Table 1.
Study details | Systematic review | Participants | Aims | Description of interventions |
---|---|---|---|---|
Author year, context/setting country |
Type of studies, number of studies included = n Meta‐analysis (MA), number of studies included in MA = mn Countries of origin of included studies Appraisal of studies, instrument used Reporting of review, checklist used Quality assessment, rating by Joanna Briggs Institute (JBI) checklist (0–11) |
Total number = N |
Details, characteristics of initiative Mode (of birth) Duration Follow‐up time (FU) Comparator(s) in randomized controlled trials (RCT), for example usual/standard care (UC) |
|
Buelo et al., 2019 (34) Scottish Collaboration for Public Health Research and Policy, School of Health in Social Science, University of Edinburgh, United Kingdom (UK) |
Quantitative (aim 1) Qualitative (aim 2) Mixed‐methods synthesis (aim 3) n = 28 RCT 12 Pre‐post studies 6 Interview 10 Australia 7 USA 5 Canada 4 China 1 Spain 1 Cochrane collaborations Risk of Bias Tool (RoB) Critical Appraisal Skills Programme (CASP) Preferred Reporting Items for Systematic Reviews and Meta‐Analyses (PRISMA) checklist JBI 10 1,2,3,4,5,6,7,8,10, 11 |
Women with previous gestational diabetes (GDM) N = 5,211 |
Explore
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Lifestyle interventions or PA only (diet, PA, breastfeeding/child nutrition; diet, PA; diet, PA, mental health) Reporting of intervention components and study quality varied greatly Mode Group/individual Telephone, newsletters Websites, postcards, booklet Duration 12 weeks (w)–1 year (y) Follow‐up time (FU) 12 weeks (w)–1 year (y) Comparator(s) UC |
Chasan‐Taber (27) Division of Biostatistics & Epidemiology, Dep. of Public Health, School of Public Health & Health Sciences, University of Massachusetts Amherst, MA, USA |
Quantitative RCTs n = 9 5 pilot Australia 4 USA 3 China 1 Malaysia 1 No quality assessment JBI 6 1,2,3,8,10,11 |
Women with previous GDM N = 1,386 |
Provide researchers and practitioners with a comprehensive overview of RCTs of lifestyle interventions designed to reduce the risk of DM or DM risk factors among women with a history of GDM |
Lifestyle interventions (diet, PA, breastfeeding) measured as impact on: T2DM incidence, weight, diet, PA, breastfeeding, and insulin resistance Weight (return to pre‐pregnancy weight if normal). 4/8 studies were conducted among women with current GDM or recent (within 2 m) Diet (healthy eating, low glycaemic index (GI), reduced calories, or <25/30% calories from fat) PA (moderate intensity) 150 min/w, 30 min/day for 3/5 times/w or 10,000 steps/day for 5 days/week Mode Group sessions/Individualized in‐person Telephone; Web‐based, text messaging, emails FU 10–12 months (m) Pilot studies 12 w ‐ 6 m Comparator Control arm or placebo |
Dasqupta 2018 (32) Centre for Outcomes Research and Evaluation (CORE), Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada |
Quantitative Invited core outcome set (COS) review Qualitative synthesis n = 16 Australia 6 USA 6 China 2 Ireland 1 Spain 1 Malaysia 2 Canada 1 No quality assessment JBI 8 1,2,3,4,5,8,10,11 |
Women with previous GDM N = 5194 7 studies did not specify population |
Gain insights on the factors that may enhance penetration and participation in Diabetes After Pregnancy prevention after GDM. Examine recruitment strategies and context |
The Health Behaviour Change (HBC) after pregnancy interventions varied: 2 focused on PA only, incorporating pedometers 4 adapted the US Diabetes Prevention Program (DPP) 5 PA, healthy eating and breastfeeding 1 followed the Finnish‐DPS curriculum, emphasis on a low‐fat diet 1 adopted Mediterranean diet type of approach 1 compared low‐fat to a low‐GI diet 1 incorporated group cooking lessons Mode face‐to‐face, group lessons telephone contact Web‐based |
Dennison 2019 (40) Primary Care Unit, Department of Public Health and Primary Care, Cambridge, UK |
Qualitative studies n = 21 Australia 7 Tonga 1 Canada 3 Sweden 3 USA 5 UK 1 Ireland 1 Denmark 1 CASP all studies 8/10 JBI 10 (all but 9) |
Women with previous GDM N = 903 |
Systematically synthesize the literature that focuses on the views of women with a history of GDM on reducing their risk of developing DM pp through lifestyle and behaviour changes. | Lifestyle and behaviour changes |
Feng 2018 (26) Departments of Nutrition and Nursing, Sir Run Shaw Hospital, School of Medicine Zhejiang University, Hangzhou, China |
Quantitative +MA n = 13 mn = 13 Prospective 6 Retrospective 7 USA 6, Ireland 1 Korea 2, Germany 1, Belgium 1, Australia 1, Italy1 New Castle‐Ottawa Scale PRISMA checklist JBI 10 1,2,3,4,5,6,7,8,9,11 |
Women with previous GDM N = 122,877 Sample size from 91–116,671 |
Investigate the association between lactation and development of type 2 DM in women with prior GDM. |
Breastfeeding Duration 4–12 week FU 6 weeks−19 years Comparator No breastfeeding Breastfeeding <2–3 w |
Gilinsky 2015 (27) School of Psychological & Health Sciences, UK |
Quantitative +MA n = 13 mn = 11 RCTs 10 RCT cross‐over 1 Pre‐post 2 USA 5 Australia 5 China 1 Hong Kong 1 Malaysia 1 RoB 3/13 rated as low bias risk. PRISMA checklist JBI 8 1,2,3,4,5,6,8,9 |
Women with previous GDM N = 1,960 |
Review lifestyle interventions for women with prior GDM to report study characteristics, intervention design and study quality and explore changes in
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Lifestyle PA and/or diet Breastfeeding Mode Face‐to‐face counselling Web‐based pedometer Telephone‐based education Group PA/education Electronic (SMS text/e‐mail) Newsletters Breastfeeding counselling 5‐day meal plan Free child care FU 6w−6y Comparator UC/no treatment Metformin and placebo Information on conventional dietary recommendations Written materials, two face‐to‐face education lessons (baseline, annually via phone/mail) Both groups advised to PA regularly (30 min, 3 times/w) Participants = own comparator |
Goveia 2018 (29) Postgraduate Program in Epidemiology, Universidad Federal do Rio Grande do Sul, Porto Alegre, Brazil |
Quantitative +MA n = 15 mn = 8 RCTs 15 USA 3, Australia 4, China 4, Spain 1, Malaysia 1, Israel 1, Ireland 1 RoB PRISMA checklist JBI 11 |
Women with previous GDM N = 2730 |
Compared lifestyle interventions: diet, PA or breastfeeding pp with UC without pharmacological treatment |
Lifestyle interventions focused on changes in diet and PA. 3 only PA, 1 only on diet, 1 only on breastfeeding Mode 9 remote contact (phone, Internet, or postcards) 4 group sessions 11 individual face‐to‐face sessions (2 of these home visits, 9 held in the clinic). Duration Varied FU 3 m−7 years Comparator Standard/brief advice on diet and/or PA |
Guo 2016 (30) School of Nursing, Central South University, Changsha, China. |
Quantitative n = 12 6 pilot/feasibility RCTs 12 Australia 4 USA 3 China 4 Malaysia 1 The Cochrane RoB Methodological rigour of included studies PRISMA checklist JBI 10 1,2,3,4,5,6,7,8,10, 11 |
Women with previous GDM N = 2757 8: pp women with impaired glucose tolerance /impaired FBG or insufficient PA 10: pp women (4: 6 w pp 1: 2 y pp 4: 3 y pp 1: 4 y pp 2) |
Systematically examine the components and effectiveness of pp lifestyle interventions in preventing T2DM in women with prior GDM Explore components of interventions that demonstrated a moderate effect on related measures of type 2 DM, insulin resistance, and weight. |
Lifestyle interventions Mode PA (1 individual counselling +pedometer+ 5 telephone contacts +7 postcards) PA and psychosocial support (13 sessions, education, pedometer messaging, Internet forum) Diet (1 individual low‐GI diet education +2 handouts) (3 m sessions +dietary advice sheet reminders of PA) Diet and PA (8 individual meetings +2 tel. contacts) (6 home visits+3 tel. contacts) (7 individual sessions) Diet, PA, and psychosocial support (4 individual/tel. sessions) (self‐help booklet+10 tel. sessions) Diet, PA, and breastfeeding (6 tel.+ 2 individual+8 optional tel. sessions+3 tel. contacts) Diet, PA, and behaviour modification (16 individual meetings+3 group sessions) Duration 12 weeks−36 months (median 6 months). FU 3–69 months Comparator Basic advice, written lifestyle recommendations, infant safety, and general health Conventional healthy dietary recommendation. Standard dietary advice sheet and reminding of need for PA Health education materials Oral information about awareness of DM |
Jones 2017 (18) Department of Nursing, College of Nursing and Health Sciences, University of Massachusetts Boston, USA |
Quantitative studies RCTs n = 10 2 = protocols, no findings USA 5 Australian 4 Canada 1 The Cochrane Collaboration RoB JBI 8 1,2,3,4,5,6,10,11 |
Women with previous GDM N = 520 N = 3,140 incl. protocols |
Synthesize current knowledge and practices around tailoring multimodal interventions for situational and cultural relevance to reduce type 2 DM risk in women with prior GDM. |
Multimodal home‐based lifestyle modification intervention Theoretical framework/underpinning interventions 4/8 Social cognitive theory 2/8 Trans theoretical model 4/8 No specific theory reported; relevant constructs: self‐efficacy, risk perception, perceived benefits and barriers, health beliefs, self‐regulation, behavioural goals, social support, barriers to change Mode 7 Motivational interviewing or patient‐cantered counselling with experts 6 tel., 5 supplementary face‐to‐face sessions 4 mailings, 3 website, 2 supplementary text messages Duration Interventions are divided into 3 distinct phases: Prenatal (3‐trimester; 10‐14w) Early pp (6 weeks−6 months) Late pp (6–12 months) FU 3–12 months Comparator UC |
Kaiser 2013 (35) Midwifery. University of Applied Sciences, Geneva, Switzerland |
Mixed n = 18 Cross‐sectional surveys = 10 Cross‐sectional, and interviews = 8 Australia 8, Canada 2, USA 7, Sweden 1 No quality assessment JBI 9 1,2,3,4,5,6,7,10,11 |
Women with GDM N = 19847 Sample sizes 10–17,742 |
To describe the most significant findings of the studies that examined the prevalence and determinants of pp health behaviours (PA, dietary habits and/or weight loss) in patients with GDM |
Identify factors that may impact the adherence to health behaviours specific for GDM patients What are the determinants of adherence or not to adequate pp health behaviours (PA, dietary habits, weight loss) and their potential determinants after GDM. Mode N/A Duration N/A FU 4 weeks−5 years |
Middleton 2014 (31) Australian Research Centre for Health of Women and Babies, New Zealand |
Cochrane review n = 1 RCT The Cochrane guideline GRADE JBI 10 1,2,3,4,5,6,7,9,10, 11 |
Women with a diagnosis of GDM in the index pregnancy. N = 256 |
To assess the effects of reminder systems to increase uptake of testing for T2DM or impaired glucose tolerance in women with a history of GDM. |
Reminders of any modality (post, email, phone (direct call or short SMS text) to either women with a history of GDM or their health professional, or both. Mode 3 m pp postal reminders 1) to the woman only, 2) to the physician only, 3) to both. Women and physicians were contacted 3 times during 1 y FU Duration 1 y FU 1 y Comparator No reminder |
Morton 2014 (25) Women's Health Research Unit London, UK |
Mixed studies n = 11 RCTs 6 Observational 5 RoB JBI 9 1,2,3,4,5,6,7,10,11 |
Women with GDM. N = 10,968 |
Assess the effectiveness of various interventions that delay or arrest the progression from GDM to T2DM. |
PA and/or dietary recommendation Breastfeeding Pharmacological interventions – Metformin Troglitazone 200 or 400 mg Pioglitazone 45 mg/day for 3 years Mode Advice by telephone, Individual counselling, lessons Recommendation Monitoring Food‐frequency questionnaire on DM by 14 years Questionnaires to calculate weekly energy expended in metabolic equivalent hours Duration FU 12 weeks−16 years Comparator No control/No intervention/ Placebo No breastfeeding (Ziegler)/ Women without GDM (Ratner) Routine advice on diet and PA plus low glycaemic dietary advice (Shyam) Alternate (Mediterranean) diet, approaches to hypertension (DASH) and healthy eating index (Tobias) Intensive advice diet, PA 3 m tel routine advice (Wein) |
Nielsen 2014 (36) Department of International Health, Immunology and Microbiology, University of Copenhagen, Denmark |
Mixed n = 58 RCTs, cohort, cross‐sectional, and qualitative studies Majority from high‐income countries: USA 28 Canada 8 Australia 10 New Zealand 1 Europe 7 No quality assessment JBI 5 1,2,5,10,11 |
Women with GDM N = 82,556 (1,053,345) N = 82,283 36 studies focusing on pp FU. (N = 273 15 studies focusing on GDM treatment) (N = 970,789 12 studies focusing on screening) |
Investigate determinants and barriers to GDM care from initial screening and diagnosis to prenatal treatment and pp FU. |
Screening during pregnancy Treatment of GDM during pregnancy and pp FU Healthy pp lifestyle interventions (diet or exercise) |
Peacock 2014 (37) School of Nursing and Midwifery, Faculty of Health Sciences, The University of Queensland, Australia |
Mixed quantitative/qualitative studies n = 30 RCTs 8 Observational 5 Cross‐sectional 8 Qualitative: Thematic Descriptive interpretive Modified grounded theory USA 11 Australia 11 Canada 2 Spain 1 Denmark 1 CONSORT (quality assessment of RCTs) JBI 9 1,2,3,4,5,6,8,10,11 |
Women previously diagnosed with GDM N = 184,502 Sample size: 10–177,420 |
Identify effective strategies and programmes to decrease the risk of T2DM in women who experience GDM, the barriers to participation, and the opportunities for midwives to assist women in prevention | Behavioural and pharmacological interventions intended to reduce maternal risk of T2DM |
Pedersen 2017 (20) Public Health, Section for Health Promotion and Health Services, Aarhus University, Denmark |
Quantitative +MA n = 10 RCTs = 9 Cluster RCT = 1, (44 medical centres, N = 2280) mn = 4 (951) Narrative synthesis Australia 4 USA 3 Asia 2 Europa 1 No quality assessment tool PRISMA checklist JBI 8 1,2,3,4,6,7,10,11 |
Women with a GDM diagnosis in the last pregnancy N = 3636 |
Review the evidence of effective behavioural interventions seeking to prevent T2DM |
T2DM preventive health behaviours among women with previous GDM Behavioural interventions implemented within 2 years of the pp period PA +diet 5 trials measured effect on DM incidence FU 1y – approximately 4y |
Tanase‐Nakao 2018 (33) Division of Maternal Medicine, Center for Maternal Foetal, Neonatal and Reproductive Medicine, Japan |
Quantitative n = 9 Observational: 3 prospective cohort 4 cross‐sectional 2 retrospective cohorts (case control) USA 7 Germany 1 Korea 1 Data synthesis conducted by random‐effect MA Risk of Bias Assessment tool for non‐randomized studies (RoBANS) MOOSE guidelines JBI 9 1,2,3,4,5,6,7,8,9 |
Women with previous GDM N = 3,699 |
Review current findings on breastfeeding for type 2 DM prevention |
Breastfeeding Duration FU 4 weeks – 5 years |
Van den Heuvel 2018 (38) Division of Woman and Baby, University Medical Center Utrecht Netherlands |
Mixed Narrative overview of the literature n = 71 No quality assessment JBI 6 1,2,3,7,10,11 |
Women prenatal, peri‐, and post‐ care | Provide a comprehensive and contemporary overview of the literature on eHealth in perinatal care and assess the applicability, advantages, limitations, and future of this new generation of pregnancy care |
Electronic health (eHealth) including Web‐based informative programs, remote monitoring, tele‐consultation, and mobile device–supported care Mode eHealth, telemedicine |
Van Ryswyk 2015 (39) Robinson Research Institute, The University of Adelaide, Australia |
Mixed n = 42 Survey‐only 15 Interviews 18 Interviews and surveys 4 Interviews and focus groups 3 Focus groups 2 United States 12 Australia 10, Europe/UK 9 Canada 7 Brazil 2 Vietnam 1 Tonga 1 CASP PRISMA checklist JBI 9 1,2,3,4,5,6,7,10,11 |
Women with previous GDM N = 7,949 |
Identify factors that influence pp healthcare seeking for women who have experienced GDM through synthesis of results from qualitative and survey studies |
Abbreviations: BMI, body mass index; CASP, Critical Appraisal Skills Programme; COS, core outcome set; DM, diabetes mellitus; FBG, Fasting Blood Glucose; FU, follow‐up; GDM, gestational diabetes; GI, glycaemic index; m, month; JBI, Joanna Briggs Institute; MA, meta‐analysis; NS, not significant; OGTT, oral glucose tolerance test; PA, physical activity; pp, postpartum; PRISMA, Preferred Reporting Items for Systematic Reviews and Meta‐analyses; RoB, Cochrane collaborations Risk of Bias Tool; RoBANS, Risk of Bias assessment tool for non‐randomized studies; RCT, randomized controlled trial; UC, usual care; w, week; y, year.