Knowledge, Attitudes, and Beliefs Outcome
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
Medical students (Ernst et al., 1998, 2000) |
Type: Didactic Length: 3 hrs. Clinical aids: None |
|
One group |
Knowledge re IPV |
Self-report (14 items) |
|
Medical students (Haase et al., 1999) |
Type: Mixed Length: 9 hrs. over 6 weeks Clinical aids: None |
None |
Two groups (one comparison group) |
Perceived comfort, preparedness, questioning habits, and knowledge of resources re IPV |
Self-report (five items, a = 0.70 |
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
Yes |
1 |
24 |
Eligible = 148 Pre = 144 Post = 141 (98%) FU = 104 (72%) |
|
Ipost>Ipre* (6 items) IFU >Ipre* (5 items) IFU <Ipost* (2 items) IFU =Ipost (8 items) |
|
Within-group comparisons were not based on matched groups (e.g., those with complete data and on all measurement waves) due to the Institutional Review Board’s requirement that participants be anonymous. Thus, the comparisons should be interpreted with caution. |
|
No |
24 |
|
Eligible = Not reported Post = 29 |
Eligible = Not reported Post = 86 |
|
Ipost>Cpost* |
Although the training was a formal elective course, groups were created by self-report on the posttest rather than known course enrollment. The analysis controlled for gender. Analyses of individual items indicated that group differences were in knowledge and reported questioning habits rather than comfort and preparedness. |
Knowledge, Attitudes, and Beliefs Outcome
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
Medical students (Jonassen et al., 1999) |
Type: Mixed Length: 2-3.5 days |
|
One group |
Knowledge re IPV |
Self-report (10 items) |
|
Clinical aids: Materials on local resources; screening algorithm |
Attitudes re IPV |
Self-report (26 items) |
|||
|
Clinical skills and experience |
Self-report (10 items) |
||||
|
Medical students (Short et al., 2000) |
Type: Mixed Length: 4-week module Clinical aids: None |
One lecture |
Two groups (one comparison group) |
Knowledge, attitudes, and behavioral intentions about IPV |
Self-report (37 items, a = 0.80, test-retest = 0.87) |
|
|
Appropriateness of intervening |
Self-report (3-item subscale, a = 0.51, test-retest = 0.64) |
|||
|
Physician responsibility for IPV |
Self-report (8-item subscale, a = 0.69, test-retest = 0.82) |
||||
|
Victim autonomy for decisions |
Self-report (3-item subscale, a = 0.54, test-retest = 0.69) |
||||
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
Yes |
Immediately after training |
6 |
Eligible = 205 Pre, Post, and FU = 144 (70%) |
|
Ipost >Ipre* IFU >Ipre* |
|
Test reliability was reported as adequate. |
|
Ipost >Ipre* IFU >Ipre* Ipost >Ipre* IFU >Ipre* |
Results pertain to comparisons for two separate cohorts. |
||||||
|
Yes |
1 |
|
Eligible = 149 Pre = 124 Post = 87 (70%) |
Eligible = 97 Pre = 88 Post = 66 (75%) |
Ipost >Ipre* |
Ipost >Cpost* |
|
|
Ipost < Ipre |
Ipost <Cpost |
||||||
|
Ipost >Ipre |
Ipost >Cpost |
||||||
|
Ipost >Ipre |
Ipost >Cpost |
||||||
Knowledge, Attitudes, and Beliefs Outcome
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
|
Self-efficacy for detecting IPV |
Self-report (6-item subscale, a = 0.72, test-retest = 0.72) |
|||
|
Behavioral intentions to screen |
Self-report (6-item subscale, a = 0.66, test-retest = 0.83) |
||||
|
Residents in all specialties (Coonrod et al., 2000) |
Type: Mixed Length: 20 min. Clinical aids: Articles and pocket information cards |
Didactic educational session on unrelated topic Length: 20 min. Clinical aids: Articles and pocket information cards on topic |
Two groups (randomized) |
Knowledge of IPV |
Self-report (5-item subscale) |
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
|
Ipost >Ipre* |
Ipost >Cpost* |
|
||||
|
Ipost >Ipre* |
Ipost >Cpost* |
|
|||||
|
Yes |
9-10 |
|
Eligible = 24 Pre = 24 Post = 12 (50%) |
Eligible = 22 Pre = 22 Post = 11 (50%) |
|
Ipost >Cpost* |
Analysis controlled for pretest score. Results |
Knowledge, Attitudes, and Beliefs Outcome
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
Residents in internal medicine (Knight et al., 2000) |
Type: Didactic Length: 105 min. Clinical aids: Local resource list; laminated card of screening questions and resource contacts |
|
One group |
Beliefs re IPV (including selfefficacy of victims) |
Self-report (31 items) |
|
Residents in internal medicine (Kripke et al., 1998) |
Type: Mixed Length: 4 hrs. Clinical aids: None |
One group |
Knowledge re IPV |
Self-report (10 items) |
|
|
Attitudes re IPV |
Self-report (25 items) |
||||
|
Perceptions re skills |
Self-report (10 items) |
||||
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
Yes |
Immediately after training |
|
Eligible = 45 Pre = 45 Post = 45 (100%) |
|
Ipost =Ipre |
|
Measures used were those developed by Varvaro et al. (1997), who reported internal consistencies ranging from 0.62 to 0.90, depending on the subscale of interest. Results were affected by residents = complaints about the lengthiness of the survey and their careless responding. |
|
Yes |
Immediately after training |
6 |
Eligible = 55 Pre = 55 Post = 55 (100%) FU = 55 (100%) |
Ipost >Ipre* IFU >Ipre* Ipost >Ipre* IFU >Ipre* Ipost >Ipre* IFU =Ipre |
The differences would have been statistically significant if a one-tailed test had been used. |
||
Knowledge, Attitudes, and Beliefs Outcome
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
ED staff and emergency medical technicians (Allert et al., 1997) |
Type: Didactic Length: 90 min. Clinical aids: Copy of care guidelines; list of local resources |
|
One group |
Knowledge of written protocol, reporting requirements, and documentation |
Self-report (4 items) |
|
ED nurses (Bokunewicz & Copel, 1992) |
Type: Didactic Length: 60 min. Clinical aids: None |
One group |
Beliefs re IPV |
Self-report (questions on a scenario, a = 0.79) |
|
|
ED staff, including physicians, nurses, and social workers (Campbell et al., in press) |
Type: Mixed Length: 2 days Clinical aids: Technical assistance if requested |
Usual or available training |
Two groups (group randomized) |
Knowledge and attitudes about IPV |
Self-report (23 items, a = 0.73) |
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
Yes |
Immediately after training |
3 |
Eligible = 329 Pre = 266 Post = 266 (100%) FU = 213 (80%) |
|
Ipost >Ipre* (6 items) IFU >Ipre* (6 items) |
|
Total number of items in the instrument was not specified. The follow-up was done by telephone to a random sample, but the response rate was not reported. It is unclear whether the statistical tests took into account repeated measures. |
|
Yes |
Immediately after training |
|
Eligible = 42 Pre = 18 Post = 18 (100%) |
Ipost >Ipre* |
|
||
|
Yes |
18-24 |
|
3 EDs Eligible = Not reported Pre = Not reported Post = 330 |
3 EDs Eligible = Not reported Pre = Not reported Post = 319 |
Ipost >Ipre* |
Ipost >Cpost* |
An overall response rate for the posttest was 75%, but no information was provided regarding differential response rates for the two groups. The analyses controlled for gender, state, and pretest standing. |
Knowledge, Attitudes, and Beliefs Outcome
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
Trauma center staff, including residents in surgery and emergency medicine, medical students, and surgeons (Davis et al., 2000) |
Type: Didactic Length: Unclear Clinical aids: None |
|
One group |
Knowledge re IPV |
Self-report (18 items) |
|
ED staff, including physicians, interns, and nurses (Roberts et al., 1997b) |
Type: Didactic Length: 1 hr. Clinical aids: Poster (protocol); pocket cards |
One group |
Knowledge of IPV |
Self-report (43 items) |
|
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
Yes |
Immediately after training |
|
Eligible = Not reported Pre = 92 Post = 92 (100%) |
Ipost >Ipre* |
|
||
|
Yes |
Immediately after training |
Physicians Eligible = 72 Pre = 31 Post = 20 (65%) Nurses Eligible = 91 Pre = 69 Post = 48 (70%) |
|
Ipost >Ipre* |
|
There were significant changes for the combined group of physicians and nurses, but nurses increased more than physicians. Overall, physicians incrased significantly but only in terms of knowledge of legal aspects of IPV. |
|
Knowledge, Attitudes, and Beliefs Outcome
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
|
Attitudes toward IPV |
Self-report (10 items) |
|||
|
ED, critical care, and perinatal hospital staff (Short et al., in press) |
Type: Length: Clinical aids: Protocol |
Usual and available |
Two groups (one comparison group) |
Knowledge, attitudes, and behavioral intentions about IPV |
Self-report (51 items) |
|
|
Understanding of abusive relationships |
Self-report |
|||
|
Beliefs about staff preparation and ability for addressing IPV |
|
||||
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
|
Ipost >Ipre |
|
After training, 35% of physicians believed that there was little a doctor or nurse could do to stop IPV, 50% believed that victims did not want to discuss IPV with a health professional, and 45% did not know that emotional abuse is generally viewed as worse than physical abuse by victims. |
||||
|
Yes |
12 |
12 |
Eligible = 417 Pre = 200 Post = |
Eligible = 265 Pre = 127 Post = |
IFU2 >Ipre |
IFU2 >CFU2* |
Although exact results were not provided, the authors reported that psychometric analyses found the scales were internally consistent. A total of 211 individuals had complete data for the outcome |
|
|
IFU2 >Ipre |
IFU2 <CFU2 |
|||||
|
IFU2 >Ipre |
IFU2 >CFU2* |
||||||
Knowledge, Attitudes, and Beliefs Outcome
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
ED, critical care, and perinatal hospital staff |
|
Victim autonomy for decisions |
Self-report |
||
|
Staff responsibility to address domestic violence |
Self-report |
||||
|
Self-efficacy for detecting IPV and interacting with victims |
Self-report |
||||
|
Self-efficacy for referral and services |
Self-report |
||||
|
Own behaviors re screening and documentation |
Self-report |
||||
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
|
IFU2 >Ipre |
IFU2 > CFU2* |
analyses, yielding an overall response rate for the posttest of 65%. The extent to which differential attrition occurred between groups was not reported. Analyses controlled for age, gender, position, department, exposure to training, and pretest score. |
||||
|
IFU2 >Ipre |
IFU2 >CFU2 |
||||||
|
IFU2 >Ipre* |
IFU2 >CFU2 |
||||||
|
IFU2 >Ipre* |
IFU2 >CFU2 |
||||||
|
IFU2 >Ipre* |
IFU2 >CFU2* |
||||||
Knowledge, Attitudes, and Beliefs Outcome
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
ED house staff (Varvaro et al., 1997) |
Group 1 Type: Didactic Length: 1 hr. Clinical aids: None Group 2 Type: Didactic Length: 1 hr. Clinical aids: pocket IPV training manual |
Usual and available |
Two groups (one comparison group) |
Beliefs about IPV |
Self-report (12 items, a = 0.89) |
|
Attitudes re IPV (self-efficacy in IPV victims) |
Self-report (31 items, as ranged from 0.62 to 0.90 for subscales) |
||||
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
Yes |
0.5 |
|
Group 1 Eligible = Not reported Pre = 13 Post = 13 (100%) |
Eligible = Not reported Pre = 11 Post = 11 (100%) |
Ipost =Ipre |
Ipost =Cpost |
The lecture-only and the lecture plus manual groups differed on specific items regarding perceived self-efficacy at the posttest, but the differences did not consistently favor one group. No comparisons were made between these two groups and the control group. The ability to detect within-group changes and relative group differences was handicapped by the small sample sizes. |
|
Group 2 Eligible = Not reported Pre = 13 Post = 13 (100%) |
Ipost >Ipres (5 of 12 items) |
||||||
Knowledge, Attitudes, and Beliefs Outcome
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
Community health center staff, including physicians, midlevel practitioners, social workers, and psychologists (Harwell et al., 1998) |
Type: Mixed Length: 3-6 hrs. Clinical aids: IPV screening pocket card; IPV assessment form; stamp to indicate screening and suspected or confirmed abuse; patient card of resources and safety tips; additional tailored follow-up training to some CHCs |
|
One group |
Knowledge of IPV |
Self-report (13 items, a = 0.91) |
|
Attitudes (comfort with IPV) |
Self-report (4 items, a = 0.82) |
||||
|
Nurse-midwives (Paluzzi et al., 2000) |
Type: Unclear Length: 8 hrs. Clinical aids: None |
|
One group |
Knowledge re IPV |
Self-report (a = 0.80) |
|
Attitudes re IPV |
Self-report (a = 0.61) |
||||
|
Level of comfort in working with victims |
Self-report (a = 0.59) |
||||
|
Perceived cultural competence |
Self-report (a = 0.96) |
||||
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
Yes |
Immediately after training |
3 |
Eligible = 108 Pre = 108 Post = 108 (100%) FU = 23 of 66 eligible (35%) |
|
Ipost >Ipre* IFU >Ipre* IFU <Ipre |
|
Analyses were restricted to the direct care providers who received the training. Table 2 is not clear as to whether results at all waves were only for 23 in the follow-up. |
|
Ipost >Ipre* IFU >Ipre IFU <Ipost |
|||||||
|
Yes |
6 |
12 |
Eligible = Not reported Pre = 165 Post = 80 (48%) FU = 23 (14%) |
|
Ipost >Ipre* IFU >Ipost |
|
|
|
Ipost >Ipre* IFU >Ipost |
|||||||
|
Ipost >Ipre* IFU >Ipost |
|||||||
|
Ipost >Ipre* IFU >Ipost |
|||||||
Knowledge, Attitudes, and Beliefs Outcome
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
Primary care team members (Thompson et al., 2000) |
Type: Mixed Length: two half-day sessions over 12 months Clinical aids: Posters; provider cue cards; routine exam forms; feedback |
Usual and available training (e.g., manual) |
Two groups (group randomized) |
Self-efficacy re detecting IPV |
Self-report (7-item subscale, a = 0.73) |
|
System support |
Self-report (4-item subscale, a = 0.73) |
||||
|
Blaming the victim |
Self-report (7-item subscale, a = 0.80) |
||||
|
Fear of offending |
Self-report (7-item subscale, a = 0.80) |
||||
|
Safety concerns |
Self-report (8-item subscale, a = 0.91) |
||||
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
Yes |
9 |
21 |
Two clinics Eligible = Not reported Pre = 91 Post = Not reported FU =Not reported |
Three clinics Eligible = Not reported Pre =88 Post =Not reported FU =Not reported |
Ipost >Ipre* IFU >Ipre* |
Ipost >Cpost* IFU >CFU* |
Total number of eligible participants in all clinics was 208 of which 179 (86%) responded to the pretest.At the posttest and follow-up,there were 190 eligible providers of which 79% responded,and the corresponding figures for the follow-up were 171 and 82%.The extent to which the two groups differed with regard to attrition was not reported. Outcome analyses were adjusted for pretest and clustering. |
|
Ipost >Ipre IFU =Ipre |
Ipost >Cpost IFU >CFU |
||||||
|
Ipost >Ipre IFU =Ipre |
Ipost >Cpost IFU >CFU |
||||||
|
Ipost >Ipre* IFU >Ipre* |
Ipost >Cpost IFU >CFU* |
||||||
|
Ipost >Ipre* IFU >Ipre* |
Ipost >Cpost IFU >CFU* |
||||||
Outcomes Related to Clinical Intervention Practices
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
Residents in internal medicine and family practice (Saunders et al.,1993) |
Type: Mixed Length: Two 50-min. sessions or one 2-hr. session Clinical aids: None Number of participants: 17 |
Usual and available |
Two groups, randomized |
% covering psychosocial issues in patient interview |
Standardized patient visit |
|
Extent to which history was taken during patient interview |
Standardized patient visit |
||||
|
Extent of planning conducted during patient interview |
Standardized patient visit |
||||
|
ED staff, including physicians, nurses, and social workers (Campbell et al., in press) |
Type: Mixed Length: 2 days Clinical aids: Technical assistance if requested |
Usual or available training |
Two groups (group randomized) |
% of identified IPV cases with more appropriate interventions |
Chart review |
|
Patient satisfaction with care received |
Self-report of patients |
||||
|
Commitment by EDs to detecting and treating IPV victims |
Researcher ratings |
||||
|
ED staff (Fanslow et al. 1998, 1999) |
Type: Didactic Length: 1 or 4 hrs. Clinical aids: Protocols; forms; body map; checklist; contact cards Number of participants: 33 nurses and 11 medical staff |
|
Cohort |
% of IPV cases where interventions were used (e.g., referrals) |
Chart review |
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
No |
6 |
|
Post = 15 |
Post = 20 |
|
Ipost =Cpost |
|
|
Unclear |
|||||||
|
Unclear |
|||||||
|
Yes |
12 |
18 |
3 hospitals: Pre = 600 Post = 600 FU = 600 |
3 hospitals: Pre = 600 Post = 600 FU = 600 |
Ipost =Cpost |
||
|
Ipost >Cpost* |
|||||||
|
Ipost >Ipre* IFUt>Ipre* |
Ipost >Cpost* IFUt>CFUt* |
||||||
|
Yes |
12 |
|
Pre = 21 Post = 34 |
Pre = 26 Post = 13 |
Ipost >Ipre* |
Ipost >Cpost* IFU =CFU |
There was a difference in the number of interventions at the baseline. |
Outcomes Related to Clinical Intervention Practices
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
Community health center staff, including physicians, midlevel practitioners, social workers, and psychologists (Harwell et al., 1998) |
Type: Mixed Length: 3-6 hrs. Clinical aids: IPV screening pocket card; IPV assessment form; stamp to indicate screening and suspected or confirmed abuse; patient card of resources and safety tips; additional tailored followup training to some CHCs Number of participants: 108 |
|
Cohort |
% of all cases with a completed safety assessment |
Chart review |
|
% of all cases where a body map was completed |
Chart review |
||||
|
% of all cases with referral to CHC staff |
Chart review |
||||
|
% of all cases with referrals to outside agencies |
Chart review |
||||
|
Public health nurses (Shepard et al., 1999) |
Type: Mixed Length: 4 hrs. Clinical aids: Protocol and follow-ups Number of participants: Unclear |
Cohort |
% of identified IPV cases who were provided information |
Chart review |
|
|
% of identified IPV cases who were directly referred to |
Chart review services |
||||
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
Yes |
6 |
|
Pre = 251 Post = 255 |
|
Ipost >Ipre* |
|
|
|
Ipost =Ipre |
|||||||
|
Ipost >Ipre |
|||||||
|
Ipost >Ipre* |
|||||||
|
Yes |
12 |
24 |
Pre = 31 Post = 23 FU = 18 |
Ipost >Ipre* IFU >Ipre* |
|
Analyses controlled for age of patients. |
|
|
Ipost >Ipre IFU >Ipre |
|||||||
Outcomes Related to Clinical Intervention Practices
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
ED, critical care, and perinatal hospital staff (Short et al., in press) |
Type: Length: Clinical aids: Protocol |
Usual and available |
Two groups (one comparison group) |
% of cases with documentation of relevant social history |
Chart review |
|
% of cases with documentation |
Chart review |
||||
|
% of documented referrals for IPV cases |
Chart review |
||||
|
Primary care team members (Thompson et al., 2000) |
Type: Mixed Length: 2 halfday sessions over 12 months Clinical aids: Posters; provider cue cards;routine exam firms; feedback Number of participants: Unclear |
Usual and available training (e.g., manual) |
Two groups (group randomized) |
% of identified IPV cases whose quality of care was judged good or excellent |
Chart review |
|
Prenatal health clinic staff, including physicians, nurses, nutritionists, counselors, and clerical staff (Wist & McFarlane, 1999) |
Type: Didactic Length: 90 min. Clinical aids: Protocol; follow-up Number of participants: Unclear |
No protocol in one clinic |
Two groups (one comparison group) |
% of identified IPV cases who received referrals to outside agencies |
Chart review |
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
|
15 |
18 21 24 |
Post, FU1, FU2, FU3 = Not reported |
Post, FU1, FU2, FU3 = Not reported |
|
IFU3 > CFU3* |
A total of 2,531 charts were reviewed, but the numbers were not reported for each data collection wave. |
|
IFU3>CFU3 |
|||||||
|
IFU3>CFU3* |
|||||||
|
Yes |
9-10 |
|
2 clinics Pre = 27 Post = 37 |
3 clinics Pre = 32 Post = 35 |
Ipost =Ipre Cpost =Cpre |
Ipost =Cpost |
|
|
Yes |
3 |
12 |
Pre = 3 Post = 9 FU = 17 |
Pre = 0 Post = 0 FU = 0 |
IFU >Ipre* |
|
|
Screening, Identification, and Detection of Intimate Partner Violence
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
Medical students (Jonassen et al., 1999) |
Type: Mixed Length: 2-3.5 days Clinical aids: Materials on local resources; screening algorithm |
Earlier cohort of third-year medical students who did not participate in the clerkship |
Three groups (one comparison group) |
Screening skills |
Standardized patient |
|
Medical students (Short et al., 2000) |
Type: Mixed Length: 4-week module Clinical aids: None |
One lecture |
Two groups (one comparison group) |
% correctly identifying IPV in patient |
Vignettes |
|
% correctly identifying IPV in patient |
Standardized patient |
||||
|
Residents in family practice (Bolin & Elliott, 1996) |
Type: Didactic Length: 2 hrs. Clinical aids: List of contacts; button |
Type: Didactic Length: 2 hrs. Clinical aids: List of contacts |
Two groups, randomized |
No. of days that resident had conversations with patients about IPV |
Self-report of residents (daily diary) |
|
Residents in internal medicine (Knight et al., 2000) |
Type: Didactic Length: 105 mins. Clinical aids: Local resource list; laminated card of screening questions and resource contacts Number of participants: 45 |
|
1 group |
% of patients reporting that resident had asked about IPV |
Patient exit interview (one item) |
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
|
9 |
|
Eligible = 205 Post = 205 (100%) |
Eligible = 93 Post = 93 (100%) |
|
Ipost >Cpre* |
Test reliability was reported as adequate. Results pertain to two separate cohorts who received the training. |
|
Yes |
1 |
Eligible = 149 Pre = 124 Post = 88 (71%) |
Eligible (97) Pre = 88 Post = 66 (75%) |
Ipost <Ipre* |
Ipost =Cpost |
The standardized patient was designed as test of interview techniques. |
|
|
No |
1 |
|
Ipost =Cpost |
||||
|
No |
1 |
|
Eligible = Not reported Post = 6 |
Eligible = Not reported Post = 5 |
|
Ipost >Cpost* |
|
|
Yes |
4 days |
Pre = 122 Post = 116 |
|
Ipost >Ipre* |
|
Analyses were adjusted for patient age, income, and education, along with physician race. |
|
Screening, Identification, and Detection of Intimate Partner Violence
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
Residents in internal medicine (Kripke et al., 1998) |
Type: Mixed Length: 4 hrs. Clinical aids: None Number of participants: 55 |
|
One group |
% of cases seen where patient was asked about IPV |
Chart review |
|
% of cases where patient was identified as IPV victim |
Chart review |
||||
|
Residents in family practice (Mandel & Marcotte, 1983) |
Type: Mixed Length: Two sessions over 4 months Clinical aids: Checklist on appropriate practices Number of participants: 16 |
Usual and available |
Two groups (one comparison group) |
% identifying IPV |
Standardized patient visit |
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
Yes |
6 |
|
Pre = 693 Post = 277 |
|
Ipost >Ipre |
|
|
|
Ipost <Ipre |
|||||||
|
|
4 |
|
Eligible = Not reported Post = 10 |
Eligible = Not reported Post = 6 |
|
Ipost =Cpost |
Due to the small sample sizes, no statistical tests were performed. |
Screening, Identification, and Detection of Intimate Partner Violence
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
Residents in internal medicine and family practice (Saunders et al., 1993) |
Type: Mixed Length: Two 50-min. sessions or one 2-hr. session Clinical aids: None Number of participants: 17 |
Usual and available |
Two groups, randomized |
Time needed to detect IPV in interview |
Standardized patient visit |
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
No |
6 |
|
Eligible = Not reported Post = 15 |
Eligible = Not reported Post = 20 |
|
Ipost =Cpost |
Randomization was done by team in one site, and those who did not attend training were placed randomly in rotation sites. The outcome was in the expected direction but was not significant after physician gender, prior professional exposure, and number of IPV victims known were controlled for. |
Screening, Identification, and Detection of Intimate Partner Violence
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
ED staff, including physicians, nurses, and social workers (Campbell et al., in press) |
Type: Mixed Length: 2 days Clinical aids: Technical assistance if requested |
Usual or available training |
Two groups (groups randomized) |
% of women who asked about IPV |
Self-report of patients |
|
% of self-identified IPV victims documented as such on medical record |
Chart review |
||||
|
ED psychiatric staff, including residents, medical students, and other staff (Currier & Briere, 2000) |
Type: Didactic Length: 1 hr. Clinical aids: Protocol Number of participants: 10 |
Protocol only (8 staff) |
Two groups, randomized |
% of patients seen by staff where history of adult spouse abuse was identified in chart |
Chart review |
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
Yes |
9-12 |
18-24 |
Pre = Not reported Post = 330 |
Pre = Not reported FU2 = 319 |
IFU >Ipre* |
Ipost <Cpost IFU >CFU |
Analyses controlled for baseline differences. Although not statistically significant due to low statistical power, the ratio of self-reported IPV cases by patients to those documented in the medical record increased in the experimental hospitals but decreased in the comparison hospitals. |
|
Ipost >Cpost IFU >CFU |
|||||||
|
No |
Unclear |
|
Post = 84 patients |
Post = 78 patients |
|
Ipost >Cpost* |
|
Screening, Identification, and Detection of Intimate Partner Violence
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
ED staff (Fanslow et al., 1998, 1999) |
Type: Didactic Length: 1 or 4 hrs. Clinical aids: Protocols; forms; body map; checklist; contact cards Number of participants: 33 nurses and 11 medical staff |
|
Cohort |
% of all cases identified as IPV victims |
Chart review |
|
% of possible IPV cases that were confirmed |
Chart review |
||||
|
% of possible IPV cases with documentation |
Chart review |
||||
|
ED staff (McLeer et al., 1989) |
Type: Unclear Length: Unclear Clinical aids: Protocol Number of participants: Not clear |
|
Cohort |
% of all cases identified as IPV |
Chart review |
|
ED physicians (Olson et al., 1996) |
Type: Didactic Length: 1 hr. Clinical aids: Stamped query on patient form Number of participants: Unclear |
|
Cohort |
% of all cases identified as IPV |
Chart review |
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
Yes |
1-3 |
12-15 |
Pre = 2276 Post = 2287 FU = 1598 |
Pre = 1768 Post = 1720 FU = 1312 |
Ipost =Ipre |
Ipost =Cpost IFU =CFU |
The analyses did not incorporate additional variables (e.g., patient characteristics). |
|
Pre = 57 Post = 53 FU = 17 |
Pre = 54 Post = 45 FU = 30 |
Ipost >Ipre* |
Ipost > Cpost* IFU =CFU |
||||
|
Pre = 57 Post = 53 FU = 17 |
Pre = 54 Post = 45 FU = 17 |
Ipost >Ipre*I |
post >Cpost* IFU =CFU |
Routine screening not adopted by ED staff. |
|||
|
Yes |
12 |
96 |
Pre = 359 Post = 412 FU2 = 470 |
|
Ipost >Ipre* IFU >Ipre IFU < Ipost* |
|
At follow-up, the protocol was no longer in use nor any other formal assessment procedure. |
|
|
1 mo. prior |
1 |
Pre = 1,272 Stamp-only = 1,444 Stamp & training = 1,356 |
|
Ipost >Ipre* IFU >Ipost |
|
A significant increase in identification rates occurred after introduction of the stamp, but there was no change when education was added. |
Screening, Identification, and Detection of Intimate Partner Violence
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
ED staff, including physicians, residents, interns, and nurses (Roberts et al., 1997a) |
Type: Unclear (workshops and case presentations) Length: Unclear Clinical aids: None Number of participants: Unclear |
|
Cohort |
% of self-reported IPV victims who were noted as such on chart within 24 hours after presentation |
Chart review |
|
ED, critical care, and perinatal hospital staff (Short et al., in press) |
Type: Length: Clinical aids: Protocol |
Usual and available |
Two groups (one comparison group) |
% of cases with documentation of definite IPV |
Chart review |
|
% of cases with documentation of suspected IPV |
Chart review |
||||
|
ED nurses (Tilden & Shepherd, 1987) |
Type: Didactic Length: 4 hrs. Clinical aids: Protocol and forms Number of participants: 22 |
|
Cohort |
% of all cases identified as IPV |
Chart review |
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
Yes |
12 |
|
Pre = 141 Post = 183 |
|
Ipost =Cpost |
Low attendance at training and lack of social work referral services at times when victims showed in the emergency room may have contributed to the lack of differences. |
|
|
|
15 |
18 21 24 |
Post = FU1 = FU2 = FU3 = |
Post = FU1 = FU2 = FU3 = |
|
IFU3 > CFU3* |
A total of 2,531 charts were reviewed, but the numbers were not reported for each data collection wave. |
|
IFU3 > CFU3* |
|||||||
|
Yes |
4 |
|
Pre = 447 Post = 445 |
|
Ipost >Ipre* |
|
|
Screening, Identification, and Detection of Intimate Partner Violence
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
Maternity care coordinators in county health departments (Covington et al., 1997a) |
Type: Didactic Length: Unclear Clinical aids: Protocol Number of participants: |
|
Cohort |
% of pregnant adolescents reporting IPV at first visit |
Self-report of adolescent patients |
|
% of pregnant adolescents reporting IPV at any visit |
Self-report of adolescent patients |
||||
|
Maternity care coordinators in county health departments (Covington et al., 1997b) |
Type: Didactic Length: Unclear Clinical aids: Protocol Number of partcipants: Unclear |
|
Cohort |
% of pregnant adult clients reporting IPV at first visit |
Self-report of pregnant patients |
|
% of pregnant adult clients reporting IPV at any visit |
Self-report of pregnant patients |
||||
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
Yes |
12 |
|
Pre = 129 Post = 117 |
|
Ipost >Ipre |
|
Analyses controlled for differences in race/ethnicity between the two patient cohorts. Although the rate of identification at the first visit doubled between baseline and the posttest, this was not a statistically reliable difference due to the small sample size. |
|
Ipost >Ipre* |
|||||||
|
Yes |
12 |
Pre = 1,056 Post = 384 |
Ipost >Ipre* |
Analyses controlled for differences in race/ethnicity and age between the two patient cohorts. The baseline review of charts covered a 36-month time span, and no differences were found in identification rates among the three years. |
|||
|
Ipost >Ipre* |
|||||||
Screening, Identification, and Detection of Intimate Partner Violence
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
Community health center staff, including physicians, mid-level practitioners, social workers, and psychologists (Harwell et al., 1998) |
Type: Mixed Length: 3-6 hrs. Clinical aids: IPV screening pocket card; IPV assessment form; stamp to indicate screening and suspected or confirmed abuse; patient card of resources and safety tips; additional tailored followup training to some CHCs Number of participants: 108 |
|
Cohort |
% of cases screened for IPV |
Chart review |
|
% of cases where IPV was suspected |
Chart review |
||||
|
% of cases where IPV was confirmed |
Chart review |
||||
|
Public health nurses (Shepard et al., 1999) |
Type: Mixed Length: 4 hrs. Clinical aids: Protocol Follow-ups Number of participants:12 |
Cohort |
% of cases identified as IPV |
Chart review |
|
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
Yes |
6 |
|
Pre = 251 Post = 255 |
|
Ipost >Ipre* |
|
There was no significant change in positive identification of IPV victims in the chart. |
|
Ipost >Ipre* |
|||||||
|
Ipost >Ipre |
|
||||||
|
Yes |
12 |
24 |
Pre = 546 Post = 442 FU = 372 |
|
Ipost >Ipre IFU1 >Ipre |
|
Differences in identification rates were not significant when age was controlled (although they were marginally significant). |
Screening, Identification, and Detection of Intimate Partner Violence
|
|
Nature of Training Provided |
Expected Outcomes and Measure |
|||
|
Target Population (study citation) |
Intervention Group |
Comparison Group (if applicable) |
Study Design |
Major Outcomes |
Measure |
|
Primary care team members (Thompson et al., 2000) |
Type: Mixed Length: 2 half-day sessions over 12 months Clinical aids: Posters; provider cue cards; routine exam forms; feedback |
Usual and available training (e.g., manual) |
Two groups (group randomized) |
% asking about IPV |
Provider self-report (one item) |
|
% of patients who were asked about IPV |
Chart review |
||||
|
% of patients who were victims of IPV |
Chart review |
||||
|
Prenatal health clinic staff, including physicians, nurses, nutritionists, counselors, and clerical staff (Wist & McFarlane, 1999) |
Type: Didactic Length: 90 min. Clinical aids: Protocol; follow-up |
No protocol in one clinic |
Two groups (one comparison group) |
% of patients identified as IPV |
Chart review |
|
Timing |
Sample Size and Attrition from Measurement |
Results I = Intervention Group C = Comparison Group Pre = Baseline or Pretest Post = Posttest FU = Follow-up |
|||||
|
Baseline |
Posttest (months) |
Follow-ups (months) |
Intervention |
Comparison |
Within-Group Change |
Relative Group Difference |
Comment |
|
Yes |
9 |
|
2 clinics Eligible = ? Pre = Post = 91 |
3 clinics Eligible = ? Pre = Post = 88 |
Ipost >Ipre* |
Ipost > Cpost* IFU >CFU Ipost > Cpost* |
Differences in recorded asking occurred among those who had physical exams and screening questionnaire. |
|
Ipost >Ipre* |
|||||||
|
Yes |
|
Pre = 1,590 Post = 1,372 Same |
Pre = 2,205 Post = 2,020 Same |
|
|||
|
Yes |
|
Ipost >Ipre |
Ipost >Cpost |
|
|||
|
Yes |
3 |
15 |
Pre = 360 Post = 110 FU2 = 250 |
Pre = 180 Post = 55 FU2 = 125 |
I(post+FU) > |
IFU >CFU* Ipost > Cpost* |
The percent of charts at the intervention site that contained an abuse screen declined from 95% at the 3-month posttest to 85% at the 15-month follow-up. |