Impact Of The Nurse Enhanced Recovery After Surgery Coordinator On The Compliance In Colorectal Surgery (nursERAS-BCN)

Summary

Purpose. The aim of this study is to evaluate the impact of the implementation of the Nurse Enhanced Recovery After Surgery Coordinator (NEC), within the Enhanced Recovery After Surgery (ERAS) program, in relation to the compliance of patients undergoing colorectal surgery.

Methods. Quasi-experimental study with a control group, an intervention group and without random assignment in a multicenter trial; between December 2021 and November 2023. Patients older than 18 years with planned elective intervention of major colorectal surgery will be included; excluding those without social support, with psychiatric illness, cognitive difficulty, planning of simultaneous or emergency surgery. In the intervention arm they will have NEC and in the control group they will not have that resource. Compliance will be the main variable of the study and, in addition, the study aims to assess secondary endpoints such as quality of life (QOL).

Conclusions. NEC could increase compliance to ERAS programs, improving health outcomes and QOL perceived by the patient. The applicability in the different hospital centers could generate an opportunity to advance professionally in the nursing figure within the ERAS program. The fact of having NEC could also increase the efficiency of the program due to the cost-effectiveness of the nursing position, although this is not the object of the study. It would be applicable in improving perceived health and QOL, so it could also have an economic impact on the health system.

Conditions

• ERAS
• Enhanced Recovery
• Compliance, Treatment
• Compliance, Patient
• Nurse's Role
• Colon Disease
• Rectum Disease

Interventions

OTHER

Nurse Enhanced Recovery After Surgery participation

Bellvitge University Hospital will include the NEC participation along Enhanced Recovery After Surgery program.

Sponsors & Collaborators

• Germans Trias i Pujol Hospital

  collaborator OTHER

• University of Barcelona

  collaborator OTHER

• Hospital Universitari de Bellvitge

  lead OTHER

Principal Investigators

• Jose Antonio Jerez-Gonzalez, MSc · Hospital Universitari de Bellvitge

• M.Carmen Moreno-Arroyo, PhD · University of Barcelona

• Miguel Angel Hidalgo-Blanco, PhD · University of Barcelona

Study Design

Allocation

NON_RANDOMIZED

Purpose

SUPPORTIVE_CARE

Masking

NONE

Model

PARALLEL

Eligibility

Min Age

18 Years

Sex

ALL

Healthy Volunteers

No

Timeline & Regulatory

Start

2022-05-01

Primary Completion

2025-04-30

Completion

2025-04-30

Countries

• Spain

Study Locations