| Austin et al. 2008 (Australia) [23] |
| Brief CBT interventionAims: preventing/managing stress, anxiety and low moodLength: 12 h (6 × 2 h)Group size: no informationAdditional: information booklet, follow-up sessionFacilitator: clinical psychologist, midwifeEvaluation/monitoring: no information | 277 women with depression/anxiety symptoms or at risk of depression/anxietyCharacteristics: mean age 31 years; 97.8% partnered; 9.7% low income; 88.1% English speaking; 65.3% first childMean gestational age: 25.7 weeks (range: 14 to 36 weeks)Baseline symptoms: MINI: depression 19.1%, anxiety 26%, depression or anxiety 32.5%; EPDS > 12 14.3% of completers | RCT; control: information bookletScreening: EPDS > 10/ANRQ > 23/history of depression 1Allocation: randomisation on 2:1 basis (intervention:control) after screening; concealment unclearOutcome measures: depression (MINI), depressive symptoms (EPDS), anxiety (STAI, MINI)Time points: pre-/post-intervention; 2 and 4 months postnatalAttrition/participation 2: high attrition, low participationQuality assessment: B (differences in EPDS baseline scores; high rate attrition; wide range of gestational ages)Findings 3: No significant difference between groups (trend towards greater reduction in anxiety for intervention) |
| Bittner et al.
2014 (Germany) [35] |
| “LOS—Lebensfroh and optimistisch durch die Schwangerschaft“; CBT-basedAims: increased awareness of ongoing emotions, thoughts and behavioursLength: 12 h (8 × 90 min)Group size: 4–6Factilitator: clinical psychologistEvaluation/monitoring: participant feedback | 160 women with elevated depressive/anxiety symptoms 4Characteristics: mean age 29.5 years; 100% partnered; medium/high socio-economic status; 64.9% first childMean gestational age: 16.4 weeksBaseline symptoms: STAI 38; EPDS: 7.4 (int), 5.9 (con) | RCT; control: usual careScreening: PDQ > 14 / STAI > 36 / BDI-S > 20Allocation: random; concealedOutcome measures: depressive symptoms (EPDS), anxiety (STAI), dysfunctional attitudes (DAS), anxiety sensitivity (ASI), social support (SOZU), quality of relationship (PFB), fear of childbirth (GAS)Time points: pre-/post-intervention; 3 months postnatalAttrition/participation: high attrition, low participationQuality assessment: A (but high drop-out rate)Findings: no intervention effect on anxiety or depression; positive short-term effect on quality of relationship for intervention; women with elevated baseline depressive symptoms: significant decrease in depressive symptoms postnatally in intervention group |
| Brugha et al. 2000 (UK) [39] |
| “Preparing for Parenthood“; CBT elements and psychoeducationAims: Preventing PNDLength: 12 h (6 × 2 h)Group size: 8–16Additional: introductory meeting, PN reunion; one session with partnersFacilitator: nurses, occupational therapistsEvaluation/montitoring: participant feedback; supervision | 209 women at increased risk of depressionCharacteristics: median age 19 years; 73% European, others mostly Asian; 100% first childGestational age: >28 weeksBaseline symptoms: GHQ-D high: 22/23% | RCT; control: usual careScreening: “Pregnancy and You“ screening questionnaire 5; 12–20 weeksAllocation: randomisation after screening (stratification based on 3 diagnostic factors); concealedOutcome measures: depression (SCAN), depressive symptoms (modified GHQ-D, EPDS); various risk factors for PNDTime points: pre-intervention; 3 months postnatalAttrition/participation: low attrition, low participationQuality assessment: B (high attrition rates, insufficient detail on baseline comparisons)Findings: no intervention effect on levels of postnatal depression |
| Crockett et al. 2008 (US) [59] |
| “Reach Out, Stand Strong: Essentials for New Moms“ (ROSE) Program; IPT-basedAims: preventing PNDLength: 6 h (4 × 90 min)Group size: no informationAdditional: individual PN booster sessionFacilitator: counsellorsEvaluation/monitoring: participant feedback; audiotaping for adherence/supervision | 36 low-income African-American women, at risk of PNDCharacteristics: mean age 23.4 years; 13.9% partnered; mostly rural, low-income; 100% African American; 61.1% first childGestational age range: 24–31 weeksBaseline symptoms: CSQ: mean score 34.5 6, no reported previous depressive episodes | Pilot RCT; control: usual careScreening: CSQ ≥ 27Allocation: randomisation after screening; no further information Outcome measures: depressive symptoms (EPDS), PN adjustment (PPAQ), parenting stress (PSI)Time points: pre-/post-intervention; 2–3 weeks and 3 months postnatallyAttrition/participation: medium attrition, high participationQuality assessment: B (no information on allocation; results not presented comprehensively, small sample)Findings: significant increase in PN adjustment for intervention; no difference between groups in EPDS scores |
| Guardino et al. 2014 (US) [28] |
| Mindful Awareness Practices (MAPS) course at UCLA Semel Institute’s (ongoing course, not specifically for pregnancy)Aims: Reducing stressLength: 12 h (6 × 2 h)Group size: no informationFacilitator: no informationEvaluation/monitoring: no information | 47 women with raised stress and/or anxietyCharacteristics: mean age 33.1 years; 93.5% partnered; medium-high socio-economic status; 66% white; 78% first childGestational age range: 10–25 weeksBaseline symptoms: previous diagnosis of depression 30%; previous diagnosis of anxiety disorder 31%; STAI 45.7, PSS 41.8 | Pilot RCT; control: reading (pregnancy book)Screening: PSS > 34 / PSA > 11Allocation: randomisation (computerised) after screening; concealment unclearOutcome measures: perceived stress (PSS), pregnancy-specific anxiety (PSA), pregnancy-related anxiety (PRA), anxiety (STAI), mindfulness (FFMQ)Time points: pre-/post-intervention; 6 weeks after interventionAttrition/participation: medium attrition, medium participationQuality assessment: C (small sample; wide range of gestational ages; follow-up for some postnatally, others are possibly still pregnant) Findings: significantly larger decreases in pregnancy-specific anxiety pre- to post-intervention than control, not sustained at 6 weeks post-intervention |
| Kozinszky et al. 2012 (Hungary) [40] |
| CBT and IPT elements; including partnersAims: preventing PNDLength: 12 h (4 × 3 h)Group size: <15Facilitator: psychiatrists and health visitorsEvaluation/monitoring: sessions recorded randomly checked for adherence | 1719 womenCharacteristics: mean age 27 years; 66% partnered; 14% low-income; 61% first childGestational age: >25 weeksBaseline symptoms: antenatal depression 18.4%; history of major depression 5.6% | RCT; control: routine antenatal courseScreening: none (but subgroup analysis)Allocation: randomisation (computerised) after eligibility criteria met, on ¾:1 (intervention:control) basis; concealment unclearOutcome measures: depression (LQ > 11), depressive symptoms (LQ); questionnaire on various risk factors of PNDTime points: pre-intervention; 6-8 weeks postnatalAttrition/participation: low attrition, no information on participationQuality assessment: A (large sample; length of follow-up relatively short; no information on attendance rates)Findings: significantly reduced risk of PND and depressive symptoms in intervention group; women with AN depression: 17.8% risk reduction (without AND: 0.4%); intervention: significantly lower perceived lack of support from partner |
| Lara et al. 2010 (Mexico) [42] |
| “Salud Mental de Mamás y Bebés“; CBT-basedAims: preventing PNDLength: 16 h (8 × 2 h)Group size: 5–10Additional: 2 PN individual booster sessions; self-help book on depression (also for control)Facilitator: no informationEvaluation/monitoring: participant feedback; sessions filmed and reviewed | 377 women at high risk of depression Characteristics: mean age: 26.9 years; 85.7% partnered; low-middle socio-economic status; 25.5% first childMean gestational age: 26.9 weeks Baseline symptoms: major depression (SCID) 17.4%, BDI-II ≥ 14 62.7%, anxiety (SCL-90) 14.8% | RCT; control: usual careScreening: CES-D ≥ 16 / self-reported history of depression 7Allocation: randomisation (block), before or after screening (see “quality assessment“); concealment unclearOutcome measures: depression (SCID), depressive symptoms (BDI-II), anxiety (SCL-90)Time points: baseline; 6 weeks and 4–6 months postnatalAttrition/participation: high attrition, low participationQuality assessment: B (randomisation problematic: for 44% baseline interview took place before randomisation, for others after, resulting in significant differences in depressive symptoms: women who knew which group they had been randomised to reported higher CES-D scores; high attrition rate before start of intervention) Findings: significantly lower cumulative incidence of (new) major depression over all time points for intervention group; no intervention effect on depressive symptoms |
| Le et al. 2011 (US) [60] |
| “Mamás y Bebés / Mothers and Babies Course“; cognitive behavioural stress managrementAims: preventing depressionFormat: 16 h (8 × 2 h)Group size: no informationAdditional: 3 individual PN booster sessionsFacilitator: researchersEvaluation/monitoring: sessions filmed and selectively reviewed; supervision | 217 low-income women at high risk of depressionCharacteristics: mean age 25 years; 69.6% (int) / 57.1% (con) partnered; mostly low-income; mostly Central and South American immigrants; 38.4% (int) / 46.7% (con) first childMean gestational age: ≤24 weeks at baselineBaseline symptoms: BDI-II 15.7 int, 14.9 con, BDI-II ≥ 20 25% int, 24% con | RCT; control: usual careScreening: CES-D ≥ 16 / self-reported personal or family historyAllocation: randomization (sealed envelope) after screening; concealedOutcome measures: depressive symptoms (BDI-II), major depressive episodes (MS)Time points: pre-/post-intervention; 6 weeks, 4 and 12 months PNAttrition/participation: high attrition, low participationQuality assessment: C (low participation and high attrition; baseline comparatibility of groups problematic)Findings: significantly fewer depressive symptoms immediately post-intervention (small effect size); fewer cases of moderate depression (BDI-II ≥ 20) post-intervention; stronger size of effects for women who attended more session; no difference postnatally; no difference in cumulative incidence of major depressive episodes |
| Leung & Lam 2012 (China, Hong Kong) [41] |
| IPT-basedAims: reducing stress and depressive symptoms, enhancing happiness and self-efficacy in managing conflictLength: 6 h (4 × 90 min)Group size: no informationFacilitator: no informationEvaluation/monitoring: sessions video taped and reviewed | 156 womenCharacteristics: mean age 31.2 years; 91.8% partnered; 73.5% first child Mean gestational age: 20 weeksBaseline symptoms: EPDS > 12 41% (int) / 30% (con) | Multisite RCT; control: usual careScreening: none (but subgroup analysis)Allocation: permuted block randomisation (sub-sets of four) after eligibility established; concealedOutcome measures: stress (PSS), depressive symptoms (EPDS), happiness (SHS), self-efficacy in managing conflict (REM), perceived ability to cooperate (single question), perceived health (single question)Time points: pre-/post-intervention; 6–8 weeks postnatalAttrition/participation: low attrition, high participationQuality assessment: A (but intervention very culturally specific, focus on relationship with grandparents) Findings: significantly lower perceived stress (moderate effect size) and smaller decrease in happiness (small/moderate effect size) post-intervention, not sustained postnatally; women with depressive baseline symptoms: lower stress (moderate effect size) and smaller decrease in happiness post-intervention, increased relationship self-efficacy (large effect size); no difference in depressive symptoms |
| Muñoz et al. 2007 (US) [43] |
| “Mamás y Bebés / Mothers and Babies Course“; cognitive behavioural stress managrementAims: preventing depressionLength: 24 h (12 × 2 h)Group size: 3–8Additional: 4 PN booster sessionsFacilitator: researchersEvaluation/monitoring: sessions filmed and reviewed, supervision | 41 women at high risk of depressionCharacteristics: mean age 24.9 years; 71.4% (int) / 80% (con) partnered; mostly low-income; 70% born in Mexico and Central AmericaMean gestational age: 16.1 (int) / 15.7 (con) weeksBaseline symptoms: CES-D 16.0 (int) / 16.8 (con); history of MDE 47.6% (int) / 60% (con) | RCT; control: usual careScreening: CES-D ≥ 16 / past history of major depressive episode (MMS)Allocation: randomisation after screening; method and concealment unclearOutcome measures: depression (MMS), depressive symptoms (CES-D, EPDS)Time points: pre-/post-intervention; 1, 3, 6 and 12 months postnatalAttrition/participation: low attrition, low participationQuality assessment: B (no information on randomisation, relatively low attendance, no analysis of attenders/non-attenders; postnatal booster sessions may affect outcomes)Findings: no significant differences in depressive symptoms or incidence of MDEs |
| Richter et al. 2012 (Germany) [36] |
| See Bittner et al. 2014 [35] | 129 women with elevated stress, anxiety or depression 5See Bittner et al. 2014 [35] for further details | RCT; control: usual careScreening: PDQ > 14 / STAI > 36 / BDI-S > 20; 10–15 weeksAllocation: random (random allocation sequences); concealedOutcome measures: stress (PDQ, PSS), salivary cortisolTime points: pre-/post-intervention; 3 months postnatalAttrition/participation: high attrition, low participationQuality assessment: A (but high attrition) Findings: intervention: significant change in morning cortisol compared to control post-intervention but not postnatally; no significant difference in perceived stress |
| Urizar & Muñoz 2011 (US) [45] |
| See Muñoz et al. 2007 [43] | 86 women at-risk of depressionCharacteristics: mean age 25.4 years; >72% partnered; mostly low-income; >75% born in Mexico and Central America; mostly second or subsequent childMean gestational age: 16–17 weeks (range: 6–27 weeks)Baseline symptoms: CES-D 20.6 (int), 23.7 (con1), 9.4 (con2); history of MDE 33.3% (int), 66.% (con1), 0% (con2) | RCT; control 1: usual care, control 2: low riskScreening: CES-D ≥ 16 / past history of major depressive episode (MMS)Allocation: randomization after screening; method and concealmentOutcome measures: salivary cortisol levels (mother & infant), perceived stress, depressive symptoms (CES-D), depression (MMS), positive/negative affect (PANAS)Time points: baseline; 6 and 18 months postnatalAttrition/participation: low attrition, low participationQuality assessment: B (postnatal booster sessions may affect outcomes; large variation in gestational age)Findings: intervention and control 2: significantly lower infant cortisol levels at 6 months PN; intervention: lower maternal cortisol levels than control 1 at 18 months PN; significantly higher levels of perceived stress at 6 months PN in intervention group |
| Vieten & Astin 2008 (US) [46] |
| “Mindful Motherhood“, based on Mindfulness-Based Stress ReductionAims: reducing stress and improving moodLength: 16 h (8 × 2 h)Group size: no informationAdditional: CD with guided meditationsFacilitator: clinical psychologistEvaluation/monitoring: no information | 31 women, with “mood concerns“Characteristics: mean age 33.9 years; 100% partnered; medium-high socio-economic status; 74% whiteMean gestational age: 25 weeksBaseline symptoms: perceived stress 20.1 int, 17.1 con; state anxiety 43.8 int, 35.6 con; CES-D 20.4 int, 14.2 con | Pilot RCT; control: wait-list control (postnatal)Screening: positive response to “Have you had a history of mood concerns for which you sought some form of treatment…?“Allocation: randomisation after screening; concealment not clearOutcome measures: perceived stress (PSS), positive/negative affect (PANAS), depressive symptoms (CES-D), anxiety (STAI), affect regulation (ARM), mindfulness (MAAS)Time points: pre-/post-intervention; 3 months post-interventionAttrition/participation: low attrition, high participationQuality assessment: C (no baseline comparisons between groups but there seem to be differences; no information on attenders / completers; follow-up at different times, postnatally or during pregnancy)Findings: significantly reduced state anxiety and negative affect with large effect sizes post-intervention compared to control, not sustained 3 months post-intervention |
| Zlotnick et al. 2001 (US) [61] |
| “Survival Skills for New Moms“; IPT-basedAims: preventing PNDLength: 4 h (4 × 1 h)Group size: no informationFacilitator: no informationEvaluation/monitoring: no information | 37 women on public assistance at risk of PNDCharacteristics: mean age 23.4 years; 23% partnered; low-income; 45% CaucasianGestational age range: 20–32 weeksBaseline symptoms: BDI > 10: 70% int, 44% con; history of depression: 70% int, 51% con | Pilot RCT; control: usual careScreening: at least 1 predictor for risk factors for PND 8Allocation: randomisation after screening; method and concealment unclearOutcome measures: depressive symptoms (BDI), depression (SCID)Time points: pre-/post-intervention; 3 months postnatalAttrition/participation: low attrition, high participationQuality assessment: C (limited details; short intervention; apparent differences at baseline between intervention and control; small sample)Findings: Intervention: women significantly less likely to develop PND |
| Zlotnick et al. 2006 (US) [44] |
| “Reach Out, Stand Strong: Essentials for New Moms“ (ROSE) Program; IPT-basedAims: preventing PNDLength: 4 h (4 × 1 h)Group size: 3–5Additional: individual PN boosterFacilitator: nursesEvaluation/monitoring: no information | 99 women at risk of PNDCharacteristics: mean age 22.4 years; 33.3% partnered; low-income; 44% HispanicGestational age range: 23–32 weeks Baseline symptoms: previous MDE 31.3%; BDI 15.6 | RCT; control: usual careScreening: CSQ ≥ 27Allocation: randomisation after screening (stratified for previous episode of depression); concealment unclearOutcome measures: depressive symptoms (BDI), depression (LIFE depression module), social adjustment (RIFT)Time points: pre-intervention; 3 months postnatalAttrition/participation: low attrition, medium participationQuality assessment: B (intervention relatively short, no measurement immediately after the intervention; no detailed description of the intervention)Findings: 3 months PN: fewer women in intervention with PND than in control (4% vs. 20%); no significant difference between groups for depression severity (BDI) or social adjustment at 3 months PN |
| Qualitative Studies |
| Goodman et al. 2014 (US) [58] |
| Coping with anxiety through Living Mindfully (CALM) Pregnancy; mindfulness-based cognitive therapy adapted for pregnant women with anxietyAims: coping with anxietyFormat: 16 h (8 × 2 h)Group size: 6–12Additional: MP3s of meditations for home practiceFacilitator: clinical social workerEvaluation/monitoring: audiotaped and reviewed for fidelity and supervision | 24 women with elevated anxiety symptoms and no greater than moderate levels of depressionCharacteristics: mean age 33.5 years; 96% partnered; 75% white/non-Hispanic; 66.6% first childMean gestational age: 15.5; range: 6–27 weeksBaseline symptoms: 70.8% met criteria for GAD | Qualitative content analysisScreening: PSWQ ≥ 45 / GAD-7 ≥ 10 / BAI ≥ 11 / PHQ-9 < 15Data collection: written response to open-ended questions Attrition/participation: low attrition, high participationQuality assessment: B (insufficient details of how study was explained to participants, insufficient details of data analysis; limited discussion regarding credibility of findings and value of research)Findings: seven categories: skill building; connection; universality; acceptance and self-kindness; decreased reactivity; cognitive changes; insight |
| Le et al. 2013 (US) [61] |
| “Mamás y Bebés / Mothers and Babies Course“; cognitive behavioural stress managrementAims: preventing depressionFormat: 16 h (8 × 2 h)Group size: no informationAdditional: 3 individual PN booster sessionsFacilitator: researchersEvaluation/monitoring: sessions filmed and selectively viewed | 39 women (participants in Le et al. 2011 [60])Characteristics: mean age 27.8 years; 61.5% partnered; mostly Central and South American immigrantsMean gestational age: no information Baseline symptoms: CES-D ≥ 16 23.1%; personal history of depression 69.4% | Inductive comparative analysisScreening: CES-D ≥ 16 / past history of major depressive episode (MMS)Data collection: semi-structured interviewsAttrition/participation: low attrition, low participationQuality assessment: B (lacking in detail about recruitment strategy, data collection, relationship between researcher and participants, data analysis)Findings: Women valued participating in the course; support network; awareness of mood; increased maternal efficacy; reduced isolation; child development; group experience; using tool |
| Wheatley & Brugha 1999 (UK) [37] |
| See Brugha et al. 2000 [39]; CBT-based | 9 women (subsample of Brugha et al. 2000 [39])Characteristics: mean age 25.6 years; 68.7% white; 100% first childGestational age: >28 weeksBaseline symptoms: unable to determine | Grounded theoryScreening: “Pregnancy and You“ screening questionnaire 5; 12–20 weeksData collection: interviewsAttrition/participation: low attrition, low participationQuality assessment: B (some detail lacking in how the study was explained to participants and data analysis; limited discussion regarding credibility of findings and value of research)Findings: themes: postnatal depression (lack of knowledge as protective or vulnerable); positive experience |
| Wheatley et al. 2003 (UK) [38] |
| See Brugha et al. 2000 [39]; CBT-based | See Wheatley & Brugha 1999 [37] | Grounded theory (focus on engagement with intervention)See Wheatley & Brugha 1999 [37]Quality assessment: B (no clear statement of the aim; lack of detail about aspects relating to the appropriateness of the recruitment strategy, data collection, consideration of the researcher/participant relationship, the ethical issues and data analysis)Findings: Themes: initial engagement (need for information about PND, PND taboo, decision-making, practicalities); maintaining engagement (sharing experiences, normalising, sensitivity of PND, positive experience, practicalities) |