reflexes test
Time Frame: 1 month
analyze the value and its interrelationship with physical exercise pattern
1 month
Neonatal intensive care unit (NICU)
Time Frame: 1 month
analyze the number of admissions and its interrelationship with physical exercise patterns
1 month
Umbilical cord Ph
Time Frame: 1 month
analyze the value and its interrelationship with physical exercise patterns
1 month
Fetal development
Time Frame: 9 months, once a trimester
analyze variables (estimated fetal weight, Fetal cardiac function, fetal measures, uterine arteries...) by ultrasound
9 months, once a trimester
Carotid intima-media thickness (CIMT)
Time Frame: 9 months
Measurement of carotid intima-media thickness (CIMT) with B-mode ultrasound is a noninvasive, sensitive, and reproducible technique for identifying and quantifying subclinical vascular disease and for evaluating cardiovascular disease (CVD) risk.
9 months
Maternal sleep habits
Time Frame: 9 months
analyze with Pittsburgh´s sleep quality index (Likert scale 0-5; higher scores mean a worse outcome)
9 months
Maternal body self-perception
Time Frame: 9 months
analyze using Ben-Toby Walker Body Attitude Questionnaire (Likert scale 0-5; higher scores mean a worse outcome)
9 months
Newborn sleep habits
Time Frame: 24 months
analyze using Brief Infant Sleep Questionnaire (Likert scale 0-5; higher scores mean a worse outcome)
24 months
Perception of health status - Short Form 36 health scale
Time Frame: 9 months
analyze the value and its interrelationship with physical exercise patterns (Likert scale 0-5; higher scores mean a better outcome)
9 months
Placental angiogenic factors
Time Frame: measured at 24-25 weeks and at 34-35 weeks
soluble fms-like tyrosinekinase-1 (sFlt1)
measured at 24-25 weeks and at 34-35 weeks
Lipidic profile
Time Frame: measured at 24-25 weeks and at 34-35 weeks
( Total Cholesterol, LDL-Cholesterol, HDL- Cholesterol, Tryglicerids)
measured at 24-25 weeks and at 34-35 weeks

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Maternal habits of physical activity - Pregnancy Physical Activity Questionnaire (PPAQ)
Time Frame: 12 months
analyze with a questionnaire how it varies during and after pregnancy
12 months
Recovery of pelvic floor muscles ultrasound
Time Frame: 6 months
analyze the diameter and thickness of muscles in the perineal area and their interrelationship with physical exercise patterns
6 months
Pregestational maternal patterns
Time Frame: 9 months
analyze sociodemographic and behavioral habits like (smoking, alcoholism, previous illness, COVID-19, parity, occupation, previous miscarriage...)
9 months
Coronavirus disease
Time Frame: 9 months
analyze the coronavirus condition during pregnancy and its interrelationship with other variables
9 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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)

March 17, 2022

Primary Completion (Anticipated)

January 1, 2024

Study Completion (Anticipated)

December 30, 2025

Study Registration Dates

First Submitted

March 24, 2022

First Submitted That Met QC Criteria

March 24, 2022

First Posted (Actual)

March 25, 2022

Study Record Updates

Last Update Posted (Actual)

July 1, 2022

Last Update Submitted That Met QC Criteria

June 28, 2022

Last Verified

June 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • Gestactive2022

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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