MedDataX Logo

Burnout Preventions, Professionalism Heightening, and Enhancing Resiliency (BUPHER)

NCT ID: NCT02963792

Last Updated: 2016-11-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

1000 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-11-30

Study Completion Date

2020-09-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Due to their difficult and stressful work surgeons are under continuous physical and mental stress exposing them to increased risk for burnout and lack of professionalism. The present intervention focuses on providing time and a safe space to debrief and explore personal and group experiences and dilemmas, as well as acquire coping skills related to burnout, communication and professionalism.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Professional-Patient Relations Burnout, Professional

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Professionalism Burnout prevention Resiliency Student education

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Structured group intervention

Experimental: Structured group intervention a 'structured' intervention, leaning mostly on tools designed to prevent burnout and promote resilience, including predetermined exercises and topics as discussion goals in each meeting.

Fidelity will be checked and monitored at the end of each meeting, when facilitators fill out a form that summarizes the content, topics and coping skills acquired in each session.

Group Type EXPERIMENTAL

Preventing Professionals burnout

Intervention Type OTHER

Semi-Structured group intervention

Experimental: Semi-Structured group intervention a 'semi-structured' intervention, based on tools for developing an emotional discourse, building a supporting team and self reflection.

The 'semi-structured' intervention offers predetermined contents that are discussed through the stories and needs presented by group members.

Fidelity will be checked and monitored at the end of each meeting, when facilitators fill out a form that summarizes the content, topics and coping skills acquired in each session.

Group Type EXPERIMENTAL

Preventing Professionals burnout

Intervention Type OTHER

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Preventing Professionals burnout

Intervention Type OTHER

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Enhancing professional professional conduct

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* All physicians (residents and experts) of the Surgical Division at Tel Aviv Sourasky Medical Center.
* All medical students studying at the Sackler Faculty of Medicine, Tel Aviv University, and attending a surgery round at the Surgical Division at Tel Aviv Sourasky Medical Center.
* Patients (and/or family members) in the Surgical Division at Tel Aviv Sourasky Medical Center following their surgery.

* non-Hebrew speaking patients;
* ventilated patients;
* patients in surgical intensive care;
* patients medically defined as suffering from clouding of conscious or delirium;
* subjects who decided to stop their participation in the study.

Exclusion Criteria

* The research will not include children and/or judgment-impaired patients;
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Association for Children at Risk

OTHER

Sponsor Role collaborator

Tel Aviv University

OTHER

Sponsor Role collaborator

michal roll

OTHER_GOV

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

michal roll

Principal of the department of surgery and the unit of surgical oncology

Responsibility Role SPONSOR_INVESTIGATOR

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Orit Karnieli-Miller, PhD

Role: CONTACT

Phone: +972502060619

Email: [email protected]

Nathaniel Laor, MD; PhD

Role: CONTACT

Phone: +972546441354

Email: [email protected]

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

TASMC-16-GL-0426-CTIL

Identifier Type: -

Identifier Source: org_study_id