IMR Press / CEOG / Volume 50 / Issue 1 / DOI: 10.31083/j.ceog5001009
Open Access Systematic Review
The Effects of Different Exercise Programs on the Prevention of Perinatal Depression: A Systematic Review and Meta-Analysis
Show Less
1 School of Nursing, Guangdong Pharmaceutical University, 510310 Guangzhou, Guangdong, China
*Correspondence: xyyan@gdpu.edu.cn (Xiao-ying Yan)
Academic Editor: Johannes Ott
Clin. Exp. Obstet. Gynecol. 2023, 50(1), 9; https://doi.org/10.31083/j.ceog5001009
Submitted: 23 August 2022 | Revised: 1 November 2022 | Accepted: 2 November 2022 | Published: 6 January 2023
Copyright: © 2023 The Author(s). Published by IMR Press.
This is an open access article under the CC BY 4.0 license.
Abstract

Background: To evaluate the preventive effect of different exercise programs on perinatal depression and to provide practical suggestions to guide the maternal daily exercise plan. Methods: Nine electronic bibliographic databases were searched from inception until 18 January 2022. Meta-analysis of all data was performed using RevMan 5.4. Results: Sixteen RCTs consisting of 2233 maternal cases were included. Compared to women in the control group, women who received exercise effectively prevented maternal perinatal depression (Std. mean difference [SMD] = –1.31, 95% confidence interval [CI] –1.40 to –1.21). Prenatal exercise (SMD = –1.45), aerobic exercise (SMD = –1.78), personal exercise (SMD = –2.03), <30 minutes per single duration (SMD = –1.84), >3 times a week (SMD = –1.91) was the best preventive measure of maternal depression. Conclusions: Exercise can effectively improve the mental health status of perinatal pregnant women, and different exercise start time, exercise content, exercise frequency, exercise form, and single duration of exercise can improve depressive symptoms differently. It is recommended that pregnant women begin from the prenatal period of personal aerobic exercise 3 times a week, each exercise lasting less than 30 minutes, and adjust appropriately according to their own physical conditions.

Keywords
exercise
perinatal depression
preventive effect
meta-analysis
1. Introduction

Perinatal depression (PDN) is a psychiatric disorder that occurs during pregnancy (prenatal depression) or within one year after delivery (postpartum depression (PPD)) [1, 2]. The prevalence of PDN ranges from 11.4% to 17.4% worldwide [3, 4]. PDN can directly affect maternal health and pregnancy outcomes [5]. Therefore, preventing the occurrence of PDN becomes particularly important.

At present, the primary methods to treat PDN include drug treatment and psychotherapy; however, there are side effects of drug intervention, and the cost of psychotherapy is relatively high. Exercise intervention has the advantage of low cost and is easy to complete, attracting wide attention from scholars at home and abroad [6]. Studies have shown that exercise intervention can relieve PDN; however, existing research primarily focuses on the effect of exercise on improving the symptoms of perinatal women with a history of depression [7]. There are few reports of perinatal women with no history of depression before pregnancy being able to prevent depression by exercising during the perinatal period. This study conducts a meta-analysis of perinatal exercise research and reveals the prevention effect of exercise on PDN, analyzes the influence of different exercise programs on PDN, and explores an ideal exercise plan to prevent PDN.

2. Materials and Methods

The systematic review and meta-analysis were conducted following the PRISMA guidelines [8] and registered at the International Prospective Register of Systematic Reviews (CRD42022314645).

2.1 Search Strategy

We systematically searched five English databases (PubMed, Web of Science, The Cochrane Library, EBSCO, and APA/PsycNET) and four Chinese databases (CNKI, CBM, WanFang, and VIP) from their inception to 18 January 2022. Three groups of terms were combined according to the syntax rules for each database: (1) Perinatal period-related terms, including puerpera, pregnancy, expectant mother, antenatal, postpartum period, puerperium, postpartum care, postnatal care, and perinatal care; (2) exercise-related terms, including sports, exercise, physical activity, movement behavior, yoga, walking, running, jogging, swimming, aerobic, anaerobic, and pilates; (3) depression-related terms, including depressive symptoms, depression, depressive disorder, PDN, baby blues, mental health, psychological health, psychological function, mental function, and psychological. In addition to the digital bibliographic databases, we searched the Chinese clinical trial registry and World Health Organization (WHO) international clinical trial registry for unpublished trials relevant to this systematic review.

2.2 Inclusion and Exclusion Criteria
2.2.1 Types of Participants

(1) Pregnant women and women within one year after delivery were included. (2) Patients with psychiatric disorders were excluded. (3) Pregnant women with a history of depression, that is, if they met one of the following criteria, were excluded: ① score 13 on the Edinburgh Postpartum Depression Scale (EPDS); ② score 54 on the Self-rated Depression Scale (SDS); ③ score 11 on Hospital Anxiety and Depression Scale (HADS); ④ Health-related Quality of Life (HRQoL) Questionnaire: score 42 indicates the risk of depression; ⑤ score 15 on Center for Epidemiological Survey, Depression Scale (CES-D).

2.2.2 Intervention Group

The women in the intervention group underwent regular exercise for a fixed period. The various sub-elements analyzed included exercise start time, exercise content, exercise frequency, practice form, and duration of exercise.

2.2.3 Control Group

The women in the control group received routine care, including psychological care and health education, but did not practice any form of exercise intervention.

2.2.4 Outcome Measures

The primary outcome measure was depression symptoms, determined using the following scales: Edinburgh Postpartum Depression Scale (EPDS) 13 points, Self-rated Depression Scale (SDS) 54 points, Hospital Anxiety and Depression Scale (HADS) 11 points, Center for Epidemiological Survey, Depression Scale (CES-D) 15 points, and Health-related Quality of Life (HRQoL) Questionnaire 42 points.

2.2.5 Types of Study

Randomized control trials (RCTs) were included.

2.3 Study Selection

Endnote X9 software (Thomson Scientific, Philadelphia, PA, USA) was used to import all references and remove duplicates. Two independent authors evaluated the remaining studies according to inclusion and exclusion criteria first by screening the abstract and then the full text of potentially relevant papers. Any disagreements with respect to eligibility were resolved by a third independent author (H.C.H.).

2.4 Assessment of the Risk of Bias

Two authors (S.Y.M. and Y.L.) independently evaluated the risk of bias of eligible studies using the Cochrane Risk of Bias assessment tool [9], which evaluates for presence of selection bias, performance bias, detection bias, attrition bias, reporting bias, and other biases. According to the evaluation criteria, each item was classified as low, high, and unclear. Any disagreements were resolved by a third independent author (X.Y.Y.).

2.5 Data Extraction

Two authors (S.Y.M. and Y.L.) independently extracted relevant data from eligible articles, including the author, sample size, age, intervention, control, start time of exercise, exercise content, exercise frequency, practice form, single duration of exercise and results. Any differences between the two authors (S.Y.M. and Y.L.) were resolved by a third author (X.Y.Y.).

2.6 Synthesis and Analysis of Data

Statistical analysis was performed using RevMan 5.4 (Nordic Cochrane Centre, Hillerød, Denmark). Std. Mean differences (SMDs) and 95% confidence intervals (CIs) were calculated for continuous results. I2 was adopted to assess for heterogeneity among the included studies. If there was heterogeneity among studies (I2 > 50%), the random effect model was used for meta-analysis. If there was no significant heterogeneity among studies (I2 50%), the fixed effect model was applied. If there was significant heterogeneity, a subgroup analysis or sensitivity analysis was performed to explore the source of heterogeneity [10, 11].

3. Results
3.1 Search Results

This search strategy yielded 4596 potentially relevant citations from the nine electronic databases. Following the removal of 651 duplicate records, 3661 articles were excluded based on the selection of titles and abstracts, and the remaining 284 studies were evaluated in full text. Another 268 studies were excluded from the full text evaluation and a total of sixteen studies [12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27] were included in the final analysis (Fig. 1).

Fig. 1.

Database search flow diagram.

3.2 Description of Included Studies

A total of 16 randomized controlled trials (RCTs) were selected for analysis. The RCTs were conducted in four countries—China, Spain, the U.S. and Australia—and published between 2010–2021. The studies included 2233 participants [12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27]): 1124 (50.3%) in the intervention group and 1109 (49.7%) in the control group. The participants’ age ranged from 25 to 37. The baseline characteristics of the 16 RCTs were comparable between the two groups, and each RCT evaluated the preventive effect of exercise on PDN. A detailed summary is shown in Table 1 (Ref. [12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27]).

Table 1.Characteristics of 16 included RCTs.
First author Particular year Country/ region Age Sample capacity Exercise programs Outcomes
I C I C Start time Content Frequency Duration Form
Gao [14] 2021 China 27.92 ± 2.81 28.63 ± 2.80 19 12 postpartum yoga 3 times/week >60 min personal
Yan [12] 2021 China 36.65 ± 1.88 36.85 ± 2.63 100 106 prenatal dance gymnastics >3 times/week 30–60 min combination
Wu [19] 2019 China 32.24 ± 4.58 32.6 ± 5.05 34 35 prenatal aerobic exercise >3 times/week 30–60 min combination
Hu [15] 2020 China 25.16 ± 3.47 25.08 ± 3.35 49 49 prenatal aerobic exercise >3 times/week >60 min combination
Tang [25] 2014 China 2330 100 100 prenatal dance gymnastics >3 times/week <30 min personal
Ming [20] 2019 China 26.35 ± 4.72 27.85 ± 5.06 80 80 prenatal dance gymnastics >3 times/week N/A personal
Huang [16] 2020 China 35 280 280 prenatal aerobic exercise 3 times/week <30 min group
Fan [22] 2017 China 25.89 ± 4.17 26.02 ± 4.11 80 80 prenatal yoga 3 times/week N/A personal
Li [13] 2021 China 31.15 ± 1.21 30.21 ± 1.01 40 40 prenatal aerobic exercise >3 times/week N/A N/A
Wang [23] 2017 China 34.33 ± 2.01 31.82 ± 1.93 30 30 prenatal aerobic exercise >3 times/week <30 min N/A
Rodriguez [17] 2020 Spain 32.12 ± 4.43 30.58 ± 4.75 65 64 prenatal water sports 3 times/week >60 min group
Gallagher [18] 2019 USA 30.44 ± 6.17 27.65 ± 7.46 48 31 prenatal yoga 3 times/week <30 min personal
Yi [27] 2007 TaiWan 34.17 ± 3.20 34.33 ± 3.53 31 30 prenatal yoga 3 times/week >60 min group
Norman [26] 2010 Australia 29.3 ± 4.0 30.1 ± 5.3 62 73 postpartum strength exercise 3 times/week >60 min group
Aguilar [21] 2018 Spain 34.52 ± 4.50 33.67 ± 5.37 16 22 prenatal water sports >3 times/week >60 min group
Perales [24] 2014 Spain 31.08 ± 3.39 31.66 + 3.86 90 77 prenatal aerobic exercise >3 times/week 30–60 min N/A
Note: I: Intervention Group; C: Control Group; ① EPDS; ② CES-D; ③ HADS; ④ SDS; ⑤ HRQOL .
3.3 The Assessment of Risk of Bias

The risk of bias analysis for the included RCTs is summarized in Fig. 2. Nine RCTs described the use of the random number table method to generate random sequences, and five RCTs described the use of the sealed envelope method for allocation and concealment. Of all RCTs, 14 RCTs had their patients and staff blinded, and six RCTs had their calculation results blinded. The results of 16 RCTs were considered complete and confirmed as low risk. Eight selective reporting for those RCTs were determined as unclear risk. 16 RCTs had a low risk in other possible biases.

Fig. 2.

Risk of bias graph.

4. Meta-Analysis
4.1 Preventive Effect in the Intervention Group and the Control Group.

16 RCTs were compared between the intervention group and the control group to evaluate the preventive effect of different exercise programs on PDN. The total heterogeneity test result was >50% among the included RCTs, so a random-effects model was used for meta-analysis. The results suggest that the remission of the depressive symptoms of women in the perinatal period after regular exercise of the intervention group was better than that of the control group, and the results were statistically significant (SMD = –1.31, 95% CI –1.40 to –1.21, p < 0.001) (Fig. 3).

Fig. 3.

Effects of exercise intervention on perinatal depression.

In order to explore the reasons for the high heterogeneity, through the sensitivity analysis by excluding the included studies one by one, the overall effect value did not change significantly during the one-by-one exclusion process, suggesting less bias caused by individual studies. Therefore, the relevant subgroup analysis was carried out.

4.2 Exercise Mode

Five sub-elements of the exercise intervention were analyzed: exercise start time, exercise content, exercise frequency, practice form, and duration of exercise.

4.2.1 Exercise Start Time

The results showed that both prenatal and postpartum exercise effectively prevented depression symptoms (p < 0.01). The effect of the antenatal intervention (SMD = –1.45, 95% CI = –1.56 to –1.35) was more pronounced than the effect of the postpartum intervention (SMD = –0.37, 95% CI = –0.63 to –0.10) (Table 2).

Table 2.Analysis of the effect of the exercise program on intervention in perinatal depress.
Variable Subunit Article offer measure Sample size Total number of samples SMD [95% CI] Two-tailed test
Z p
Start time Antenatal 13 2006 2233 –1.45 [–1.56, –1.35] 27.16 <0.001
Postpartum 3 227 –0.37 [–0.63, –0.10] 2.72 0.007
Sports content Yoga 4 331 2233 –1.34 [–1.59, –1.09] 10.55 <0.001
Comprehensive aerobic exercise 6 1034 –1.78 [–1.94, –1.63] 23.03 <0.001
water sports 2 167 –0.03 [–0.34, 0.28] 0.20 0.840
Dance gymnastics 3 566 –1.34 [–1.54, –1.15] 13.65 <0.001
Power movement 1 135 –0.24 [–0.58, 0.10] 1.38 0.170
Practice form Personal practice 7 770 2233 –2.03 [–2.21, –1.84] 21.89 <0.001
group practice 6 1090 –1.06 [–1.19, –0.92] 15.44 <0.001
Combination practice 3 373 –0.89 [–1.11, –0.66] 7.66 <0.001
Frequency 3 times/week 7 1155 2233 –1.01 [–1.91, –0.12] 2.22 0.030
>3 times/week 9 1078 –1.91 [–2.73, –1.10] 4.59 <0.001
Duration of exercise <30 min 4 899 1833 –1.84 [–2.00, –1.68] 22.78 <0.001
30–60 min 3 442 –0.49 [–0.68, –0.30] 5.05 <0.001
>60 min 6 492 –0.54 [–0.73, –0.35] 5.46 <0.001
4.2.2 Exercise Content

The types of exercise in the 16 RCTs included yoga, aerobics, dance gymnastics, water sports, and strength exercise. The effect of all types of exercise on depression was evaluated: yoga (SMD = –1.34, 95% CI = –1.59 to –1.09), aerobics (SMD = –1.78, 95% CI = –1.94 to –1.63), and dance gymnastics (SMD = –1.34, 95% CI = –1.54 to –1.15) had statistically significant effect on depression (p < 0.001). Water sports (SMD = –0.03, 95% CI = –0.34 to 0.28) and strength exercise (SMD = –0.24, 95% CI = –0.58 to 0.10), p > 0.05. The results showed that aerobics was the best exercise (Table 2).

4.2.3 Exercise Frequency

The exercise frequency was classified as 3 times a week and >3 times a week. The effect of exercise frequency on depression was as follows: 3 times a week: SMD = –1.01, 95% CI = –1.91 to –0.12); >3 times a week: SMD = –1.91, 95% CI = –2.73 to –1.10 (Table 2).

4.2.4 Duration of Exercise

The duration of a single exercise was divided into <30 min/session, 30–60 min/session, and >60 min/session. Exercise duration had the following effect on depression: <30 min/session: SMD = –1.84, 95% CI = –2.00 to –1.68; 30–60 min/session: SMD = –0.49, 95% CI = –0.68 to –0.30; and >60 min/session: SMD = –0.54, 95% CI = –0.73 to –0.35 (Table 2).

4.2.5 Practice Form

The practice form mainly included personal practice at home, group practice, and combination practice. Practice form effected depression as follows: personal exercise: SMD = –2.03, 95% CI = –2.21 to –1.84; group exercise: SMD = –1.06, 95% CI = –1.19 to –0.92; combined exercise: SMD = –0.89, 95% CI = –1.11 to –0.66 (p < 0.001) (Table 2).

5. Discussion
5.1 Main Findings

Related research has focused on intervention experiments and review analysis, This study by systematically reviewing 16 RCTs, evaluated and compared the effect of different exercise programs on the prevention of PDN. Evidence-based results showed that all exercises were effective in preventing PDN symptoms. Dipietro et al. [28] found that physical exercise is as effective as psychoactive drugs on the prevention of PDN.

5.2 Interpretation

The findings showed that prenatal exercise had a better effect in preventing PDN than postpartum exercise. According to related studies, the incidence of PPD is highly correlated with the presence of depression during pregnancy [29], indicating that prenatal depression is the strongest predictor of PPD. Exercise during pregnancy reduces prenatal depression and, consequently, the occurrence of PPD [30]. Thus, prenatal exercise is of great value in preventing PDN and promoting fetal development and smooth delivery [31].

Yoga, aerobics, and dance gymnastics effectively prevented depression, with aerobics achieving the best results. Based on the change in maternal body function and risks associated with exercise, walking and Baduanjin are the most common exercises for pregnant women [32]. These exercises promote the blood circulation and metabolism of the maternal body, improve cardiopulmonary function, and are conducive to fetal delivery and maternal body recovery [33].

To avoid fatigue and stress [34], pregnant women should not exercise too frequently or for a longer duration. Evidence-based results found that exercising >3 times a week for <30 min/session was the most effective in preventing depression. This finding corresponds with the American College of Obstetricians and Gynecologists’ (ACOG) recommendations for exercise for pregnant and postpartum women [35]. Related studies have suggested that continuous exercise for >45 min can threaten maternal safety by raising fetal body temperature, and advise pregnant women to rest every 15 min while exercising [36].

Personal exercise programs are more effective in improving PDN than other forms of exercise. This may be related to the advantages of individual exercise, which is not limited by time, place, and economy. However, compared to group practice, personal practice lacks the necessary exercise monitoring and technical support, and pregnant women tend to abandon the exercise programs. Research shows that only 23.6% of pregnant women in China insist on exercising, and the main reasons for not exercising include insecurity, lack of a strong will, and no companionship [37]. It is suggested that the rapidly advancing internet technology should be used to establish digital maternal sports management platforms and WeChat groups to develop personal maternal exercise programs [38] to prevent PDN.

5.3 Strengths and Limitations

This study analyzes only RCTs and provides strong evidence for evaluating the preventive effect of different exercise programs on PDN. However, there may be clinical heterogeneity affecting the results; more high-quality studies are required to verify the reliability of the results.

5.4 Implications for Practice and Research

Exercise is a low-cost strategy. This study summarizes the current situation of the preventive effect of different exercise programs on PDN, providing a basis for inspection for future clinical trials. Before designing exercise programs for pregnant women, medical personnel should be aware of their exercise history, including exercise duration and frequency.

6. Conclusions

To sum up, exercise is effective in preventing PDN. It is recommended that pregnant women follow a personalized aerobics exercise regime of <30 min for three times a week to effectively prevent the occurrence of PDN.

Future research will be expanded in the following aspects: (1) to improve the pertinence and adaptability of exercise intervention programs, that is, to optimize exercise programs and conduct precise training according to their pregnancy cycle, postpartum recovery cycle, maternal age and related complications. (2) Strengthen the monitoring of exercise intervention, that is, in view of the special changes of maternal physical function, heart rate and psychological changes, strengthen the monitoring of the exercise process from the aspects of maternal subjective perception, maximum heart rate and maximum oxygen consumption, so as to avoid the risk of maternal exercise to the maximum extent.

Author Contributions

SM and YL drafted this manuscript; XY made substantial contributions to the conception and design of the review; HH, SM and YL participated in the acquisition of the data, the analysis, and interpretation of the data; XY revised the article critically for important intellectual content; XY approved the version of the article to be published. All authors read and approved the final manuscript.

Ethics Approval and Consent to Participate

Not applicable.

Acknowledgment

Not applicable.

Funding

This research received no external funding.

Conflict of Interest

The authors declare no conflict of interest.

References
[1]
ACOG Committee Opinion No. 757 Summary: Screening for Perinatal Depression. Obstetrics and Gynecology. 2018; 132: 1314–1316.
[2]
Expert consensus on depression screening, diagnosis and treatment of perinatal depression of Obstetrics and Gynecology Branch of Chinese Medical Association. Chinese Journal of Obstetrics and Gynecology. 2021; 56: 521–527.
[3]
Woody CA, Ferrari AJ, Siskind DJ, Whiteford HA, Harris MG. A systematic review and meta-regression of the prevalence and incidence of perinatal depression. Journal of Affective Disorders. 2017: 219: 86–92.
[4]
Nisar A, Yin J, Waqas A, Bai X, Wang D, Rahman A, et al. Prevalence of perinatal depression and its determinants in Mainland China: A systematic review and meta-analysis. Journal of Affective Disorders. 2020; 277: 1022–1037.
[5]
Slomian J, Honvo G, Emonts P, Reginster J, Bruyère O. Consequences of maternal postpartum depression: a systematic review of maternal and infant outcomes. Women’s Health. 2019; 15: 1745506519844044.
[6]
Carter T, Bastounis A, Guo B, Jane Morrell C. The effectiveness of exercise-based interventions for preventing or treating postpartum depression: a systematic review and meta-analysis. Archives of Women’s Mental Health. 2019; 22: 37–53.
[7]
Pritchett RV, Daley AJ, Jolly K. Does aerobic exercise reduce postpartum depressive symptoms? A systematic review and meta-analysis. The British Journal of General Practice. 2017; 67: 684–691.
[8]
McInnes MDF, Moher D, Thombs BD, McGrath TA, Bossuyt PM, Clifford T, et al. Preferred reporting items for a systematic review and meta-analysis of diagnostic test accuracy studies: the PRISMA-DTA statement. The Journal of the American Medical Association. 2018; 319: 388–396.
[9]
Cumpston M, Li T, Page MJ, Chandler J, Welch VA, Higgins JP, et al. Updated guidance for trusted systematic reviews: a new edition of the Cochrane handbook for systematic reviews of interventions. The Cochrane Database of Systematic Reviews. 2019; 10: ED000142.
[10]
Debray TPA, Moons KGM, Riley RD. Detecting small-study effects and funnel plot asymmetry in meta-analysis of survival data: a comparison of new and existing tests. Research Synthesis Methods. 2018; 9: 41–50.
[11]
Guyatt GH, Oxman AD, Vist GE, Kunz R, Falck-Ytter Y, Alonso-Coello P, et al. GRADE: an emerging consensus on rating quality of evidence and strength of recommendations. British Medical Journal. 2008; 336: 924–926.
[12]
Yan F, Zhang HZ, Chen YW, Zhang LL. Effects of “Dancing for Birth” on postpartum depression in multiparous women with advanced maternal age. Chinese Nursing Management. 2021; 21: 1504–1509. (In Chinese)
[13]
Smith R, Michalopoulou M, Reid H, Riches SP, Wango YN, Kenworthy Y, et al. Application of psychotherapy combined with exercise therapy in the treatment of gestational diabetes. Psychological Monthly Journal. 2021; 16: 107–108.
[14]
Gao XJ, Jiang YW, Xu K, Ma R, Li WY. The effect of yoga intervention on physical and mental health of postpartum women. Journal of Henan Normal University (Natural Science Edition). 2021; 49: 113–120.
[15]
Hu YF. Effect of aerobic exercise during pregnancy on delivery outcome. China Modern Medicine. 2020; 27: 114–116.
[16]
Huang YW, Lin YH, Xiong XY. The influence of low-grade low-intensity aerobic exercise on the prenatal quality of life and maternal and infant outcomes of elderly pregnant women. Guangzhou Medicine. 2020; 51: 66–70.
[17]
Rodríguez-Blanque R, Aguilar-Cordero MJ, Marín-Jiménez AE, Menor-Rodríguez MJ, Montiel-Troya M, Sánchez-García JC. Water exercise and quality of life in pregnancy: a randomised clinical trial. International Journal of Environmental Research and Public Health. 2020; 17: 1288.
[18]
Gallagher A, Kring D, Whitley T. Effects of yoga on anxiety and depression for high risk mothers on hospital bedrest. Complementary Therapies in Clinical Practice. 2020; 38: 101079.
[19]
Wu XC, Wu KL, Sun XF, Cen MJ, Zhang LL. Effect of Professor DENG’s Baduanjin Exercise Combined with Five-element Music Therapy on Glucose and Lipid Metabolism and Mental Adjustment in Pregnant Women with Gestational Diabetes Mellitus. Journal of Guangzhou University of Traditional Chinese Medicine. 2019; 36: 1149–1155.
[20]
Ming F, Lei L. The influence of pregnant women gymnastics on maternal mental health and birth outcomes. Health Care Guide. 2019; 1: 270.
[21]
Aguilar-Cordero MJ, Sánchez-García JC, Rodriguez-Blanque R, Sánchez-López AM, Mur-Villar N. Moderate Physical Activity in an Aquatic Environment during Pregnancy (SWEP Study) and its Influence in Preventing Postpartum Depression. Journal of the American Psychiatric Nurses Association. 2019; 25: 112–121.
[22]
Fan R. Effect of health education and yoga training on maternal physical and mental health and birth outcomes. Contemporary Medicine. 2017; 23: 82–84.
[23]
Wang F, Wang M. Observation on the effect of psychological nursing combined with exercise therapy in gestational diabetes nursing. Electronic Journal of Practical Clinical Nursing. 2017; 2: 41–50.
[24]
Perales M, Refoyo I, Coteron J, Bacchi M, Barakat R. Exercise during Pregnancy Attenuates Prenatal Depression. Evaluation and the Health Professions. 2015; 38: 59–72.
[25]
Tang FY, Qiu ZJ, Wang CG. Effect of Health Protection Exercise in Pregnant Period and Systematic Health Education on Delivery Process and Postpartum Depression. Chinese Journal of Coal Industry Medicine. 2014; 17: 1708–1711.
[26]
Norman E, Sherburn M, Osborne RH, Galea MP. An exercise and education program improves well-being of new mothers: a randomized controlled trial. Physical Therapy. 2010; 90: 348–355.
[27]
Ko Y, Yang C, Chiang L. Effects of Postpartum Exercise Program on Fatigue and Depression during “Doing-the-Month” Period. Journal of Nursing Research. 2008; 16: 177–186.
[28]
Dipietro L, Evenson KR, Bloodgood B, Sprow K, Troiano RP, Piercy KL, et al. Benefits of physical activity during pregnancy and postpartum: an umbrella review. Medicine and Science in Sports and Exercise. 2019; 51: 1292–1302.
[29]
Ana Y, Lewis MG, van Schayck OCP, Babu GR. Is physical activity in pregnancy associated with prenatal and postnatal depressive symptoms?: Results from MAASTHI cohort study in South India. Journal of Psychosomatic Research. 2021; 144: 110390.
[30]
Davenport MH, McCurdy AP, Mottola MF, Skow RJ, Meah VL, Poitras VJ, et al. Impact of prenatal exercise on both prenatal and postnatal anxiety and depressive symptoms: a systematic review and meta-analysis. British Journal of Sports Medicine. 2018; 52: 1376–1385.
[31]
Jiang X, Tan ZK, Nie YJ. Meta-analysis of the effect of the physical exercise on maternal depression intervention. Journal of Wuhan University of Sport. 2021; 55: 71–78.
[32]
Tung C, Lee C, Lin S, Lin H. The Exercise Patterns of Pregnant Women in Taiwan. Journal of Nursing Research. 2014; 22: 242–249.
[33]
Zheng SN. The effect of the individualized aerobic exercise guidance for pregnant women on their delivery outcomes. Contemporary Medicine Theory Cluster. 2020; 18: 237–238.
[34]
Han LY, Chen DQ. Exercise Research Progress during pregnancy. International Journal of Obstetrics and Gynecology. 2016; 43: 556–560.
[35]
ACOG Committee Opinion No.804: Physical Activity and Exercise During Pregnancy and the Postpartum Period: Correction. Obstetrics and Gynecology. 2021; 138: 683.
[36]
Padayachee C. Exercise guidelines for gestational diabetes mellitus. World Journal of Diabetes. 2015; 6: 1033.
[37]
Zhou R, Ma Q. Research progress in motor behavior cognition of pregnant women during pregnancy. General Practice Care. 2016; 14: 1095–1098.
[38]
Liu Y, Zhang Y. Online platform of pregnant schools on the quality of pregnancy care in patients with gestational diabetes. Clinical Medical Research and Practice. 2022; 7: 154–157.
Share
Back to top