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1.
J Surg Res ; 263: 5-13, 2021 07.
Article in English | MEDLINE | ID: mdl-33618218

ABSTRACT

BACKGROUND: Few studies examine how residents can optimize their educational experience in the OR on their terms. This study aimed to examine residents' perceptions of how learners can maximize their education in the OR. METHOD: Using constructivist grounded theory methodology, the authors conducted focus groups with general surgery residents, PGY1-5, followed by semi-structured interviews with attending surgeons from a single, academic medical center. Constant comparison was used to identify themes and explore their relationships. Theoretical sampling was used until saturation was achieved. RESULTS: Residents and attendings participated. Two phases of OR learning were identified, intra-operative and inter-operative. Characters that made optimized learning included control, struggling, and reflection. Residents who practiced self-reflection with their experiences, and were able to articulate this awareness to attendings, felt the OR was an ideal learning environment. Attendings echoed similar findings. CONCLUSIONS: Providing residents with a method of maximizing OR learning is critical to postgraduate clinical education. Currently, observation passively morphs into active learning and eventually independent operating in the OR. However, residents who practice self-regulated learning, and are able to discuss their educational goals with attendings, seem to find the OR a better learning environment and progress to independence more quickly. This was echoed by practicing attendings. Providing residents with a generalizable, self-regulated learning framework specific to operative educational experiences could maximize learning potential and expedite resident progression in the OR.


Subject(s)
Internship and Residency/methods , Operating Rooms , Problem-Based Learning/methods , Surgeons/education , Surgical Procedures, Operative/education , Achievement , Clinical Competence , Focus Groups , Goals , Grounded Theory , Humans , Models, Educational
2.
BMC Med Res Methodol ; 4: 23, 2004 Oct 01.
Article in English | MEDLINE | ID: mdl-15458571

ABSTRACT

BACKGROUND: In most recent large efficacy trials of barrier contraceptive methods, a high proportion of participants withdrew before the intended end of follow-up. The objective of this analysis was to explore characteristics of participants who failed to complete seven months of planned participation in a trial of spermicide efficacy. METHODS: Trial participants were expected to use the assigned spermicide for contraception for 7 months or until pregnancy occurred. In bivariable and multivariable analyses, we assessed the associations between failure to complete the trial and 17 pre-specified baseline characteristics. In addition, among women who participated for at least 6 weeks, we evaluated the relationships between failure to complete, various features of their first 6 weeks of experience with the spermicide, and characteristics of the study centers and population. RESULTS: Of the 1514 participants in this analysis, 635 (42%) failed to complete the study for reasons other than pregnancy. Women were significantly less likely to complete if they were younger or unmarried, had intercourse at least 8 times per month, or were enrolled at a university center or at a center that enrolled fewer than 4 participants per month. Noncompliance with study procedures in the first 6 weeks was also associated with subsequent early withdrawal, but dissatisfaction with the spermicide was not. However, many participants without these risk factors withdrew early. CONCLUSIONS: Failure to complete is a major problem in barrier method trials that seriously compromises the interpretation of results. Targeting retention efforts at women at high risk for early withdrawal is not likely to address the problem sufficiently.


Subject(s)
Contraception Behavior , Nonoxynol/administration & dosage , Refusal to Participate/statistics & numerical data , Research Subjects/classification , Spermatocidal Agents/administration & dosage , Adult , Coitus , Female , Humans , Longitudinal Studies , Motivation , Nonoxynol/pharmacology , Pregnancy , Pregnancy Tests , Refusal to Participate/psychology , Reproducibility of Results , Research Design , Research Subjects/psychology , Risk , Spermatocidal Agents/pharmacology , Student Health Services , United States
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