The Impact of Antenatal Psychological Group Interventions on Psychological Well-Being: A Systematic Review of the Qualitative and Quantitative Evidence
Abstract
:1. Introduction
1.1. Background
1.2. The Theoretical Bases of Interventions
2. Materials and Methods
2.1. Search Strategy
2.2. Inclusion and Exclusion Criteria
2.3. Data Extraction
2.4. Quality Assessment
3. Results
3.1. Identified Studies
3.2. Interventions
3.2.1. Psychological Approaches
3.2.2. Intervention Formats
3.3. Study and Participant Characteristics
3.3.1. Study Characteristics
3.3.2. Participant Characteristics
3.4. Quantitative Studies: Findings
3.4.1. Depressive Symptoms
3.4.2. Depressive Episodes
3.4.3. Anxiety
3.4.4. Stress
3.4.5. Potential Negative Effects of Interventions
3.4.6. Impact of Participant Characteristics
3.4.7. Impact of Intervention Characteristics
3.5. Findings from the Thematic Synthesis of Qualitative Studies
3.5.1. Qualitative Approaches
3.5.2. Analytical Themes
Connecting
“At the “project”, they understood me … I found a family with the people from the project and I liked that a lot. But I couldn’t have done it differently because I felt comfortable with those women [61].” “A lot of the meetings was about making friends, I’ve got a busy life, now if I feel I’m not good at anything we can just ring each other [37].” “It was great being around women who were in a similar situation to me and I liked being able to talk about my own experience [58].” “… the small and large group discussions … provided an opportunity to connect and relate to other women in the programme [58].”
Sharing
“Listening to them made us feel important … that was important … because like I always say, some people may be in the same situation as me [61].” “Sharing experiences and realising that they were not alone in what they felt (especially when these were negative feelings) helped women to normalise their experiences; in this way the course acted as a normalising catalyst [38].” “Being able to talk to someone and listen to advice [61].” “I learned that this is a shared human experience, and I’m not the only one who suffers [58].”
Understanding
“I have learned how to better understand my thoughts and my body. How my thoughts can trigger feelings and how these thoughts are not always factual [58].” “I became aware of my mood and I realised that what I had was not something bad … what I really had was low self-esteem [61].” “Yeah, that was fine, it was good, learning things, you know, social support, turning it down, asking for help … [37].”
Re-Adjusting and Normalising
“This is something that happens to women, after being involved in the project, it became more real to me [61].” “Being more accepting of myself, being more gentle to oneself, appreciating self-kindness, accepting anxiety as part of who I am, accepting my thoughts [58].” “Whenever I feel sad or depressed, I try to think about something nice, something that makes me feel happy, I learned all that there [61].”
4. Discussion
4.1. Interventions
4.2. Heterogeneity and Methodological Limitations
4.3. Effectiveness of Interventions
4.4. Women’s Experiences
4.4.1. Qualitative Studies
4.4.2. Women’s Feedback in Quantitative Studies
4.5. Combining Qualitative and Quantitaive
4.6. Strengths and Limitations of This Review
5. Conclusions
Acknowledgments
Conflicts of Interest
Abbreviations
BDI | Beck Depression Inventory |
CASP | Critical Appraisal Skills Programme |
CBT | Cognitive Behavioural Therapy |
CES-D | Centre for Epidemiologic Studies Depression scale |
EPDS | Edinburgh Postnatal Depression Scale |
IPT | Interpersonal Therapy |
MFN | Mindfulness |
NICE | National Institute for Health and Care Excellence |
PMI | Perinatal Mental Illness |
PND | Postnatal Depression |
PSS | Perceived Stress Scale |
STAI | Spielberger State-Trait Anxiety Inventory |
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Intervention | Participants | Study Design |
---|---|---|
Quantitative Studies | ||
Austin et al. 2008 (Australia) [23] | ||
Brief CBT intervention Aims: preventing/managing stress, anxiety and low mood Length: 12 h (6 × 2 h) Group size: no information Additional: information booklet, follow-up session Facilitator: clinical psychologist, midwife Evaluation/monitoring: no information | 277 women with depression/anxiety symptoms or at risk of depression/anxiety Characteristics: mean age 31 years; 97.8% partnered; 9.7% low income; 88.1% English speaking; 65.3% first child Mean 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 booklet Screening: EPDS > 10/ANRQ > 23/history of depression 1 Allocation: randomisation on 2:1 basis (intervention:control) after screening; concealment unclear Outcome measures: depression (MINI), depressive symptoms (EPDS), anxiety (STAI, MINI) Time points: pre-/post-intervention; 2 and 4 months postnatal Attrition/participation 2: high attrition, low participation Quality 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-based Aims: increased awareness of ongoing emotions, thoughts and behaviours Length: 12 h (8 × 90 min) Group size: 4–6 Factilitator: clinical psychologist Evaluation/monitoring: participant feedback | 160 women with elevated depressive/anxiety symptoms 4 Characteristics: mean age 29.5 years; 100% partnered; medium/high socio-economic status; 64.9% first child Mean gestational age: 16.4 weeks Baseline symptoms: STAI 38; EPDS: 7.4 (int), 5.9 (con) | RCT; control: usual care Screening: PDQ > 14 / STAI > 36 / BDI-S > 20 Allocation: random; concealed Outcome 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 postnatal Attrition/participation: high attrition, low participation Quality 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 psychoeducation Aims: Preventing PND Length: 12 h (6 × 2 h) Group size: 8–16 Additional: introductory meeting, PN reunion; one session with partners Facilitator: nurses, occupational therapists Evaluation/montitoring: participant feedback; supervision | 209 women at increased risk of depression Characteristics: median age 19 years; 73% European, others mostly Asian; 100% first child Gestational age: >28 weeks Baseline symptoms: GHQ-D high: 22/23% | RCT; control: usual care Screening: “Pregnancy and You“ screening questionnaire 5; 12–20 weeks Allocation: randomisation after screening (stratification based on 3 diagnostic factors); concealed Outcome measures: depression (SCAN), depressive symptoms (modified GHQ-D, EPDS); various risk factors for PND Time points: pre-intervention; 3 months postnatal Attrition/participation: low attrition, low participation Quality 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-based Aims: preventing PND Length: 6 h (4 × 90 min) Group size: no information Additional: individual PN booster session Facilitator: counsellors Evaluation/monitoring: participant feedback; audiotaping for adherence/supervision | 36 low-income African-American women, at risk of PND Characteristics: mean age 23.4 years; 13.9% partnered; mostly rural, low-income; 100% African American; 61.1% first child Gestational age range: 24–31 weeks Baseline symptoms: CSQ: mean score 34.5 6, no reported previous depressive episodes | Pilot RCT; control: usual care Screening: CSQ ≥ 27 Allocation: 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 postnatally Attrition/participation: medium attrition, high participation Quality 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 stress Length: 12 h (6 × 2 h) Group size: no information Facilitator: no information Evaluation/monitoring: no information | 47 women with raised stress and/or anxiety Characteristics: mean age 33.1 years; 93.5% partnered; medium-high socio-economic status; 66% white; 78% first child Gestational age range: 10–25 weeks Baseline 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 > 11 Allocation: randomisation (computerised) after screening; concealment unclear Outcome measures: perceived stress (PSS), pregnancy-specific anxiety (PSA), pregnancy-related anxiety (PRA), anxiety (STAI), mindfulness (FFMQ) Time points: pre-/post-intervention; 6 weeks after intervention Attrition/participation: medium attrition, medium participation Quality 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 partners Aims: preventing PND Length: 12 h (4 × 3 h) Group size: <15 Facilitator: psychiatrists and health visitors Evaluation/monitoring: sessions recorded randomly checked for adherence | 1719 women Characteristics: mean age 27 years; 66% partnered; 14% low-income; 61% first child Gestational age: >25 weeks Baseline symptoms: antenatal depression 18.4%; history of major depression 5.6% | RCT; control: routine antenatal course Screening: none (but subgroup analysis) Allocation: randomisation (computerised) after eligibility criteria met, on ¾:1 (intervention:control) basis; concealment unclear Outcome measures: depression (LQ > 11), depressive symptoms (LQ); questionnaire on various risk factors of PND Time points: pre-intervention; 6-8 weeks postnatal Attrition/participation: low attrition, no information on participation Quality 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-based Aims: preventing PND Length: 16 h (8 × 2 h) Group size: 5–10 Additional: 2 PN individual booster sessions; self-help book on depression (also for control) Facilitator: no information Evaluation/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 child Mean 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 care Screening: CES-D ≥ 16 / self-reported history of depression 7 Allocation: randomisation (block), before or after screening (see “quality assessment“); concealment unclear Outcome measures: depression (SCID), depressive symptoms (BDI-II), anxiety (SCL-90) Time points: baseline; 6 weeks and 4–6 months postnatal Attrition/participation: high attrition, low participation Quality 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 managrement Aims: preventing depression Format: 16 h (8 × 2 h) Group size: no information Additional: 3 individual PN booster sessions Facilitator: researchers Evaluation/monitoring: sessions filmed and selectively reviewed; supervision | 217 low-income women at high risk of depression Characteristics: 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 child Mean gestational age: ≤24 weeks at baseline Baseline symptoms: BDI-II 15.7 int, 14.9 con, BDI-II ≥ 20 25% int, 24% con | RCT; control: usual care Screening: CES-D ≥ 16 / self-reported personal or family history Allocation: randomization (sealed envelope) after screening; concealed Outcome measures: depressive symptoms (BDI-II), major depressive episodes (MS) Time points: pre-/post-intervention; 6 weeks, 4 and 12 months PN Attrition/participation: high attrition, low participation Quality 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-based Aims: reducing stress and depressive symptoms, enhancing happiness and self-efficacy in managing conflict Length: 6 h (4 × 90 min) Group size: no information Facilitator: no information Evaluation/monitoring: sessions video taped and reviewed | 156 women Characteristics: mean age 31.2 years; 91.8% partnered; 73.5% first child Mean gestational age: 20 weeks Baseline symptoms: EPDS > 12 41% (int) / 30% (con) | Multisite RCT; control: usual care Screening: none (but subgroup analysis) Allocation: permuted block randomisation (sub-sets of four) after eligibility established; concealed Outcome 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 postnatal Attrition/participation: low attrition, high participation Quality 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 managrement Aims: preventing depression Length: 24 h (12 × 2 h) Group size: 3–8 Additional: 4 PN booster sessions Facilitator: researchers Evaluation/monitoring: sessions filmed and reviewed, supervision | 41 women at high risk of depression Characteristics: mean age 24.9 years; 71.4% (int) / 80% (con) partnered; mostly low-income; 70% born in Mexico and Central America Mean gestational age: 16.1 (int) / 15.7 (con) weeks Baseline symptoms: CES-D 16.0 (int) / 16.8 (con); history of MDE 47.6% (int) / 60% (con) | RCT; control: usual care Screening: CES-D ≥ 16 / past history of major depressive episode (MMS) Allocation: randomisation after screening; method and concealment unclear Outcome measures: depression (MMS), depressive symptoms (CES-D, EPDS) Time points: pre-/post-intervention; 1, 3, 6 and 12 months postnatal Attrition/participation: low attrition, low participation Quality 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 5 See Bittner et al. 2014 [35] for further details | RCT; control: usual care Screening: PDQ > 14 / STAI > 36 / BDI-S > 20; 10–15 weeks Allocation: random (random allocation sequences); concealed Outcome measures: stress (PDQ, PSS), salivary cortisol Time points: pre-/post-intervention; 3 months postnatal Attrition/participation: high attrition, low participation Quality 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 depression Characteristics: mean age 25.4 years; >72% partnered; mostly low-income; >75% born in Mexico and Central America; mostly second or subsequent child Mean 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 risk Screening: CES-D ≥ 16 / past history of major depressive episode (MMS) Allocation: randomization after screening; method and concealment Outcome 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 postnatal Attrition/participation: low attrition, low participation Quality 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 Reduction Aims: reducing stress and improving mood Length: 16 h (8 × 2 h) Group size: no information Additional: CD with guided meditations Facilitator: clinical psychologist Evaluation/monitoring: no information | 31 women, with “mood concerns“ Characteristics: mean age 33.9 years; 100% partnered; medium-high socio-economic status; 74% white Mean gestational age: 25 weeks Baseline 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 clear Outcome 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-intervention Attrition/participation: low attrition, high participation Quality 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-based Aims: preventing PND Length: 4 h (4 × 1 h) Group size: no information Facilitator: no information Evaluation/monitoring: no information | 37 women on public assistance at risk of PND Characteristics: mean age 23.4 years; 23% partnered; low-income; 45% Caucasian Gestational age range: 20–32 weeks Baseline symptoms: BDI > 10: 70% int, 44% con; history of depression: 70% int, 51% con | Pilot RCT; control: usual care Screening: at least 1 predictor for risk factors for PND 8 Allocation: randomisation after screening; method and concealment unclear Outcome measures: depressive symptoms (BDI), depression (SCID) Time points: pre-/post-intervention; 3 months postnatal Attrition/participation: low attrition, high participation Quality 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-based Aims: preventing PND Length: 4 h (4 × 1 h) Group size: 3–5 Additional: individual PN booster Facilitator: nurses Evaluation/monitoring: no information | 99 women at risk of PND Characteristics: mean age 22.4 years; 33.3% partnered; low-income; 44% Hispanic Gestational age range: 23–32 weeks Baseline symptoms: previous MDE 31.3%; BDI 15.6 | RCT; control: usual care Screening: CSQ ≥ 27 Allocation: randomisation after screening (stratified for previous episode of depression); concealment unclear Outcome measures: depressive symptoms (BDI), depression (LIFE depression module), social adjustment (RIFT) Time points: pre-intervention; 3 months postnatal Attrition/participation: low attrition, medium participation Quality 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 anxiety Aims: coping with anxiety Format: 16 h (8 × 2 h) Group size: 6–12 Additional: MP3s of meditations for home practice Facilitator: clinical social worker Evaluation/monitoring: audiotaped and reviewed for fidelity and supervision | 24 women with elevated anxiety symptoms and no greater than moderate levels of depression Characteristics: mean age 33.5 years; 96% partnered; 75% white/non-Hispanic; 66.6% first child Mean gestational age: 15.5; range: 6–27 weeks Baseline symptoms: 70.8% met criteria for GAD | Qualitative content analysis Screening: PSWQ ≥ 45 / GAD-7 ≥ 10 / BAI ≥ 11 / PHQ-9 < 15 Data collection: written response to open-ended questions Attrition/participation: low attrition, high participation Quality 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 managrement Aims: preventing depression Format: 16 h (8 × 2 h) Group size: no information Additional: 3 individual PN booster sessions Facilitator: researchers Evaluation/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 immigrants Mean gestational age: no information Baseline symptoms: CES-D ≥ 16 23.1%; personal history of depression 69.4% | Inductive comparative analysis Screening: CES-D ≥ 16 / past history of major depressive episode (MMS) Data collection: semi-structured interviews Attrition/participation: low attrition, low participation Quality 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 child Gestational age: >28 weeks Baseline symptoms: unable to determine | Grounded theory Screening: “Pregnancy and You“ screening questionnaire 5; 12–20 weeks Data collection: interviews Attrition/participation: low attrition, low participation Quality 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) |
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Wadephul, F.; Jones, C.; Jomeen, J. The Impact of Antenatal Psychological Group Interventions on Psychological Well-Being: A Systematic Review of the Qualitative and Quantitative Evidence. Healthcare 2016, 4, 32. https://doi.org/10.3390/healthcare4020032
Wadephul F, Jones C, Jomeen J. The Impact of Antenatal Psychological Group Interventions on Psychological Well-Being: A Systematic Review of the Qualitative and Quantitative Evidence. Healthcare. 2016; 4(2):32. https://doi.org/10.3390/healthcare4020032
Chicago/Turabian StyleWadephul, Franziska, Catriona Jones, and Julie Jomeen. 2016. "The Impact of Antenatal Psychological Group Interventions on Psychological Well-Being: A Systematic Review of the Qualitative and Quantitative Evidence" Healthcare 4, no. 2: 32. https://doi.org/10.3390/healthcare4020032
APA StyleWadephul, F., Jones, C., & Jomeen, J. (2016). The Impact of Antenatal Psychological Group Interventions on Psychological Well-Being: A Systematic Review of the Qualitative and Quantitative Evidence. Healthcare, 4(2), 32. https://doi.org/10.3390/healthcare4020032