Primary Objective: Our primary objective is to determine if it is acceptable to patients in the trauma clinic for orthopaedic/trauma surgeons, orthopaedic/trauma nurses, and/or social workers in the trauma clinic to screen for IPV.Secondary…
ID
Source
Brief title
Condition
- Other condition
- Bone and joint injuries
Synonym
Health condition
Elk type traumatisch letsel gepresenteerd op de SEH (vb. contusies, distorsies, fracturen, (brand)wonden)
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
Our primary questionnaire is a self-report written questionnaire developed by
the IVP study group of the McMaster University. Methodological and IPV experts
were consulted in the development of the questionnaire.
Our primary parameter is to assess the patient*s opinion of screening both men
and women for IPV in the fracture clinic, who should perform the screening, how
screening should occur, and who should be screened.
Secondary outcome
The questionnaire will also record the characteristics of the patients,
including age, income, education, race/ethnicity, marital status, sexual
orientation, and length of relationship. We will also record the type of
injury for which the patient is being treated.
Background summary
Intimate partner violence (IPV) is described by the American Medical
Association as *a pattern of coercive behaviors that may include repeated
battering and injury, psychological abuse, sexual assault, progressive social
isolation, deprivation, and intimidation*. The long-term consequences of IPV
include health risks, posttraumatic stress disorder, depression, and staggering
economic costs for health care of victims. Victims of IPV make more use of
healthcare than woman who are not involved in IPV.
A survey in 1992 showed that 21% of women in the Netherlands have experienced
physical or sexual violence in a marital or common-law union. In half of these
women it concerned severe physical violence in the current relationship. The
Journal of Trauma reports that the cumulative lifetime prevalence of domestic
violence for women admitted to the emergency department is 54%.
However, IPV is underreported among women who seek medical attention. The
American College of Surgeons position statement on IPV states that surgeons
have the responsibility to identify IPV and appropriately treat women at risk
of further harm (The American College of Surgeons, 2008). We are currently
conducting a study assessing prevalence of IPV in orthopedic and trauma clinics
(PRAISE, MEC 10/042). A pilot study of the PRAISE, conducted in Ontario,
suggests that the high prevalence of IPV in orthopedic trauma clinics warrants
additional resources to identify and manage victims. We seek to assess the
patients attitudes of screening for IPV in orthopedic fracture clinics to
establish if and how patients consider it acceptable to screen for IPV in
orthopedic and/or trauma clinics.
Study objective
Primary Objective:
Our primary objective is to determine if it is acceptable to patients in the
trauma clinic for orthopaedic/trauma surgeons, orthopaedic/trauma nurses,
and/or social workers in the trauma clinic to screen for IPV.
Secondary Objective(s):
- Whether screening male patients for IPV in the trauma clinic is acceptable to
patients?.
- Who patients in the trauma clinic prefer to screened by for IPV (surgeons,
nurses, social workers).
- How patients prefer screening to occur (what questions should be asked, where
and when should screening occur, how long
should health care providers spend on screening etc.).
- Whether men*s attitudes about screening for IPV differ from women*s.
Study design
A cross sectional multicentre study will be performed wherein 750 women and men
will complete a self-reported written questionnaire across three clinical sites
in Canada, in the Academic Medical Center and Onze Lieve Vrouwe Gasthuis in
Amsterdam.
Recruitment of 150 participants will take place at the trauma or orthopedic
clinic at each clinical site. The questionnaires will contain a set of
questions used to asses opinions towards screening for IPV, as well as
questions pertaining to the participant*s demographics.
The measurement instruments that we have selected to use is a self-report
written questionnaire developed by the McMaster University IPV study group and
will be translated in Dutch. Methodological and IPV experts were consulted in
the development of the questionnaire.
Study burden and risks
If screening for IPV in orthopedic and/or trauma clinics is acceptable to the
majority of patients, this study will serve to advocate for the continued
education of medical professionals to better recognize probable IPV cases and
offer existing services to enhance the care of these patients. This is
especially important because healthcare providers who receive education on
screening and ways to care for IPV victims detect them more readily7.
Furthermore, this study may encourage more open communication between
orthopedic and/or trauma surgeons and their patients, as two major barriers to
IPV detection are either the patient is never asked8 or the healthcare provider
is reluctant to inquire9-11.
Harm for the individual will be minimized by respecting the participant*s
privacy and affirming to him / her that the care she receives is in no way
affected by her decision to participate or not participate in the study. Due
to the nature of the research topic, care must be exercised when recruiting
individuals to participate in the study. Although this study does not ask
participants to disclose IPV, patients may be afraid of speaking about IPV for
fear of retaliation from the offender, stigmatization, embarrassment, and
police involvement7. Because of this fear, key ethical issues addressed in this
study are
1) requirement for free and informed consent,
2) respect for privacy and confidentiality, and
3) maximizing benefit.
To maximize benefit, individuals who are approached to participate in the study
will be offered information resources pertaining to IPV and contact information
of local IPV services in the clinic area. Trauma clinic staff will also be
aware of the study and will also be provided with these materials in the event
that the individual approached would prefer to speak to her care provider(s)
about IPV instead of members of the study team.
Meibergdreef 9
1105 AZ Amsterdam
NL
Meibergdreef 9
1105 AZ Amsterdam
NL
Listed location countries
Age
Inclusion criteria
1) The patient presents to the outpatient trauma/orthopedic clinic for his/her own appointment.
2) The patient is 18 years of age or older.
3) The patient is able to read, understand, and write in Dutch or English.
4) The patient is being seen at the trauma or orthopedic outpatient clinic for the treatment of a traumatic injury.
5) The patient is able to separate him/herself from anyone who accompanied her to the trauma clinic in order to complete the questionnaire in privacy.
Exclusion criteria
1) The patient is considered too ill or injured to participate in the study.
2) The patient is cognitively impaired and unable to participate in the study.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL34413.018.11 |