Intelligent Cooperation is Influenced by Learning Theories

April 14, 2021 updated by: University of Missouri, Kansas City
Qualitative Review of Intraoperative teaching and learning

Study Overview

Status

Withdrawn

Conditions

Detailed Description

From manuscript draft Methods:

2.1 Setting, Participants and Data Collection In this qualitative study the investigators examined authentic examples of intraoperative teaching exchanges between attending and resident surgeons. These examples were taken from two previous studies conducted at a large women's hospital: the objectives of those studies were to compare attending and resident responses regarding avoiding intraoperative errors[31] and to develop the previously mentioned Intelligent Cooperation framework.[10] The 10 surgical cases were gynecologic, representing open abdominal, laparoscopic, and vaginal approaches. Surgical cases were chosen by convenience, according to the schedule of the filmographer. Participants included ten surgical attendings, four fellows, and eleven Obstetrics and Gynecology residents, ranging from PGY1 to PGY4. the investigators conducted interviews with all ten attending surgeons and five of the residents. The data for this study included the case video, deidentified transcripts of the cases, and deidentified transcripts of the interviews. Our qualitative approach was most informed by Sandelowski's concept of developing rich qualitative descriptions.[32]

2.2 Research Team the investigators' interdisciplinary research team consisted of a female pelvic surgeon with twenty years of surgical teaching experience (GS), a medical education researcher and educational sociologist (LA), a neurosurgeon and administrator with 30 years of experience across the continuum of medical education (SK), and a cognitive psychologist with expertise in surgical education research (EBL).

2.3 Data Analysis the investigators reviewed and discussed the works of key sociocultural learning scholars, as described in our Introduction. The discussions were converted into a list of "key tenets" of the SCLTs, with associated examples from K-12 and Higher Education. (see Table 1) the investigators then independently coded all transcripts according to the key tenets and examples from our list, noting which exchanges reflected various sociocultural theories. Counting themes was not part of the methodological approach in this study because it was inconsistent with the intent of the study to develop deep, rich, and comprehensive insights about teaching in the OR.[33] the investigators subsequently met as a group to review coding, convert them into themes of teaching and learning advanced surgical skills, and select notable examples from our data. (see Table 2) These themes were then transformed into instructional strategies to improve surgical teaching, based on the sociocultural theories. (see Table 3) Disagreements were settled by group discussion. Data saturation was determined according to our study objective[34], to identify intraoperative instructional strategies related to the social cultural learning theories. the investigators stopped analyzing transcripts when the investigators had generated no new instructional strategies.

2.4 Reflexivity and Ethics During the meetings, the investigators maintained a reflexive atmosphere, reflecting on their backgrounds, experience, and biases and how those might affect their interpretation of the data. the investigators challenged those biases often. the investigators reached consensus regarding differences in data interpretation through group discussion. The University IRB approved this study as exempt.

Study Type

Observational

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

The films included ten surgical attendings, four fellows, and eleven Obstetrics and Gynecology residents, ranging from PGY1 to PGY4. We conducted interviews with all ten attending surgeons and five of the residents.

Description

Inclusion Criteria:

Films and transcripts from the database

Exclusion Criteria:

None: the investigators will consider all films and transcripts from the database

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Themes related to Surgical teaching and learning
Time Frame: approximately 1 year
Themes were derived by thematic analysis, as informed by Sandelowski's concept of developing rich qualitative descriptions
approximately 1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2018

Primary Completion (Actual)

April 10, 2021

Study Completion (Actual)

April 10, 2021

Study Registration Dates

First Submitted

April 11, 2021

First Submitted That Met QC Criteria

April 14, 2021

First Posted (Actual)

April 20, 2021

Study Record Updates

Last Update Posted (Actual)

April 20, 2021

Last Update Submitted That Met QC Criteria

April 14, 2021

Last Verified

April 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • 19-009

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Surgical Education

Clinical Trials on No Intervention - this was a qualitative analysis

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