Discomfort During Intravenous Cannulation in an Emergency Department: Impact of Communication

NCT ID: NCT03502655

Last Updated: 2020-07-07

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 251 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-12-13
• Study Completion Date: 2019-12-15

Brief Summary

The main goal of this study is to investigate whether the communication between patients and healthcare providers has an impact on pain and anxiety induced by the insertion of a peripheral venous catheter in an emergency department. Another goal is to determine if the effect is mediated by the content of the message in itself or if it is mediated by non-verbal cues . Therefore, the message will be delivered by either an audio recording in the first phase of the study, and by the healthcare providers themselves in the second phase of the study. A secondary goal is to assess whether there are discrepancies between the patients' pain and anxiety reports and the healthcare providers' evaluation of the patient's pain and anxiety.

Detailed Description

A medical or surgical emergency is a stressful life event. An emergency department is also a noisy and sometimes chaotic environment, contributing in itself to increase the anxiety related to the primary cause of the emergency consultation. Some common medical procedures, such as placing an intravenous catheter, may not only induce pain, but may exacerbate patients' anxiety or pre-existing pain. The well-being of patients, especially during invasive medical procedures, can however be improved by various communication techniques. However, the medical literature and clinical observation have shown that negative words are traditionally used to warn patients of an impending painful stimulus. However, contrary to common beliefs and practices, this type of warning can increase pain and anxiety. Using words with negative emotional content has an even greater impact than the positive impact of using words with positive emotional content. However, studies that have explored the impact of such messages suffer from two limitations: first, they were not conducted in the context of emergency department, and second, the effect attributable to healthcare providers themselves was not studied. However, healthcare providers who deliver a message with a positive or negative content in the context of a study are not blinded to message, therefore are aware of the arm of the intervention. This lack of double-blinding may introduces a bias, namely that the benefit of a positive message can be linked to healthcare providers and their global interaction with patients, and not just to verbal content. of the message. It is indeed possible that the caregivers, in a more or less conscious way, add in their communication elements congruent with the message studied, whether in the field of verbal or nonverbal communication (tone of voice, warmth, empathy , etc.).

The purpose of this study is therefore to investigate whether the modulation of information relating to the setting up of a CIP in emergencies has an impact on patients' pain and their level of anxiety. It also seeks to determine if this effect is comparable, whether the message is delivered by a standardized audio recording or by caregivers. Finally, it aims to explore whether there are differences in the assessment of pain and anxiety made by patients and that made by caregivers.

Statistical analysis will be realized using the Stata software, version 14 (StataCorp, Tx, USA). Descriptive data will be presented by mean and standard deviation, median and interquartile space or proportions regarding continuous gaussian, non-gaussian and categorical variables. Comparison between randomized groups will be done by using non paired Student t-test or Wilcoxon rank sum test regarding continuous variables, and by Chi2 test or Fisher exact regarding categorical variables, according to what is appropriate.

This study aims to demonstrate the superiority of an informative message with positive content over pain perception during intravenous cannulation. Statistical power is set at 80% to prove a difference, with alpha threshold at 0.05. Mean pain intensity is estimated at 34 mm on a Visual Analog Scale (possible intensity from 0 to 100 mm), with an estimated standard deviation at 24 mm. To detect the smallest clinically significative decrease in pain intensity (13 mm) caused by the intervention, a sample of 110 patients, that is 55 patients per group, is needed. Taking missing data or post-randomization patient withdrawal (estimated at 10%) into account, 60 patients will be randomized per group. A minimum of 240 patients in total for the two phases (that is the four arms of the study) will be needed to be enrolled.

Conditions

Pain, Acute; Catheterization, Peripheral

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: QUADRUPLE

Study Groups

Intervention message (first phase)

Standardized message The intervention will consist in the delivery of a message with a positive content regarding the insertion of the peripheral venous catheter. The message will be delivered through an audio record

Group Type: OTHER

Experimental: Intervention message (first phase)

Intervention Type: OTHER

Effect of positive communication on pain during intravenous cannulation in an emergency department delivered by a recorded message

Control message (first phase)

Standardized message The intervention will consist in the delivery of a control message, whose content is based upon the usual caregiver-patient communication prior to the insertion of a peripheral venous catheter. The message will be delivered through an audio record.

Group Type: ACTIVE_COMPARATOR

Placebo Comparator: Control message (first phase)

Intervention Type: OTHER

Effect of usual communication on pain during intravenous cannulation in an emergency department delivered by a recorded message

Intervention message (second phase)

Standardized message The intervention will consist in the delivery of message with a positive content regarding the insertion of the peripheral venous catheter. The message will be delivered by the health providers themselves before inserting the catheter.

Group Type: OTHER

Experimental: Intervention message (second phase)

Intervention Type: OTHER

Effect of positive communication on pain during intravenous cannulation in an emergency department delivered by a care provider

Control message (second phase)

Standardized message In this arm, the patient will be delivered a control message, which content is based upon the usual caregiver-patient communication prior to the insertion of a peripheral venous catheter. The message will be delivered by the caregivers themselves before inserting the catheter.

Group Type: ACTIVE_COMPARATOR

Placebo Comparator: Control message (second phase)

Intervention Type: OTHER

Effect of usual communication on pain during intravenous cannulation in an emergency department delivered by a care provider

Interventions

Experimental: Intervention message (first phase)

Effect of positive communication on pain during intravenous cannulation in an emergency department delivered by a recorded message

Intervention Type: OTHER

Placebo Comparator: Control message (first phase)

Effect of usual communication on pain during intravenous cannulation in an emergency department delivered by a recorded message

Intervention Type: OTHER

Experimental: Intervention message (second phase)

Effect of positive communication on pain during intravenous cannulation in an emergency department delivered by a care provider

Intervention Type: OTHER

Placebo Comparator: Control message (second phase)

Effect of usual communication on pain during intravenous cannulation in an emergency department delivered by a care provider

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Patient aged 18 or more;
• Patient whose medical care requires a peripheral venous catheter;
• Insertion of the peripheral venous catheter on the upper limb.

Exclusion Criteria

• Patient clinically unstable;
• Patient incapable of discernment or with whom it is difficult to communicate (altered mental status, intoxication, alcoholized patient, insufficient French notions to give an informed consent and answer questions about pain and anxiety, hearing-impaired patient);
• Patient unable to correctly use the rulers (e.g. visually impaired patient);
• Impaired upper limb (e.g. lymphedema);
• Patient incarcerated;
• Patient transferred from another hospital;
• Patient who has already taken part in the study;
• Patient who knows beforehand that communication will be evaluated;
• Patient, caregiver or investigator who knows beforehand which message will be delivered (first phase of the study).

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Lausanne Hospitals

OTHER

Sponsor Role: collaborator

Olivier Hugli

OTHER

Sponsor Role: lead

Responsible Party

Olivier Hugli

Head of the inpatient service, Emergency Department

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Olivier Hugli, PD-MER, MPH

Role: PRINCIPAL_INVESTIGATOR

Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland

Locations

Centre Hospitalier Universitaire Vaudois (CHUV)

Lausanne, Canton of Vaud, Switzerland

Countries

Switzerland

References

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Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

VVP01112017

Identifier Type: -

Identifier Source: org_study_id