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Efficacy of psychosocial interventions for survivors of intimate partner violence: protocol for a systematic review and meta-analysis

Published online by Cambridge University Press:  03 January 2023

Hannah M. Micklitz Open the ORCID record for Hannah M. Micklitz [Opens in a new window] ,
Carla M. Glass ,
Jürgen Bengel  and
Lasse B. Sander Open the ORCID record for Lasse B. Sander [Opens in a new window]
Hannah M. Micklitz*
Affiliation:
Department of Medical Psychology and Medical Sociology, Faculty of Medicine, University of Freiburg, Freiburg, Germany
Carla M. Glass
Affiliation:
Department of Rehabilitation Psychology and Psychotherapy, Institute of Psychology, University of Freiburg, Freiburg, Germany
Jürgen Bengel
Affiliation:
Department of Rehabilitation Psychology and Psychotherapy, Institute of Psychology, University of Freiburg, Freiburg, Germany
Lasse B. Sander
Affiliation:
Department of Medical Psychology and Medical Sociology, Faculty of Medicine, University of Freiburg, Freiburg, Germany
*
Correspondence: Hannah M. Micklitz. Email: [email protected]
Rights & Permissions [Opens in a new window]

Summary

Survivors of intimate partner violence (IPV) are at risk for serious health consequences, and providing effective psychosocial interventions to support these individuals is a major global health challenge. Previous systematic reviews and meta-analyses in this field do not allow for clear conclusions about the efficacy of these interventions, owing to a narrow focus on specific subpopulations or intervention formats. This protocol presents a systematic review and meta-analysis, which will provide a comprehensive overview of the empirical evidence of various psychosocial interventions for survivors of IPV and investigate their efficacy in improving safety-related, mental health and psychosocial outcomes both overall and within homogeneous subgroups (trial registration: https://osf.io/4gp95). We will systematically search the literature databases PsycInfo, MEDLINE, Embase and CENTRAL. Randomised controlled trials evaluating the efficacy of psychosocial interventions in increasing the safety or mental health of IPV survivors compared with a control group will be eligible. We will extract relevant data from eligible studies and assess study quality using the Cochrane Risk of Bias 2 (RoB 2) tool. We will qualitatively summarise the results and we will calculate weighted effect sizes under random effect model assumption for the primary outcomes IPV, depression and post-traumatic stress disorder. We will perform subgroup analyses to investigate the moderating effects of theoretical basis, delivery mode, intensity and setting of psychosocial interventions. The resultant overview of the current body of evidence for psychosocial interventions for IPV survivors is intended to inform future research and practice.

Keywords

Intimate partner violencedomestic violencepsychosocial interventionsmeta-analysisreview
Type
Paper
Information
BJPsych Open , Volume 9 , Issue 1 , January 2023 , e9
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Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
Copyright © The Author(s), 2022. Published by Cambridge University Press on behalf of the Royal College of Psychiatrists

Intimate partner violence (IPV) is a highly prevalent and global concern of public health and a major human rights violation. Globally, it is estimated that around 26% (95% CI 22–30%) of women have been subjected to physical and/or sexual violence from a current or former male intimate partner at some stage in their lives.1 IPV is considered the most widespread manifestation of violence against women,1 yet IPV affects people of all genders, regardless of sexual orientation or relationship type.Reference Laskey, Bates and Taylor2 Survivors of IPV are at an elevated risk for loss of home,Reference Daoud, Matheson, Pedersen, Hamilton-Wright, Minh and Zhang3 economic insecurity and unemploymentReference Showalter, Yoon and Logan4 and deterioration in quality of lifeReference Wathen, MacGregor and MacQuarrie5 and social functioning.Reference Bonomi, Thompson, Anderson, Reid, Carrell and Dimer6 Further, experiencing IPV increases the risk for numerous mental health conditions, including post-traumatic stress disorder (PTSD), depression, anxiety, substance misuse, pain syndromes, sleep disturbances and suicidality.Reference Bonomi, Thompson, Anderson, Reid, Carrell and Dimer6,Reference Bacchus, Ranganathan, Watts and Devries7 In its most severe form, IPV can escalate into intimate partner homicide.Reference Zara and Gino8

Effective and low threshold support services are urgently needed to improve the safety of IPV survivors and to reduce harms and negative consequences they face. For this purpose, a broad range of psychosocial interventions have been developed and implemented in healthcare and support systems worldwide.Reference Sprague, Woollett, Black and Hatcher9 These interventions include counselling, professional and peer support services, psychotherapy and more comprehensive programmes.Reference Niolon, Kearns, Dills, Rambo, Irving and Armstead10 Advocacy and cognitive–behavioural approaches are commonly used,Reference Condino, Tanzilli, Speranza and Lingiardi11,Reference García-Moreno, Hegarty, D'Oliveira, Koziol-McLain, Colombini and Feder12 sometimes integrated into a hybrid treatment model.Reference Eckhardt, Murphy, Whitaker, Sprunger, Dykstra and Woodard13 The psychosocial interventions can be short or long termReference Eckhardt, Murphy, Whitaker, Sprunger, Dykstra and Woodard13 and take place in primary care, crisis centres, shelters, in- and out-patient settings and in the community,Reference Bair-Merritt, Lewis-O'Connor, Goel, Amato, Ismailji and Jelley14 they can be delivered face-to-face individually, for couples or in groups,Reference Karakurt, Whiting, van Esch, Bolen and Calabrese15–Reference Tirado-Muñoz, Gilchrist, Farré, Hegarty and Torrens17 remote via telephone or video callsReference Anderson, McClelland, Krause, Krause, Garcia and Koss18,Reference Ogbe, Harmon, Van den Bergh and Degomme19 and online through internet and smartphone-based platforms and applications that contain human guidance in varying degrees.Reference Anderson, McClelland, Krause, Krause, Garcia and Koss18,Reference El Morr and Layal20,Reference Linde, Bakiewicz, Normann, Hansen, Lundh and Rasch21

Previous systematic reviews and meta-analyses found only scarce and inconsistent evidence on the efficacy of psychosocial interventions in preventing recurrence of IPV and reducing related health and psychosocial impairment of IPV survivors. Many authors have pointed out the poor quality of primary studies, mostly because of pre–post study design,Reference Rivas, Vigurs, Cameron and Yeo22 small samplesReference Trabold, McMahon, Alsobrooks, Whitney and Mittal23 and unreliable outcomes measures.Reference Linde, Bakiewicz, Normann, Hansen, Lundh and Rasch21,Reference Rivas, Vigurs, Cameron and Yeo22 However, the reviews and meta-analyses are also affected in their scope and reliability by methodological limitations. Most reviews and meta-analyses exclusively focus on specific subpopulations (e.g. pregnant women,Reference Howell, Miller-Graff, Hasselle and Scrafford24,Reference Cork, White, Noel and Bergin25 LGTBQ+ couplesReference Subirana-Malaret, Gahagan and Parker26), settings (e.g. during or after shelter,Reference Jonker, Sijbrandij, van Luijtelaar, Cuijpers and Wolf27 healthcare settingsReference Sprague, Woollett, Black and Hatcher9,Reference Bair-Merritt, Lewis-O'Connor, Goel, Amato, Ismailji and Jelley14,Reference Tarzia, Forsdike, Hegarty and Feder28 ), intervention formats (e.g. digital interventions,Reference Anderson, McClelland, Krause, Krause, Garcia and Koss18,Reference El Morr and Layal20,Reference Linde, Bakiewicz, Normann, Hansen, Lundh and Rasch21,Reference Eisenhut, Sauerborn, García-Moreno and Wild29 advocacy interventions,Reference Rivas, Vigurs, Cameron and Yeo22,Reference Rivas, Ramsay, Eldridge, Sadowski, Davidson and Dunne30 psychological interventionsReference Arroyo, Lundahl, Butters, Vanderloo and Wood16,Reference Hameed, O'Doherty, Gilchrist, Tirado-Muñoz, Taft and Chondros31 ) or outcomes (e.g. reduction of IPV,Reference Tirado-Muñoz, Gilchrist, Farré, Hegarty and Torrens17 social support and mental health outcomesReference Ogbe, Harmon, Van den Bergh and Degomme19). Although these approaches recognise the wide heterogeneity of existing psychosocial interventions, their use results in difficulties in interpreting the overall effectiveness and the comparative effectiveness across homogeneous subgroups. Moreover, it also impedes investigations into potential moderators of the effectiveness of psychosocial interventions for IPV survivors. Trabold and colleagues have attempted to address this challenge in a broad systematic review.Reference Trabold, McMahon, Alsobrooks, Whitney and Mittal23 However, it included only studies up to 2016 and did not perform meta-analytic pooling.

Therefore, in this protocol we present a systematic review and meta-analysis that will integrate a broad range of psychosocial interventions for survivors of IPV to achieve the following research objectives:

  1. (a) provide an up-to-date and comprehensive overview of psychosocial interventions for IPV survivors

  2. (b) perform meta-analyses investigating the efficacy of psychosocial interventions for survivors of IPV in terms of safety-related, mental health and psychosocial outcomes

  3. (c) perform subgroup analysis to reduce heterogeneity and to investigate potential effect moderators.

Method

The reporting of this protocol follows the Preferred Reporting Items for Systematic Review and Meta-Analysis Protocols (PRISMA-P) statement. We will report the systematic review and meta-analysis in accordance with Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. We preregistered the review in the Open Science Framework (OSF) database (https://osf.io/4gp95). We will list potential deviations from the study protocol in the final report.

Eligibility criteria

Studies will be selected based on the population, intervention, comparison, outcomes and study design (PICOS) criteria listed in the Appendix below. We will include studies published in a peer-reviewed journal, irrespective of publication date or language. If necessary, publications will be translated to English.

The target population consists of IPV survivors (i.e. people exposed to IPV prior to or at study baseline). Samples can include individuals or couples, but samples including only perpetrators are ineligible. Studies will qualify for inclusion if they investigate any psychosocial intervention that explicitly targets IPV or the mental health of IPV survivors, regardless of setting, delivery mode and duration. We will exclude studies that examine interventions for primary prevention (e.g. interventions targeting stigma, screening-only interventions), interventions aimed only at perpetrators or gatekeepers (e.g. family doctors, teachers), interventions that target exclusively associated symptoms (e.g. safe sex) or economic well-being (e.g. cash transfer), or provide physical safety or medical treatment only (e.g. shelter, emergency department). Studies with any comparison group (e.g. no treatment, waiting list, placebo, treatment as usual (TAU) or another treatment) are eligible. Studies need to report a quantitative measure related to IPV, mental health or psychosocial well-being. In terms of study design, only randomised controlled trials will be included. We will record study protocols to provide an overview on upcoming research.

Search strategy and selection process

We will systematically search the electronic databases PsycINFO (via EBSCO), Medline (via PubMed), Embase (via Ovid) and the Cochrane Central Register of Controlled Trials (CENTRAL). We will use a predefined search string, consisting of different medical subject headings (MeSH terms) and text words related to the key concepts of IPV, intervention/treatment and randomised controlled trial (RCT) (Supplementary Appendix A, available at https://dx.doi.org/10.1192/bjo.2022.625). We tested the sensitivity of the search string in a pilot search with a validation set of 25 relevant studies and obtained a coverage of 100%. References yielded by the systematic database search will be uploaded to the Cochrane toolkit Covidence.32 This software assists the selection and data collection process and thus improves accuracy of the procedure. After removal of duplicates, we will screen titles and abstracts. If the contained information indicates that studies are ineligible, they will be declined. Otherwise, full texts will be screened. Two reviewers (H.M.M., C.M.G.) will conduct this procedure independently. Divergent decisions about the inclusion of a study will be resolved via consensus discussion or by consultation with a third reviewer (L.B.S.). We will hand-search reference lists of selected articles (backward search) to identify eligible trials not detected by the electronic database searches. In addition, forward searches will be performed using the Google Scholar platform. We will use a PRISMA flowchart to illustrate the selection process and to specify reasons for study exclusion.

Ethics statement

No ethics approval will be needed as only data from previously published studies will be analysed.

Data items

We will extract the data using a predefined and piloted extraction sheet (Supplementary Appendix B). For each included study, the following items will be extracted from publications: (a) study identification items, (b) study design characteristics, (c) participant characteristics, (d) intervention characteristics, (e) control characteristics and (f) characteristics and results for safety-related, mental health, psychosocial, satisfaction, acceptance and treatment adherence outcomes. Data will be extracted by one researcher (C.M.G.) and double-checked by a second researcher (H.M.M.). A third researcher (L.B.S.) will be consulted in case of ambiguities.

Quality assessment

We will evaluate risk of bias using the Cochrane Risk of Bias 2 (RoB 2) tool for RCTs.Reference Deeks, Higgins, Altman, Higgins, Thomas, Chandler, Cumpston, Li and Page33 For each primary study we will assess bias in five domains: (1) bias arising from the randomisation process, (2) bias due to deviations from the intended interventions, (3) bias due to missing outcome data, (4) bias in measurement of the outcome, and (5) bias in selection of reported results. For domain 2, we will judge the ‘effect of the assignment to the intervention’. Based on judgement across these five domains, we will rate overall risk of bias. We will determine likelihood of publication bias by identification of study protocols and trial registrations. If the number of included studies is sufficient, publication bias will also be evaluated graphically by funnel plot and statistically by Egger's test of funnel plot asymmetry.Reference Sterne, Sutton, Ioannidis, Terrin, Jones and Lau34 Additionally, we will rate the quality of evidence for each primary outcome using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) guidelines.Reference Ryan and Hill35 The evaluation criteria are (a) risk of bias, (b) inconsistency, (c) indirectness, (d) imprecision and (e) publication bias. Two reviewers (C.M.G., H.M.M.) will independently perform the quality assessment. Any deviations will be resolved by discussion; if needed, a third reviewer (L.B.S.) will be included.

Data synthesis

Qualitative synthesis

We will conduct a narrative synthesis of all included studies. We will report characteristics and results (see ‘Data items’ above) of each included study in both text and tables. We will summarise study protocols and report ongoing research in the field.

Meta-analysis

We will calculate between-group effect sizes (Hedges’ g and standard error) for each included study using post-intervention scores (i.e. first measurement of outcomes after treatment exposure) for the intervention and control groups. Additionally, we will use available follow-up scores to examine whether the effects persist at medium-term follow-up (i.e. 6–11 months post baseline) and long-term follow-up (i.e. ≥12 months post baseline).

We will perform meta-analyses calculating pooled between-group effect sizes (Hedges’ g with 95% confidence intervals for continuous outcomes or odds ratio for dichotomous outcomes) for psychosocial interventions compared with control conditions for each outcome in a random effects model. Weighting of studies will be based on inverse variance. Besides visual inspection of the forest plot, the I 2 statistic will be used to examine statistical heterogeneity of studies. Heterogeneity will be considered to be low at 0–40%, moderate at 30–60%, substantial at 50–90% and considerable at 75–100%.Reference Deeks, Higgins, Altman, Higgins, Thomas, Chandler, Cumpston, Li and Page33 We will interpret effect sizes following Cohen's suggestion (1992), in which a value of 0.2 indicates a small effect, 0.5 a medium effect and 0.8 a large effect. Statistical significance will be judged on P < 0.05.

Only studies with inactive control groups (i.e. no treatment, waiting list, TAU, placebo) that report outcomes on safety (frequency/intensity of IPV, danger assessment, safety-related behaviours), mental health (depression, PTSD, anxiety, psychological distress, suicidality or substance use) and/or psychosocial outcomes (perceived self-efficacy, personal resources, social support, decisional conflict, empowerment, quality of life) will be included in the meta-analysis. Further, only studies providing sufficient values (e.g. means, s.d., s.e.) to compute effect sizes for total scores will be eligible for analysis, since estimates rely on published data only. If a study reports multiple scales for the same outcome, the values for the measure most frequently applied will be included to keep heterogeneity as low as possible. If available, intention-to-treat data (ITT) will be used. We will perform a meta-analysis if at least three of the included studies report data on the same outcome.

We will use Review Manager version 5.4 (RevMan 5.4)36 to conduct the analyses.

Subgroup analysis

We will investigate predefined intervention and study characteristics as potential effect moderators. We will compare types of theoretical basis (presumably, advocacy versus psychological versus integrative interventions), types of intervention delivery mode (face-to-face versus digital interventions), types of intervention format (individual versus group), different treatment intensities (low-intensity interventions with 1–3 sessions versus medium-intensity interventions with 4–9 sessions or ≥6 months access to websites/apps versus high-intensity interventions with ≥10 sessions), treatment settings (shelter versus community versus clinical setting), resources of treatment settings (low- and middle-income countries versus low-resource settings in high-income countries versus high-income countries) and characteristics of inactive control conditions (TAU versus waiting list). Subgroup analysis will be feasible if three or more studies per subgroup are available.

Sensitivity analysis

We will conduct sensitivity analysis by excluding trials at high risk of bias and by excluding outliers.Reference Deeks, Higgins, Altman, Higgins, Thomas, Chandler, Cumpston, Li and Page33

Discussion

Effective and safe psychosocial interventions for survivors of IPV are required to prevent recurrence of violence and reduce negative health and psychosocial sequelae. With this systematic review and meta-analysis, we will provide a comprehensive overview of the current evidence base on various psychosocial interventions for IPV survivors. By integration of diverse populations, settings, interventions and outcomes, as well as inclusion of recently published studies, we will address limitations of previous systematic reviews and meta-analyses. We will quantitatively analyse the efficacy of psychosocial interventions for IPV survivors in improving safety and reducing related health and psychosocial impairment. Further, by performing subgroup analyses, we will investigate intervention and study characteristics that moderate the effectiveness of psychosocial interventions for survivors of IPV. Doing so, we aim to identify effective intervention approaches and promising lines of research. However, aside from these strengths, there are potential limitations that might affect the findings of this review. First, studies in the outlined research area are known to be of poor quality,Reference Rivas, Vigurs, Cameron and Yeo22,Reference Trabold, McMahon, Alsobrooks, Whitney and Mittal23,Reference Linde, Bakiewicz, Normann, Hansen, Lundh and Rasch37 which is likely to distort our effect estimates.Reference Savović, Turner, Mawdsley, Jones, Beynon and Higgins38 To detect bias potentially arising from methodological quality, we will perform sensitivity analyses, where only high-quality studies will be included. Second, because of the broad scope of this review, we expect substantial heterogeneity across studies, which reduces the confidence in our quantitative findings. We will address heterogeneity with subgroup analysis and reasonable selection of studies included in the meta-analyses.

Supplementary material

Supplementary material is available online at https://doi.org/10.1192/bjo.2022.625.

Data availability

Data availability is not applicable to this article as no new data were created or analysed in its preparation.

Author contributions

H.M.M., J.B. and L.B.S. conceptualised the study design. H.M.M., C.M.G. and L.B.S. developed and performed the search strategy. L.B.S and J.B. provided methodological expertise. C.M.G. and H.M.M. drafted the manuscript. L.B.S. and J.B. revised the manuscript. All authors read, gave feedback on and approved the final manuscript. All authors are accountable for every aspect of the work.

Funding

We acknowledge support by the Open Access Publication Fund of the University of Freiburg. Further, H.M.M. is supported by the Rosa Luxemburg Foundation (RLS). Other than that, this research received no specific grant from any funding agency, commercial or not-for-profit sectors.

Declaration of interest

None.

Appendix

Eligibility criteria

Participants

Individuals or couples with prior or current experience of IPV

Exclusion criteria: perpetrators (only)

Intervention

  1. (a) Interventions that explicitly target IPV, mental health and/or psychosocial outcomes

  2. (b) No restrictions on delivery mode (individual, couple, group, telephone, digital with or without guidance)

  3. (c) No restrictions on setting (e.g. healthcare, community, shelter or refuge)

  4. (d) No restriction on duration/intensity

Exclusion criteria:

  1. (a) Interventions for primary prevention of IPV (e.g. interventions targeting stigma, screening only)

  2. (b) Interventions designed for perpetrators only

  3. (c) Interventions designed for gatekeepers (e.g. family doctors, teachers)

  4. (d) Interventions targeting economic well-being only (e.g. cash transfer)

  5. (e) Interventions targeting associated symptoms only (e.g. safe sex)

  6. (f) Interventions providing physical safety or medical treatment only (e.g. shelter, refuge, crisis centre)

Comparator

  1. (a) Treatment as usual (TAU) (e.g. standard service care, informational session, unstructured counselling, routine prenatal, shelter or HIV care, informational websites)

  2. (b) Another treatment

  3. (c) Placebo (e.g. attention control, educational interventions on related topics)

  4. (d) Waiting list

  5. (e) No treatment

Outcomes

Any quantitative measure related to:

  1. (a) IPV (e.g. occurrence and frequency of IPV, safety-related behaviours)

  2. (b) Mental health (e.g. symptoms of depression, anxiety, PTSD, substance misuse, suicidal ideation, general mental health)

  3. (c) Psychosocial outcomes (e.g. quality of life, social functioning, self-esteem, self-efficacy, decisional conflict, social support, general distress)

Study design

  1. (a) Randomised controlled trials

  2. (b) Study protocols

References

World Health Organization. Violence against Women Prevalence Estimates, 2018: Global, Regional and National Prevalence Estimates for Intimate Partner Violence against Women and Global and Regional Prevalence Estimates for Non-Partner Sexual Violence against Women. WHO, 2021.Google Scholar
Laskey, P, Bates, EA, Taylor, JC. A systematic literature review of intimate partner violence victimisation: an inclusive review across gender and sexuality. Aggress Violent Behav 2019; 47: 1–11.CrossRefGoogle Scholar
Daoud, N, Matheson, FI, Pedersen, C, Hamilton-Wright, S, Minh, A, Zhang, J, et al. Pathways and trajectories linking housing instability and poor health among low-income women experiencing intimate partner violence (IPV): toward a conceptual framework. Women Health 2016; 56: 208–25.CrossRefGoogle ScholarPubMed
Showalter, K, Yoon, S, Logan, T. The employment trajectories of survivors of intimate partner violence. Work Employ Soc 2021; 2021: 095001702110352.CrossRefGoogle Scholar
Wathen, CN, MacGregor, JCD, MacQuarrie, BJ. Relationships among intimate partner violence, work, and health. J Interperson Violence 2018; 33: 2268–90.CrossRefGoogle ScholarPubMed
Bonomi, AE, Thompson, RS, Anderson, M, Reid, RJ, Carrell, D, Dimer, JA, et al. Intimate partner violence and women's physical, mental, and social functioning. Am J Prev Med 2006; 30: 458–66.CrossRefGoogle ScholarPubMed
Bacchus, LJ, Ranganathan, M, Watts, C, Devries, K. Recent intimate partner violence against women and health: a systematic review and meta-analysis of cohort studies. BMJ Open 2018; 8(7): e019995.CrossRefGoogle Scholar
Zara, G, Gino, S. Intimate partner violence and its escalation into femicide. Frailty thy name is “violence against women”. Front Psychol 2018; 9: 1777.CrossRefGoogle ScholarPubMed
Sprague, C, Woollett, N, Black, V, Hatcher, AM. How nurses in Johannesburg address intimate partner violence in female patients: understanding IPV responses in low- and middle-income country health systems. J Interperso Violence 2017; 32: 1591–619.CrossRefGoogle ScholarPubMed
Niolon, PH, Kearns, M, Dills, J, Rambo, K, Irving, S, Armstead, T, et al. Preventing Intimate Partner Violence Across the Lifespan: A Technical Package of Programs, Policies, and Practices. National Center for Injury Prevention and Control, Centers for Disease Control and Prevention, 2017 (https://www.cdc.gov/violenceprevention/pdf/ipv-technicalpackages.pdf).Google Scholar
Condino, V, Tanzilli, A, Speranza, AM, Lingiardi, V. Therapeutic interventions in intimate partner violence: an overview. Res Psychother Psychopath Process Outcome 2016; 19: 79–88.Google Scholar
García-Moreno, C, Hegarty, K, D'Oliveira, AFL, Koziol-McLain, J, Colombini, M, Feder, G. The health-systems response to violence against women. Lancet 2015; 385: 1567–79.CrossRefGoogle ScholarPubMed
Eckhardt, CI, Murphy, CM, Whitaker, DJ, Sprunger, J, Dykstra, R, Woodard, K. The effectiveness of intervention programs for perpetrators and victims of intimate partner violence. Partner Abuse 2013; 4: 196–231.CrossRefGoogle Scholar
Bair-Merritt, MH, Lewis-O'Connor, A, Goel, S, Amato, P, Ismailji, T, Jelley, M, et al. Primary care-based interventions for intimate partner violence: a systematic review. Am J Prev Med 2014; 46: 188–94.CrossRefGoogle ScholarPubMed
Karakurt, G, Whiting, K, van Esch, C, Bolen, SD, Calabrese, JR. Couples therapy for intimate partner violence: a systematic review and meta-analysis. J Marital Fam Ther 2016; 42: 567–83.CrossRefGoogle ScholarPubMed
Arroyo, K, Lundahl, B, Butters, R, Vanderloo, M, Wood, DS. Short-term interventions for survivors of intimate partner violence: a systematic review and meta-analysis. Trauma Violence Abuse 2017; 18: 155–71.CrossRefGoogle ScholarPubMed
Tirado-Muñoz, J, Gilchrist, G, Farré, M, Hegarty, K, Torrens, M. The efficacy of cognitive behavioural therapy and advocacy interventions for women who have experienced intimate partner violence: a systematic review and meta-analysis. Ann Med 2014; 46: 567–86.CrossRefGoogle ScholarPubMed
Anderson, EJ, McClelland, J, Krause, CM, Krause, KC, Garcia, DO, Koss, MP. Web-based and mHealth interventions for intimate partner violence prevention: a systematic review protocol. BMJ Open 2019; 9(8): e029880.CrossRefGoogle ScholarPubMed
Ogbe, E, Harmon, S, Van den Bergh, R, Degomme, O. A systematic review of intimate partner violence interventions focused on improving social support and/ mental health outcomes of survivors. PLoS One 2020; 15(6): e0235177.CrossRefGoogle ScholarPubMed
El Morr, C, Layal, M. Effectiveness of ICT-based intimate partner violence interventions: a systematic review. BMC Public Health 2020; 20(1): 1372.CrossRefGoogle ScholarPubMed
Linde, DS, Bakiewicz, A, Normann, AK, Hansen, NB, Lundh, A, Rasch, V. Intimate partner violence and electronic health interventions: systematic review and meta-analysis of randomized trials. J Med Internet Res 2020; 22(12): e22361.CrossRefGoogle ScholarPubMed
Rivas, C, Vigurs, C, Cameron, J, Yeo, L. A realist review of which advocacy interventions work for which abused women under what circumstances. Cochrane Database Syst Rev 2019; 6(6): CD013135.Google ScholarPubMed
Trabold, N, McMahon, J, Alsobrooks, S, Whitney, S, Mittal, M. A systematic review of intimate partner violence interventions: state of the field and implications for practitioners. Trauma Violence Abuse 2020; 21: 311–25.CrossRefGoogle ScholarPubMed
Howell, KH, Miller-Graff, LE, Hasselle, AJ, Scrafford, KE. The unique needs of pregnant, violence-exposed women: a systematic review of current interventions and directions for translational research. Aggress Violent Behav 2017; 34: 128–38.CrossRefGoogle Scholar
Cork, C, White, R, Noel, P, Bergin, N. Randomized controlled trials of interventions addressing intimate partner violence in sub-Saharan Africa: a systematic review. Trauma Violence Abuse 2020; 21: 643–59.CrossRefGoogle ScholarPubMed
Subirana-Malaret, M, Gahagan, J, Parker, R. Intersectionality and sex and gender-based analyses as promising approaches in addressing intimate partner violence treatment programs among LGBT couples: a scoping review. Cogent Soc Sci 2019; 5(1): 1644982.Google Scholar
Jonker, IE, Sijbrandij, M, van Luijtelaar, MJA, Cuijpers, P, Wolf, JRLM. The effectiveness of interventions during and after residence in women's shelters: a meta-analysis. Eur J Public Health 2015; 25: 15–9.CrossRefGoogle ScholarPubMed
Tarzia, L, Forsdike, K, Hegarty, K, Feder, G. Interventions in health settings for male perpetrators or victims of intimate partner violence. Trauma Violence Abuse 2020; 21: 123–37.CrossRefGoogle ScholarPubMed
Eisenhut, K, Sauerborn, E, García-Moreno, C, Wild, V. Mobile applications addressing violence against women: a systematic review. BMJ Global Health 2020; 5(4): e001954.CrossRefGoogle ScholarPubMed
Rivas, C, Ramsay, J, Eldridge, S, Sadowski, L, Davidson, LL, Dunne, D, et al. Advocacy interventions to reduce or eliminate violence and promote the physical and psychosocial well-being of women who experience intimate partner abuse. Cochrane Database Syst Rev 2015; 2015(12): CD005043.Google ScholarPubMed
Hameed, M, O'Doherty, L, Gilchrist, G, Tirado-Muñoz, J, Taft, A, Chondros, P, et al. Psychological therapies for women who experience intimate partner violence. Cochrane Database Syst Rev 2020; 7(7): CD013017.Google ScholarPubMed
Veritas Health Innovation. Covidence Systematic Review Software. Veritas Health Innovation, 2022. Available from: www.covidence.org.Google Scholar
Deeks, JJ, Higgins, JPT, Altman, DG. Analysing data and undertaking meta-analyses. In Cochrane Handbook for Systematic Reviews of Interventions, Version 6.3 (updated February 2022) (eds Higgins, J, Thomas, J, Chandler, J, Cumpston, M, Li, T, Page, M, et al. ). Cochrane, 2022: Ch. 10. Available from: www.training.cochrane.org/handbook.Google Scholar
Sterne, JAC, Sutton, AJ, Ioannidis, JPA, Terrin, N, Jones, DR, Lau, J, et al. Recommendations for examining and interpreting funnel plot asymmetry in meta-analyses of randomised controlled trials. BMJ 2011; 343: d4002.CrossRefGoogle ScholarPubMed
Ryan, R, Hill, S. How to GRADE the Quality of the Evidence. Cochrane Consumers and Communication Group, 2016.Google Scholar
Cochrane Collaboration. Review Manager (Version 5.4). Cochrane Collaboration, 2020.Google Scholar
Linde, DS, Bakiewicz, A, Normann, AK, Hansen, NB, Lundh, A, Rasch, V. Intimate partner violence and electronic health interventions: systematic review and meta-analysis of randomized trials. J Med Internet Res 2020; 22(12): e22361.CrossRefGoogle ScholarPubMed
Savović, J, Turner, RM, Mawdsley, D, Jones, HE, Beynon, R, Higgins, JPT, et al. Association between risk-of-bias assessments and results of randomized trials in Cochrane Reviews: the ROBES meta-epidemiologic study. Am J Epidemiol 2018; 187: 1113–22.CrossRefGoogle ScholarPubMed
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