Submitted Successfully!
To reward your contribution, here is a gift for you: A free trial for our video production service.
Thank you for your contribution! You can also upload a video entry or images related to this topic.
Version Summary Created by Modification Content Size Created at Operation
1 -- 2050 2022-11-18 08:38:25 |
2 format Meta information modification 2050 2022-11-21 03:13:22 |

Video Upload Options

Do you have a full video?

Confirm

Are you sure to Delete?
Cite
If you have any further questions, please contact Encyclopedia Editorial Office.
Zhou, Y.;  Guo, X.;  Mu, J.;  Liu, J.;  Yang, H.;  Cai, C. Research Trends of Physical Activity during Pregnancy. Encyclopedia. Available online: https://encyclopedia.pub/entry/35280 (accessed on 15 October 2024).
Zhou Y,  Guo X,  Mu J,  Liu J,  Yang H,  Cai C. Research Trends of Physical Activity during Pregnancy. Encyclopedia. Available at: https://encyclopedia.pub/entry/35280. Accessed October 15, 2024.
Zhou, Yanbing, Xian Guo, Jinhao Mu, Jingying Liu, Hongying Yang, Chenxi Cai. "Research Trends of Physical Activity during Pregnancy" Encyclopedia, https://encyclopedia.pub/entry/35280 (accessed October 15, 2024).
Zhou, Y.,  Guo, X.,  Mu, J.,  Liu, J.,  Yang, H., & Cai, C. (2022, November 18). Research Trends of Physical Activity during Pregnancy. In Encyclopedia. https://encyclopedia.pub/entry/35280
Zhou, Yanbing, et al. "Research Trends of Physical Activity during Pregnancy." Encyclopedia. Web. 18 November, 2022.
Research Trends of Physical Activity during Pregnancy
Edit

Physical activity (PA) during pregnancy has been proven beneficial to pregnant women, with a significant effect on ameliorating many severe gestational complications. Improvement of sedentary behaviour, lifestyle intervention through leisure-time PA, and preterm care are major research frontiers and have received extensive attention. 

physical activity bibliometric analysis physical activity pregnancy

1. Introduction

Pregnancy is a special life experience for most women. Increased blood volume and heart rate, weight growth, and also a transition in the center of gravity are all typical hormonal and physiological changes that can possibly occur. Many severe complications may be induced such as gestational diabetes mellitus (GDM), pre-eclampsia, and hypertension [1][2][3].
Physical activity (PA) during pregnancy was already noticed and considered beneficial during the 17th and 18th centuries [4]. However, whether it should be promoted or not remained controversial. Pregnant women were encouraged to exercise and walk to increase the volume of PA, but many types of physical activities like dancing and horse-riding were prohibited at the same time because it was believed that it might lead to a fetus’ head striking a mother’s pelvis [4]. One of the earliest PA guidelines for pregnant women was issued in 1912, stating walking was the best kind of exercise [5]. Many of the first studies that focused on the relationships between birth weight and PA were published in the 1980s, ascribing higher levels of occupational and household PA to lower birth weights [6]. Many epidemiological studies have assessed the relationship between PA and pregnancy outcomes during the last few decades [6][7], but effective evidence for adverse pregnancy outcomes is still lacking [7]. In 1985, the American College of Obstetricians and Gynecologists (ACOG) published the first guidelines on prenatal PA, emphasizing the safety of aerobic exercise, but recommending against high-intensity PA, such as running [8]. The revision by ACOG in 1994 removed the upper limit of the heart rate and duration of exercise [9]. In 2002, ACOG recommended pregnant women with no complications to commit 30-min PA with moderate intensity daily [10]. Similarly, the U.S. Department of Health and Human Services (USDHHS) issued the US PA Guidelines in 2008, suggesting pregnant women without medical complications perform at least 150 min of moderate-intensity PA per week [11].
PA has been globally recommended for decades, yet few populations achieve the suggested volume because of complicated reasons including but not limited to intrapersonal barriers (including pregnancy symptoms, family and child-rearing responsibilities, lack of personal motivation, etc.), additional interpersonal barriers (including lack of social support, overprotective family members, etc.) and environmental, organizational, and political factors [12].
Bibliometric analysis is a widely used research method that investigates particular structures, characteristics, and principles of science and technology by examining the research history, turning points, and most noteworthy research trends [13]. CiteSpace is a flexible, powerful, and widely used software in bibliometric analysis that uses a mapping knowledge domain to provide a vast amount of information about important research power, hotspots, and global trends [14][15]. After going through a systematic literature search, no bibliometric analysis studies on PA during pregnancy have been found published.

2. Physical Activity during Pregnancy

The development and evolution of research hotspots can be obtained by sorting out the clusters of keywords and burst keywords from CiteSpace operation. The aforementioned clusters can be generally divided into three aspects including PA patterns (#0 physical activity, #8 muscle strengthening), lifestyle, risk factors (#3 sitting time, #4 preterm birth, #6 risk factors), and pregnancy complications (#1 gestational diabetes, #2 oxidative stress, #5 insulin sensitivity). The noticeable keywords with the strongest burst in 2010–2015 included activity pattern, exercise, maternal exercise, endurance exercise, and leisure-time PA, which indicated that activity pattern was the prior research focus. In 2016–2022, the burst keywords of GDM and maternal obesity demonstrated that the research focus during this period had gradually shifted to the improvement of pregnant complications. Moreover, keywords such as lifestyle intervention, sedentary behavior, lifestyle, and prenatal care, with the strongest burst, entailed that the effect of lifestyle on pregnancy was also a research hotspot.
The amelioration of pregnancy complications by PA has been another research hotspot in recent years. “Risk factor” is a high-frequency keyword, with 321 citations and one main cluster, which mainly addressed GDM, gestational weight gain, anxiety, and depression, lower back pain, pelvic girdle pain, fetal responses, and birth weight. GDM has emerged as a highly cited keyword, a strong burst keyword, and a main cluster, showing it as a primary research hotspot. While weight, maternal obesity, and weight loss are all strong burst keywords, as well indicating that gestational weight gain and weight control are both essential research spots. Globally, half of all the females who are at childbearing age are overweight or obese [16], which potentially will trigger excessive gestational weight gain and increases the risk of developing GDM [16][17][18]. GDM is related to a higher incidence of negative pregnancy outcomes and a long-term risk of childhood obesity and type-2 diabetes in both mother and the infant. Nevertheless, excessive gestational weight gain, GDM, as well as the possible complications of obesity during pregnancy could be minimized with PA [18]. The 2018 PA Guidelines Advisory Committee reported a significant inverse relationship between PA and weight gain, risk of gestational diabetes mellitus or preeclampsia, and symptoms of depression or anxiety [13]. A former study suggested that for pregnant women with GDM, any form of PA that is sufficiently intense and prolonged can be beneficial [19]. A meta-analysis demonstrated that participating in prenatal PA reduces the risk of having GDM by 40% [20]. Anxiety and depression can be commonly observed in pregnant women, which may have a negative impact on the health of both the mother and fetus [21][22]. An incidence of 16% of depressive symptoms, 5% of severe depressive symptoms, and 27% of lifted prenatal anxiety was demonstrated in previous studies [22]. PA has been proven able to play a role as a psychotherapeutic to attenuate depression and anxiety by changing neurotransmitter and hormone levels that are linked to depression and enhancing the encouragement of self-efficacy [23][24][25][26]. Lower back pain and pelvic pain happened frequently in two-thirds of pregnant women as pregnancy advances [27]. A meta-analysis illustrated that multiple types of exercise obtain functions ameliorating back pain and pelvic pain involving aerobic exercise, muscle strengthening exercise, flexibility exercise, and stretching exercise [28]. Fetal responses and birth weight have been addressed a lot with the citations of health and preterm birth. On one hand, researchers have illustrated that fetuses give response during or after exercise as light-to-moderate increases in fetal heart rate of 10–30 beats per minute over the baseline [29][30]. On the other hand, despite this, women who tend to exercise vigorously during the third trimester have a greater possibility to deliver infants with weights 200–400 g less than those who do not [31][32]. Yet neither has observed an increased risk of fetal growth or preterm birth; rigorous exercise has been proven safe for fetuses and mothers in the second trimester, whether they are physically active or not [29][30][31][32].
“PA,” “exercise,” and “aerobic” are all highly cited keywords with citations of 365, 151 and 126, whilst “activity pattern,” “exercise, maternal exercise,” and “endurance exercise” are all strong burst keywords. Moreover, #0 physical activity and #8 muscle strengthening are both prevalent main clusters. Aerobic exercise was used the most widely during pregnancy [33]. Regular aerobic exercise during pregnancy has been proven efficient to improve or maintain physical fitness. Specifically, simple activities such as walking, cycling, swimming, or other modified activities like yoga, are all encouraged for pregnant women to regularly perform in every trimester [34][35]. Current recommendations state that healthy pregnant women should engage in 150 min or more of moderate-intensity aerobic activity each week [36][37]. This exercise should be carried out over the duration of the week and modified as necessary for health. For instance, pregnant women who engaged in aerobic exercise for 30–60 min per day, 2–7 times per week, were observed having a significantly lower risk of prenatal hypertensive disorders, gestational hypertension, and cesarean delivery than the sedentary group [38].
Guidelines reported that healthy pregnant women who are very active, or frequently engage in vigorous-intensity aerobic activity can continue the intensive training [33][36], such as strength training, or high-intensity interval training (HIIT). Research indicated that resistance exercise can achieve perceived physical and mental vigor, attenuate feelings of fatigue and low energy [39]. The strengthening of abdominal and back muscles could minimize the risk of lower back pain [34]. Noticeably, a quick rise in blood pressure and intra-abdominal pressure is triggered by heavy strength training during pregnancy, which may momentarily reduce blood flow to the fetus. However, resistance exercise with a modest to moderate load had no negative consequences during pregnancy [40]. Resistance exercise with elastic belts for 2–3 repetitive sets of movements, or through self-muscle exercises that involve upper and lower limbs for 2–3 sets of 12–24 repetitions, would fit well in pregnancy [41]. HIIT is the second most popular kind of exercise in the European fitness trends [42]. The intensity of training and interval section was monitored and measured by maximal heart rate or Borg’s rate of perceived exertion scale [43], meanwhile the ratio of exercise and rest time depends on individual capabilities, training progression, and pregnancy stage [44]. With regards to obstetric outcomes, HIIT programs were proven to be safe and well-accepted by pregnant women regardless of the training components and interval structure [45], even during the third trimester [46]. Nonetheless, the association between health outcomes and different type, timing, or domain of activity patterns cannot be assured due to insufficient research evidence [33].
Generally, PA during pregnancy with moderate intensity is agreed to be basically safe and beneficial for both mother and fetus [47][48][49]. However, exercise with contraindications is outside the purview of what an exercise expert is allowed to do. As official guidelines stated, women with absolute contraindications should be restricted from strenuous exercise. Women with relative contraindications should only participate in moderate-to-vigorous intensity PA with professional advice and obstetric care [37][50][51]. Gynecologists or other obstetric care professionals should thoroughly assess women with medical or obstetric complications before they begin the activities. Both active and inactive healthy women should start prenatal activities [34]. Women who suffered from complicated pregnancies (Gestational diabetes mellitus, high blood pressure, or other complications) also should continue their normal everyday activities and modify their exercise programs with qualified prenatal exercise specialists.
Given that “lifestyle intervention,” “leisure-time PA,” “sedentary behavior,” and “lifestyle” are all strong burst keywords, “sitting time” is one main cluster, and the effect of lifestyle intervention on pregnancy is one of the important research hotspots. Furthermore, “sedentary behavior” and “lifestyle” are also the newest strong burst keywords, which leads the effect of lifestyle intervention on pregnancy to be the research frontier on PA during pregnancy. Previous studies suggested that sedentary behaviour in pregnancy would probably lead to macrosomic infants, gestational weight gain, and hypertensive disorders [52], shorter gestation, and inhibited fetal growth [53]. That changing lifestyle during pregnancy by implementing leisure-time PA has been analyzed and discussed frequently in recent years [54][55][56]. A systematic review clearly showed that healthy expectant mothers can perform mild, moderate, and even vigorous levels of leisure-time PA without running the danger of giving birth prematurely [57]. A great number of previous cohort studies focused on diverse aspects can be found published, which is one of the foremost reasons why the #8 cohort study is presented as one main cluster. In maternal health, a systematic review that included seven cohort studies achieved controversial results, but generally, high-intensity leisure-time PA before and/or during pregnancy, or performing more than 4 h leisure-time PA each week may reduce the risk of pre-eclampsia [56]. A cohort study with 3209 participants suggested that leisure-time PA during both pre-pregnancy and early pregnancy reduced 46% of the risk of GDM compared with inactivity groups during both periods [58]. Meanwhile, another cohort study with 10,038 pregnant women illustrated that sustained low leisure-time PA during pregnancy is associated with excess risk of GDM and overall preterm birth. Moreover, women who increased leisure time PA lowered the rate of GDM. This could indicate that the increase in leisure-time PA in early pregnancy phases may be related to improved pregnancy health [59]. In offspring health, a cohort study proved that sons of women with light and moderate to heavy leisure-time PA had a lower risk of having a low intelligence score compared with sons of sedentary women [60]. Similarly, a systematic review and meta-analysis of 30 randomized controlled trials and 51 cohort studies supported the promotion of LTPA in pregnancy as a strategy to improve maternal and child health [61]. Furthermore, current cohort study results have also shown positive relationships between leisure-time PA and hyperemesis gravidarum [62], head circumference among male infants [63], birthweight among female infants, and women with normal prepregnancy BMI [63]. Conversely, no association was found between leisure-time PA and adiposity in mid-childhood [64] and intelligence quotient [65].

References

  1. Torosyan, N.; Aziz, D.; Quesada, O. Long-term sequelae of adverse pregnancy outcomes. Maturitas 2022, 165, 1–7.
  2. Persson, L.K.G.; Lihme, F.F.; Basit, S.; Larsen, M.O.; Scheller, N.M.; Andersen, A.S.; Halse, K.G.; Thorsen Meyer, A.; Sørensen, K.M.; Wohlfahrt, J. Cohort profile: The PreEclampsia, Angiogenesis, Cardiac dysfunction and Hypertension (PEACH) Study. Paediatr. Perinat. Epidemiol. 2022, 36, 863–878.
  3. Arechvo, A.; Voicu, D.; Gil, M.M.; Syngelaki, A.; Akolekar, R.; Nicolaides, K.H. Maternal race and preeclamp-sia: Cohort study and systematic review with meta-analysis. BJOG Int. J. Obstet. Gynaecol. 2022, 129, 2082–2093.
  4. Ribeiro, M.M.; Andrade, A.; Nunes, I. Physical exercise in pregnancy: Benefits, risks and prescription. J. Périnat. Med. 2022, 50, 4–17.
  5. Slemons, J.M. The Prospective Mother: A Handbook for Women During Pregnancy; Appleton: New York, NY, USA, 1912.
  6. Briend, A. Maternal physical activity, birth weight and perinatal mortality. Med. Hypotheses 1980, 6, 1157–1170.
  7. Morales-Suárez-Varela, M.; Clemente-Bosch, E.; Peraita-Costa, I.; Llopis-Morales, A.; Martínez, I.; Llopis-González, A. Maternal Physical Activity During Pregnancy and the Effect on the Mother and Newborn: A Systematic Review. J. Phys. Act. Health 2020, 18, 130–147.
  8. Temme, K.E. Exercise in Pregnancy and Postpartum; Springer: Berlin/Heidelberg, Germany, 2015; pp. 243–273.
  9. American College of Obstetricians and Gynecologists. Exercise during pregnancy and the postpartum period: ACOG technical bulletin number 189—February 1994. Int. J. Gynecol. Obstet. 1994, 45, 65–70.
  10. American College of Obstetricians and Gynecologists. Committee opinion: Exercise during pregnancy and the postpartum period. Obstet. Gynecol. 2002, 99, 171–173.
  11. Physical Activity Guidelines Advisory Committee. Physical Activity Guidelines Advisory Committee Report; Department of Health and Human Services: Washington, DC, USA, 2008.
  12. Koleilat, M.; Vargas, N.; Vantwist, V.; Kodjebacheva, G.D. Perceived barriers to and suggested interventions for physical activity during pregnancy among participants of the Special Supplemental Nutrition Program for Women, Infants, and Children (WIC) in Southern California. BMC Pregnancy Childbirth 2021, 21, 1–9.
  13. Chen, C. Science Mapping: A Systematic Review of the Literature. J. Data Inf. Sci. 2017, 2, 1–40.
  14. Synnestvedt, M.B.; Chen, C.; Holmes, J.H. CiteSpace II: Visualization and Knowledge Discovery in Bibliographic Databases; American Medical Informatics Association: Bethesda, MD, USA, 2005; Volume 2005, pp. 724–728.
  15. Chen, C. Searching for intellectual turning points: Progressive knowledge domain visualization. Proc. Natl. Acad. Sci. USA 2004, 101 (Suppl. S1), 5303–5310.
  16. Dodd, J.M.; Deussen, A.R.; Mitchell, M.; Poprzeczny, A.J.; Louise, J. Maternal overweight and obesity during pregnancy: Strategies to improve outcomes for women, babies, and children. Expert Rev. Endocrinol. Metab. 2022, 17, 343–349.
  17. Vargas-Terrones, M.; Nagpal, T.S.; Barakat, R. Impact of exercise during pregnancy on gestational weight gain and birth weight: An overview. Braz. J. Phys. Ther. 2018, 23, 164–169.
  18. Rasmussen, L.; Poulsen, C.W.; Kampmann, U.; Smedegaard, S.B.; Ovesen, P.G.; Fuglsang, J. Diet and Healthy Lifestyle in the Management of Gestational Diabetes Mellitus. Nutrients 2020, 12, 3050.
  19. Laredo-Aguilera, J.A.; Gallardo-Bravo, M.; Rabanales-Sotos, J.A.; Cobo-Cuenca, A.I.; Carmona-Torres, J.M. Physical Activity Programs during Pregnancy Are Effective for the Control of Gestational Diabetes Mellitus. Int. J. Environ. Res. Public Health 2020, 17, 6151.
  20. Davenport, M.H.; Ruchat, S.M.; Poitras, V.J.; Jaramillo, G.A.; Gray, C.E.; Barrowman, N.; Skow, R.J.; Meah, V.L.; Riske, L.; Sobierajski, F.; et al. Prenatal exercise for the prevention of gestational diabetes mellitus and hypertensive disorders of pregnancy: A systematic review and meta-analysis. Br. J. Sports Med. 2018, 52, 1367–1375.
  21. Xu, H.; Hutcheon, J.A.; Liu, X.; Stephansson, O.; Cnattingius, S.; Arkema, E.V.; Johansson, K. Risk of gestational diabetes mellitus in relation to early pregnancy and gestational weight gain before diagnosis: A population-based cohort study. Acta Obstet. Gynecol. Scand. 2022, 101, 1253–1261.
  22. Dragomir, C.; Popescu, R.; Jurca, M.A.; Laza, R.; Florian, R.I.; Dragomir, I.; Negrea, R.; Craina, M.; Dehelean, C.A. Postpartum Maternal Emotional Disorders and the Physical Health of Mother and Child. Psychol. Res. Behav. Manag. 2022, 15, 2927–2940.
  23. Campolong, K.; Jenkins, S.; Clark, M.M.; Borowski, K.; Nelson, N.; Moore, K.M.; Bobo, W.V. The association of exercise during pregnancy with trimester-specific and postpartum quality of life and depressive symptoms in a cohort of healthy pregnant women. Arch. Women’s Ment. Health 2017, 21, 215–224.
  24. Watson, S.J.; Lewis, A.J.; Boyce, P.; Galbally, M. Exercise frequency and maternal mental health: Parallel process modelling across the perinatal period in an Australian pregnancy cohort. J. Psychosom. Res. 2018, 111, 91–99.
  25. Rajaie, S.H.; Soltani, S.; Yazdanpanah, Z.; Zohrabi, T.; Beigrezaei, S.; Mohseni-Takalloo, S.; Kaviani, M.; Forbes, S.C.; Baker, J.S.; Salehi-Abargouei, A. Effect of exercise as adjuvant to energy-restricted diets on quality of life and depression outcomes: A meta-analysis of randomized controlled trials. Qual. Life Res. 2022, 31, 3123–3137.
  26. Howard, K.; Maples, J.M.; Tinius, R.A. Modifiable Maternal Factors and Their Relationship to Postpartum De-pression. Int. J. Environ. Res. Public Health 2022, 19, 12393.
  27. Ceprnja, D.; Chipchase, L.; Fahey, P.; Liamputtong, P.; Gupta, A. Prevalence and factors associated with pelvic girdle pain during pregnancy in Australian women: A cross-sectional study. Spine 2021, 46, 944.
  28. Davenport, M.H.; Marchand, A.; Mottola, M.F.; Poitras, V.J.; Gray, C.E.; Garcia, A.J.; Barrowman, N.; Sobierajski, F.; James, M.; Meah, V.L. Exercise for the prevention and treatment of low back, pelvic girdle and lumbopelvic pain during pregnancy: A systematic review and meta-analysis. Br. J. Sport. Med. 2019, 53, 90–98.
  29. Szymanski, L.M.; Satin, A.J. Exercise During Pregnancy: Fetal responses to current public health guidelines. Obstet. Gynecol. 2012, 119, 603–610.
  30. Artal, R.; Rutherford, S.; Romem, Y.; Kammula, R.K.; Dorey, F.J.; Wiswell, R.A. Fetal heart rate responses to maternal exercise. Am. J. Obstet. Gynecol. 1986, 155, 729–733.
  31. Kramer, M.S.; McDonald, S.W. Aerobic exercise for women during pregnancy. Cochrane Database Syst. Rev. 2006, 2006, D180.
  32. Lokey, E.A.; Tran, Z.V.; Wells, C.L.; Myers, B.C.; Tran, A.C. Effects of physical exercise on pregnancy outcomes: A meta-analytic review. Med. Sci. Sports Exerc. 1991, 23, 1234–1239.
  33. WHO. WHO Guidelines on Physical Activity and Sedentary Behaviour; World Health Organization: Geneva, Switzerland, 2020.
  34. Bisner, M.L.; Gyanfi-Bannerman, C. Physical activity and exercise during pregnancy and the postpartum period. ACOG 2020, 135, 178–188.
  35. RPDYKP, H.A.; Kocak, D.Y.; Akarsu, G.D. Experiences of Pregnant Women Participating in Antenatal Yoga: A Qualitative Study. Altern. Ther. Health Med. 2021, 28, 18–23.
  36. Piercy, K.L.; Troiano, R.P.; Ballard, R.M.; Carlson, S.A.; Fulton, J.E.; Galuska, D.A.; George, S.M.; Olson, R.D. The Physical Activity Guidelines for Americans. JAMA 2018, 320, 2020–2028.
  37. Mottola, M.F.; Davenport, M.H.; Ruchat, S.-M.; Davies, G.A.; Poitras, V.J.; Gray, C.E.; Garcia, A.J.; Barrowman, N.; Adamo, K.B.; Duggan, M.; et al. 2019 Canadian guideline for physical activity throughout pregnancy. Br. J. Sports Med. 2018, 52, 1339–1346.
  38. Magro-Malosso, E.R.; Saccone, G.; Di Tommaso, M.; Roman, A.; Berghella, V. Exercise during pregnancy and risk of gestational hypertensive disorders: A systematic review and meta-analysis. Acta Obstet. Gynecol. Scand. 2017, 96, 921–931.
  39. Nelson, R.K.; Hafner, S.M.; Cook, A.C.; Sterner, N.J.; Butler, E.L.; Jakiemiec, B.E.; Saltarelli, W.A. Exercise Dur-ing Pregnancy: What Do OB/GYNs Believe and Practice? A Descriptive Analysis. Women’s Health Rep. 2022, 3, 274–280.
  40. Garnæs, K.K.; Helvik, A.; Stafne, S.N.; Mørkved, S.; Salvesen, K.; Salvesen, Ø.; Moholdt, T. Effects of supervised exercise training during pregnancy on psychological well-being among overweight and obese women: Secondary analyses of the ETIP-trial, a randomised controlled trial. BMJ Open 2019, 9, e28252.
  41. Yaping, X.; Huifen, Z.; Chunhong, L.; Fengfeng, H.; Huibin, H.; Meijing, Z. A meta-analysis of the effects of re-sistance training on blood sugar and pregnancy outcomes. Midwifery 2020, 91, 102839.
  42. Batrakoulis, A. European Survey of Fitness Trends For 2020. ACSM’S Health Fit. J. 2019, 23, 28–35.
  43. Wood, G.; Murrell, A.; Van Der Touw, T.; Smart, N. HIIT is not superior to MICT in altering blood lipids: A sys-tematic review and meta-analysis. BMJ Open Sport Exerc. Med. 2019, 5, e647.
  44. Szumilewicz, A. HIIT vs. MICT during Pregnancy and Health and Birth Outcomes in Mothers and Children (HIIT MAMA). 2021. Available online: https://www.clinicaltrials.gov/ct2/show/NCT05009433 (accessed on 15 September 2022).
  45. Szumilewicz, A.; Santos-Rocha, R.; Worska, A.; Piernicka, M.; Yu, H.; Pajaujiene, S.; Shojaeian, N.; Caro, M.A.O. How to HIIT while pregnant? The protocol characteristics and effects of high intensity interval training implemented during pregnancy: A systematic review. Balt. J. Health Phys. Act. 2022, 14, 1–16.
  46. Beetham, K.S.; Giles, C.; Noetel, M.; Clifton, V.; Jones, J.C.; Naughton, G. The effects of vigorous intensity exercise in the third trimester of pregnancy: A systematic review and meta-analysis. BMC Pregnancy Childbirth 2019, 19, 1–18.
  47. Danielli, M.; Gillies, C.; Thomas, R.C.; Melford, S.E.; Baker, P.N.; Yates, T.; Khunti, K.; Tan, B.K. Effects of Su-pervised Exercise on the Development of Hypertensive Disorders of Pregnancy: A Systematic Review and Meta-Analysis. J. Clin. Med. 2022, 11, 793.
  48. Selman, R.; Early, K.; Battles, B.; Seidenburg, M.; Wendel, E.; Westerlund, S. Maximizing Recovery in the Post-partum Period: A Timeline for Rehabilitation from Pregnancy through Return to Sport. Int. J. Sport. Phys. Ther. 2022, 17, 1170–1183.
  49. Andersson-Hall, U.; de Maré, H.; Askeli, F.; Börjesson, M.; Holmäng, A. Physical activity during pregnancy and association with changes in fat mass and adipokines in women of normal-weight or with obesity. Sci. Rep. 2021, 11, 1–10.
  50. Tsakiridis, I.; Bakaloudi, D.R.; Oikonomidou, A.C.; Dagklis, T.; Chourdakis, M. Exercise during pregnancy: A comparative review of guidelines. J. Périnat. Med. 2020, 48, 519–525.
  51. Evenson, K.R.; Mottola, M.F.; Artal, R. Review of recent physical activity guidelines during pregnancy to facilitate advice by health care providers. Obstet. Gynecol. Surv. 2019, 74, 481–489.
  52. Wallace, M.K.; Jones, M.A.; Whitaker, K.; Gibbs, B.B. Patterns of physical activity and sedentary behavior before and during pregnancy and cardiometabolic outcomes. Midwifery 2022, 114, 103452.
  53. Jones, M.A.; Catov, J.M.; Jeyabalan, A.; Whitaker, K.M.; Barone Gibbs, B. Sedentary behaviour and physical activity across pregnancy and birth outcomes. Paediatr. Périnat. Epidemiol. 2021, 35, 341–349.
  54. Cai, C.; Zhang, Z.; Mcdonald, S.; Strom, C.; Skow, R.J.; May, L.E.; Steinback, C.D.; Davenport, M.H. Leisure-time physical activity before and during pregnancy is associated with improved insulin resistance in late pregnancy. Int. J. Environ. Res. Public Health 2021, 18, 4413.
  55. Caputo, E.L.; Domingues, M.R.; Bertoldi, A.D.; Ferreira, P.H.; Ferreira, M.L.; Shirley, D.; Da Silva, M.C. Are lei-sure-time and work-related activities associated with low back pain during pregnancy? BMC Musculoskelet. Disord. 2021, 22, 1–8.
  56. Wolf, H.T.; Owe, K.M.; Juhl, M.; Hegaard, H.K. Leisure Time Physical Activity and the Risk of Pre-eclampsia: A Systematic Review. Matern. Child Health J. 2013, 18, 899–910.
  57. Kahn, M.; Robien, K.; DiPietro, L. Maternal leisure-time physical activity and risk of preterm birth: A system-atic review of the literature. J. Phys. Act. Health 2016, 13, 796–807.
  58. Badon, S.E.; Wartko, P.D.; Qiu, C.; Sorensen, T.K.; Williams, M.A.; Enquobahrie, D.A. Leisure time physical ac-tivity and gestational diabetes mellitus in the omega study. Med. Sci. Sport. Exerc. 2016, 48, 1044.
  59. Catov, J.M.; Parker, C.B.; Gibbs, B.B.; Bann, C.M.; Carper, B.; Silver, R.M.; Simhan, H.N.; Parry, S.; Chung, J.H.; Haas, D.M.; et al. Patterns of leisure-time physical activity across pregnancy and adverse pregnancy outcomes. Int. J. Behav. Nutr. Phys. Act. 2018, 15, 1–10.
  60. Jochumsen, S.; Henriksen, T.B.; Lindhard, M.S.; Hegaard, H.K.; Rode, L. Physical activity during pregnancy and intelligence in sons; A cohort study. Scand. J. Med. Sci. Sports 2019, 29, 1988–1995.
  61. Da Silva, S.G.; Hallal, P.C.; Domingues, M.R.; Bertoldi, A.D.; Silveira, M.F.D.; Bassani, D.; Da Silva, I.C.M.; Da Silva, B.G.C.; Coll, C.D.V.N.; Evenson, K. A randomized controlled trial of exercise during pregnancy on maternal and neonatal outcomes: Results from the PAMELA study. Int. J. Behav. Nutr. Phys. Act. 2017, 14, 1–11.
  62. Owe, K.M.; Støer, N.; Wold, B.H.; Magnus, M.C.; Nystad, W.; Vikanes, Å.V. Leisure-time physical activity before pregnancy and risk of hyperemesis gravidarum: A population-based cohort study. Prev. Med. 2019, 125, 49–54.
  63. Pastorino, S.; Bishop, T.; Crozier, S.R.; Granström, C.; Kordas, K.; Küpers, L.K.; O'Brien, E.C.; Polanska, K.; Sauder, K.A.; Zafarmand, M.H. Associations between maternal physical activity in early and late pregnancy and offspring birth size: Remote federated individual level meta-analysis from eight cohort studies. BJOG Int. J. Obstet. Gynaecol. 2019, 126, 459–470.
  64. Navarro, P.; Mehegan, J.; Murrin, C.M.; Kelleher, C.C.; Phillips, C.M. for the Lifeways Cross Generation Cohort Study. Associations between a maternal healthy lifestyle score and adverse offspring birth outcomes and childhood obesity in the Lifeways Cross-Generation Cohort Study. Int. J. Obes. 2020, 44, 2213–2224.
  65. Na, X.; Raja, R.; Phelan, N.E.; Tadros, M.R.; Moore, A.; Wu, Z.; Wang, L.; Li, G.; Glasier, C.M.; Ramakrishnaiah, R.R. Mother’s physical activity during pregnancy and newborn’s brain cortical development. Front. Hum. Neurosci. 2022, 638, 943341.
More
Information
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : , , , , ,
View Times: 317
Revisions: 2 times (View History)
Update Date: 21 Nov 2022
1000/1000
ScholarVision Creations