Training healthcare providers to respond to intimate partner violence against women
Background Intimate partner violence (IPV) includes any violence (physical, sexual or psychological/emotional) by a current or former partner. This review reflects the current understanding of IPV as a profoundly gendered issue, perpetrated most often by men against women. IPV may result in substant...
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Veröffentlicht in: | Cochrane database of systematic reviews 2021-05, Vol.2021 (5), p.CD012423-CD012423 |
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Zusammenfassung: | Background
Intimate partner violence (IPV) includes any violence (physical, sexual or psychological/emotional) by a current or former partner. This review reflects the current understanding of IPV as a profoundly gendered issue, perpetrated most often by men against women. IPV may result in substantial physical and mental health impacts for survivors. Women affected by IPV are more likely to have contact with healthcare providers (HCPs) (e.g. nurses, doctors, midwives), even though women often do not disclose the violence. Training HCPs on IPV, including how to respond to survivors of IPV, is an important intervention to improve HCPs' knowledge, attitudes and practice, and subsequently the care and health outcomes for IPV survivors.
Objectives
To assess the effectiveness of training programmes that seek to improve HCPs' identification of and response to IPV against women, compared to no intervention, wait‐list, placebo or training as usual.
Search methods
We searched CENTRAL, MEDLINE, Embase and seven other databases up to June 2020. We also searched two clinical trials registries and relevant websites. In addition, we contacted primary authors of included studies to ask if they knew of any relevant studies not identified in the search. We evaluated the reference lists of all included studies and systematic reviews for inclusion. We applied no restrictions by search dates or language.
Selection criteria
All randomised and quasi‐randomised controlled trials comparing IPV training or educational programmes for HCPs compared with no training, wait‐list, training as usual, placebo, or a sub‐component of the intervention.
Data collection and analysis
We used standard methodological procedures outlined by Cochrane. Two review authors independently assessed studies for eligibility, undertook data extraction and assessed risks of bias. Where possible, we synthesised the effects of IPV training in a meta‐analysis. Other analyses were synthesised in a narrative manner. We assessed evidence certainty using the GRADE approach.
Main results
We included 19 trials involving 1662 participants. Three‐quarters of all studies were conducted in the USA, with single studies from Australia, Iran, Mexico, Turkey and the Netherlands. Twelve trials compared IPV training versus no training, and seven trials compared the effects of IPV training to training as usual or a sub‐component of the intervention in the comparison group, or both.
Study participants included 618 medical staff/ |
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ISSN: | 1465-1858 1465-1858 1469-493X |
DOI: | 10.1002/14651858.CD012423.pub2 |