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ObesityMIGHTNCT02574767

Diet and Physical Activity Counseling and n3-long Chain (PUFA) Supplementation in Obese Pregnant Women

A study testing Lifestyle counseling, PUFA Supplementation and Routine diet & PA in people with Obesity and Pregnancy, run by University of Chile at 1 site in Chile.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

In Chile, 1 out of 4 pregnant women is obese (BMI > 30 kg/m2). This impacts negatively the health of the mother and the offspring during pregnancy. Lifestyle interventions are the primary prevention strategy for gestational diabetes in obese women; however, these interventions have shown null or limited effectiveness. Read more about this study

Who is it for?
Ages 18 to 40 years, women only
Conditions the study is for
Obesity, Pregnancy
What is being tested?
Lifestyle counseling, PUFA Supplementation and Routine diet & PA
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
1,002 participants
Where
1 siteChile
Study dates
Aug 2015to Feb 2019
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 40 years
  • Women only
  • No healthy volunteers
  • Adult

Who may be able to join

  • ≤14 weeks gestational age at first prenatal visit
  • Body mass index (BMI) >30 Kg/m2 at first prenatal visit
  • Have a singleton pregnancy
  • Plan to deliver at the "Sotero del Rio Hospital".

Who cannot join

  • Preexisting diabetes (known or diagnosed at first control (Fasting Plasma Glucose > 126 mg/dl or 2h plasma glucose > 200 mg/dl during an oral glucose tolerance test (OTTG))
  • Insulin or metformin use
  • Known medical or obstetric complications which restrict physical activity
  • History of eating disorders
  • High risk for hemorrhagic bleeding
  • High risk pregnancy according to national guidelines

Trial locations and contacts

1 site in 1 country.

Chile1 site
  • Institute of Nutrition and Food Technology

    Santiago

Other trials in Chile

About this study

Official title: Effectiveness on Maternal and Offspring Metabolic Control of a Home-based Dietary and Physical Activity Counseling and n3-long Chain Polyunsaturated Fatty Acids (PUFA) Supplementation in Obese Pregnant Women.

In Chile, 1 out of 4 pregnant women is obese (BMI > 30 kg/m2). This impacts negatively the health of the mother and the offspring during pregnancy. Lifestyle interventions are the primary prevention strategy for gestational diabetes in obese women; however, these interventions have shown null or limited effectiveness. In animals, n-3 long-chain polyunsaturated fatty acid (n3LC-PUFAs) have shown to increase insulin sensitivity through higher production and secretion of adipokines, enhanced fatty acids oxidation, reduction of lipogenesis, and direct anti-inflammatory effects; however evidence in humans and during pregnancy is still very limited. Combining a lifestyle intervention with n3LC-PUFAs supplementation could enhance the metabolic control of obese pregnant women. Objective: to assess the effectiveness of two prenatal nutritional interventions (home-based diet and physical activity counseling and/or n3LC-PUFAs supplementation) delivered to obese pregnant women in achieving better metabolic control in both the mother (lower incidence of gestational diabetes mellitus) and the offspring (lower incidence of macrosomia and lower prevalence of insulin resistance at birth).

Methods: this study is a cluster-randomized trial in which obese pregnant women from 12 primary health care centers (PHCC) will be stratified by socio-economic status (SES) and randomized to one of four parallel study arms. We will recruit 1000 women allocated to: 1 Home-based Diet and physical activity (PA) plus n3LC-PUFAs supplementation (Intervention Group 1, n=250); 2. Routine diet \& PA counseling care plus n3LC-PUFAs supplementation (Intervention Group 2, n=250); 3. Home-based Diet and Physical activity plus placebo for n3LC-PUFA supplementation (Intervention Group 3, n=250); 4. Routine diet \& PA counseling plus placebo (Control Group, n=250). Expected results: we expect that the intervention will contribute to achieving a better metabolic control during pregnancy. Ultimately, we expect that this study will contribute to advance the understanding of how to develop and implement effective actions to promote healthier pregnancies and therefore, healthier lives for mothers and their offsprings.

Read the detailed description

Obesity and related non-communicable chronic diseases (NCDs: cardiovascular diseases, cancer and diabetes) represent the main causes of death and disability in Chile as well as worldwide. They account for an important proportion of health-care costs and loss of productivity, overloading a country's economy, particularly in developing countries. From a population perspective, it is now clear that preventing the emergence of these conditions is the most effective approach; however most of the current policies fail to incorporate scientific knowledge and thus, are not effective or sustainable. There is now compelling evidence that although obesity and NCDs are mainly observed in adulthood, the risk for most of these conditions originates in the first 1000-days of life (i.e. from pregnancy to two years old). Maternal lifestyle and conditions during pregnancy (e.g. maternal obesity) could affect not only future maternal health, but also risk for NCDs in the next generation. Therefore, pregnancy is a critical window in the implementation of NCDs prevention strategies. Most of the interventions on diet and physical activity (PA) during pregnancy have focused on decreasing gestational weight gain (GWG). Recent meta-analyses of interventions have demonstrated that lifestyle interventions during pregnancy can have a positive effect on GWG. Beyond lifestyle interventions, other dietary interventions have been proposed such as probiotics, vitamin D or n-3 long chain polyunsaturated fatty acids (n3LC-PUFAs) supplementation. Regarding n3LC-PUFAs, differences in plasma fatty acid profiles between women with gestational diabetes (GDM) and women without GDM suggest a possible alteration in fatty acid metabolism in GDM. Data from systematic reviews show a consistent association between marine or algae oil supplementation with higher length of gestation, improvement in maternal mood and neural development. Nonetheless, few interventions on diet and PA have focused on metabolic control in obese women and their impacts have not been consistent. Additionally, few intervention studies have explored the effect of n3LC-PUFAs supplementation on pregnant women in the incidence of GDM, with no studies conducted in obese pregnant women. Therefore, combining an n3LC-PUFAs supplementation with a lifestyle intervention could enhance the metabolic control of obese pregnant women. We propose to evaluate the effects of an n3LC-PUFAs supplementation intervention among obese pregnant women (independently and combined with a diet and physical activity intervention) on metabolic control in mothers and their offspring.

In 2013 we started in 12 primary health clinics (PHCC) of the South East area of Santiago Chile a cluster randomized trial -the Chilean Maternal \& Infant Nutrition Cohort Study (CHiMINCs)- that aims to improve weight control during pregnancy and offspring growth during infancy by enhancing PHCC's maternal and infant weight monitoring systems as well as promoting breastfeeding. In the current study we propose to expand that effort trying to optimize metabolic control of obese pregnant women and their offspring by combining home-based diet and physical activity counseling and n3LC-PUFAs supplementation. Women who seek prenatal care in any of the 12 selected PHCC with <14 weeks gestation at first prenatal visit; body mass index (BMI) >30 Kg/m2 at first prenatal visit; have a singleton pregnancy will be asked to participate. We will recruit 1000 women; 250 women per arm of the study. After randomization, obese pregnant women in the intervention group 1 will receive home-based Diet \& Physical activity (PA) counseling plus n3LC-PUFAs oral supplementation based on Schizochytrium oil (S-oil) containing 800 mg docosahexaenoic (DHA) acid/day, which will be administered as capsular preparations containing 200 mg DHA/capsule (4 capsules/day). Obese pregnant women in the intervention group 2 will receive the standard education sessions included in the prenatal controls at PHCC but no home-based counseling sessions, plus n3LC-PUFAs supplementation of 800 mg of DHA. Obese pregnant women in the intervention group 3 will receive the home-based diet \& PA counseling sessions plus n3LC-PUFAs placebo that will consist of S-oil containing 200 mg DHA/day. Placebo will be administered as capsular preparations containing 50 mg DHA/capsule (4 capsules/day), given that evidence suggests that it would be unethical not to provide DHA during pregnancy. Placebo will be delivered in the same way that the n3LC-PUFA supplementation. The control group will receive routine diet \& PA PHCC counseling sessions plus placebo (4 capsules of 50 mg DHA per day). Measurements will be collected at baseline (<14 weeks of pregnancy), mid-pregnancy (24-28 weeks), and at delivery. Baseline and 24-28 weeks measurements will be carried out at home.

Analyses will be done according both to the "intention-to-treat" (i.e. effectiveness approach) and "per protocol" (i.e. efficacy approach) principles. In accordance with the 2×2 factorial design, the diet \& PA intervention (Intervention Groups 1 and 3) will be compared to the routine care intervention (Intervention Groups 2 and Control Group) and the n3LC-PUFAs supplementation intervention (Intervention Groups 1 and 2) will be compared to placebo (Intervention Group 3 and Control Group). To evaluate the effects of the two combined interventions the outcomes in each of the 3 intervened groups will be compared between them and with the outcomes in the control group. We expect that the intervention will contribute to achieving a better metabolic control during pregnancy. Ultimately, we expect that this study will contribute to advance the understanding of how to develop and implement effective actions to promote healthier pregnancies and therefore, healthier lives for mothers and their offsprings.

Conditions
Obesity, Pregnancy
Being tested
Lifestyle counseling, PUFA Supplementation, Routine diet & PA, PUFA placebo
Keywords
Weight gain, Fatty Acids, Omega-3
Medical subject headings
Obesity, Weight Gain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Lifestyle counselingBehavioural

    Obese pregnant women from PHCC randomized to this group will receive Home-based Diet \& Physical activity (PA) counseling. Home-based intervention will consider 2 home visits of one hour of duration. During this session dietary educational and behavioral will be discussed with the participants and their families tailoring the contents based on the specific contexts.

  • PUFA SupplementationDietary supplement

    Obese pregnant women from PHCC randomized to this group will receive n3LC-PUFAs oral supplementation based on Schizochytrium oil (S-oil) containing 800 mg docosahexaenoic (DHA) acid/day, which will be administered as capsular preparations containing 200 mg DHA/capsule (4 capsules/day).

  • Routine diet & PABehavioural

    Obese pregnant women from PHCC randomized to this group will receive will receive routine diet \& PA counseling (i.e. they will receive the standard education sessions included in the prenatal controls at PHCC but no home-based counseling sessions).

  • PUFA placeboDietary supplement

    Obese pregnant women from PHCC randomized to this group will receive capsular preparations containing 50 mg DHA/capsule (4 capsules/day), given that evidence suggests that it would be unethical not to provide DHA during pregnancy. Placebo will be delivered in the same way that the n3LC-PUFA supplementation.

Study groups in NCT02574767
Study groupRoleWhat they receive
Lifestyle counseling + PUFA supplementExperimentalHome-based Diet and Physical activity plus n3LC-PUFAs supplementation
Receives: Behavioral: Lifestyle counseling; Dietary Supplement: PUFA Supplementation
Routine diet & PA + PUFA SupplementationExperimentalRoutine Diet \& Physical Activity counseling care plus n3LC-PUFAs supplementation.
Receives: Dietary Supplement: PUFA Supplementation; Behavioral: Routine diet & PA
Lifestyle counseling + PUFA placeboExperimentalHome-based Diet and Physical Activity plus placebo for n3LC-PUFAs supplementation.
Receives: Behavioral: Lifestyle counseling; Dietary Supplement: PUFA placebo
Routine diet & PA + PUFA placeboPlacebo comparatorRoutine Diet \& Physical Activity counseling plus placebo for n3LC-PUFAs supplementation.
Receives: Behavioral: Routine diet & PA; Dietary Supplement: PUFA placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Gestational Diabetes Mellitus (GDM)

    According to ADA 2011 guidelines (fasting glucose ≥92 mg/dL and/or 2 h after ≥153 mg/dL)

    Measured: 24-28 weeks of gestation

  2. Macrosomia

    Birth weight greater than 4000 g

    Measured: At birth

  3. Prevalence of insulin resistance

    Prevalence of insulin resistance (IR) defined as cord blood homeostasis model assessment-estimated insulin resistance (HOMA-IR) > 2.60 at birth.

    Measured: At birth

Secondary outcomes (5)
  1. Low Birth Weight

    Birth weight below 2500 g

    Measured: At birth

  2. Excess weight gain during pregnancy

    Weight at delivery minus the pregestational weight

    Measured: Self reported pre-gestational weight, weight gain will be measured at least three times at 10-14, 24-28, 35-37 weeks of gestation, and also at delivery

  3. Pre-eclampsia

    Blood pressure ≥ 140 mm Hg systolic or ≥ 90 mm Hg diastolic

    Measured: 24-28 weeks of gestation

  4. Preterm delivery

    Child´s birth < 37 weeks gestational age

    Measured: At birth

  5. Proportions of cesareans

    Proportion of children delivered via cesarean section divided total of deliveries

    Measured: At birth

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted14 Oct 2015 (estimated)
  2. Study startAug 2015
  3. Primary completionFeb 2019
  4. Study completionFeb 2019

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
1,002 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02574767
Sponsor's protocol ID
Fondecyt #1150878
Acronym
MIGHT
Status last verified
Oct 2015
First submitted
7 Oct 2015
Last updated
30 May 2019
Results posted
No
Data monitoring committee
No

Publications

  • De Toro V, Alberti G, Dominguez A, Carrasco-Negue K, Ferrer P, Valenzuela R, Garmendia ML, Casanello P. Growth patterns in infants born to women with pregestational overweight/obesity supplemented with docosahexaenoic acid during pregnancy. J Pediatr Gastroenterol Nutr. 2024 Aug;79(2):371-381. doi: 10.1002/jpn3.12294. Epub 2024 Jun 24.

    PubMed 38922906
  • Garmendia ML, Casanello P, Flores M, Kusanovic JP, Uauy R. The effects of a combined intervention (docosahexaenoic acid supplementation and home-based dietary counseling) on metabolic control in obese and overweight pregnant women: the MIGHT study. Am J Obstet Gynecol. 2021 May;224(5):526.e1-526.e25. doi: 10.1016/j.ajog.2020.10.048. Epub 2020 Nov 2.

    PubMed 33152314
  • Garmendia ML, Corvalan C, Casanello P, Araya M, Flores M, Bravo A, Kusanovic JP, Olmos P, Uauy R. Effectiveness on maternal and offspring metabolic control of a home-based dietary counseling intervention and DHA supplementation in obese/overweight pregnant women (MIGHT study): A randomized controlled trial-Study protocol. Contemp Clin Trials. 2018 Jul;70:35-40. doi: 10.1016/j.cct.2018.05.007. Epub 2018 May 17.

    PubMed 29777864

Questions about this trial

What is this clinical trial studying?

A study testing Lifestyle counseling, PUFA Supplementation and Routine diet & PA in people with Obesity and Pregnancy, run by University of Chile at 1 site in Chile.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 30 May 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Chile. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Gestational Diabetes Mellitus (GDM) (time frame: 24-28 weeks of gestation). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02574767, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 May 2019.

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