Table 3.
Study | Study designb | Sampling (number of programs)c | Survey response rated | Types of outcomes measurese | Validity of evaluation toolsf | Data analysis appropriate?g | Data analysis strategyh | Reported outcome(s)i | Total quality scorea | |
---|---|---|---|---|---|---|---|---|---|---|
“Short” ambulatory blocks (1 week) | ||||||||||
Chaudry et al., 201324 | Pre-post | 1 | > 75% | Objective | Providedj | Appropriate | Beyond descriptive | Satisfaction, general facts | 11.5 | |
Harrison et al., 201425 | Non-randomized trial | 1 | > 75% | Self-assessed | Providedj | Appropriate | Beyond descriptive | Satisfaction, general facts | 10 | |
Heist et al., 201426 | Non-randomized trial | 1 | NA | Objective | NAk | Appropriate | Beyond descriptive | Behaviors | 10.5 | |
Mariotti et al., 201027 | Pre-post | 1 | 50–74% | Self-assessed | Providedj | Appropriate | Beyond descriptive | Satisfaction, general facts | 9 | |
Other ambulatory block designs | ||||||||||
Bates et al., 2016 23 | Pre-post | 1 | > 75% | Self-assessed | Providedj | Appropriate | Descriptive | Satisfaction, general facts | 8.5 | |
Francis et al. | June 201417 | Non-randomized trial | > 3 | > 75% | Self-assessed | Provided | Appropriate | Beyond descriptive | Satisfaction, general facts | 13 |
Sept 201418 | Non-randomized trial | > 3 | > 75% | Objective | Provided | Appropriate | Beyond descriptive | Patient health care outcomes | 17 | |
201519 | Non-randomized trial | > 3 | > 75% | Objective | Provided | Appropriate | Beyond descriptive | Satisfaction, general facts | 13.5 | |
201620 | Non-randomized trial | > 3 | NA | Objective | Provided | Appropriate | Beyond descriptive | Patient health care outcomes | 17 | |
Warm et al., 200828 | Pre-post | 1 | NR | Objective | Provided | Appropriate | Beyond descriptive | Patient health care outcomes | 14.5 | |
Wieland et al., 201329 | Pre-post | 1 | 50–74% | Objective | Provided | Appropriate | Beyond descriptive | Patient health care outcomes | 15 |
NA not applicable, NR not reported
aAssessed using the Medical Education Research Study Quality Instrument (MERSQI). The total possible score is 18. Green denotes higher methodologic quality, yellow denotes moderate quality, and orange denotes fair quality
bStudy design defined as post-test only (1 point), “pre-post” (one group compared before and after intervention; 1.5 points); “non-randomized trial” (separate concurrent control and intervention groups; 2 points), randomized control trial (3 points)
cPotential number of institutions is 1 (0.5 points), 2 (1 points), or ≥ 3 (1.5 points). Studies involving a greater number of institutions are considered higher quality
dSurvey response rate on post-test data; < 50% or not reported (0.5 points), 50–74% (1 point), ≥ 75% (1.5 points)
ePotential types of outcomes measures are assessment by a study participant (1 point), or objective (3 points)
fValidity of evaluation tools is defined as content validity or using existing tools (1 point), internal structure validity (1 point), and correlation with other variables (1 point)
gAppropriateness of data analysis is defined as analysis that was appropriate for the study design (1 point) or not appropriate for study design (0 point)
hData analysis strategy is defined as descriptive only (1 point) or beyond descriptive analysis (2 points)
iReported outcomes are defined as satisfaction, attitudes, perceptions, opinions, general facts (1 point), knowledge or skills (1.5 points), behaviors (2 points), and patient health outcomes (3 points)
jValidity was based on expert opinion only
kNo survey instruments were used in this study