Electrolarynx for Enabling Communication in the CHrOnically Critically Ill (EECCHO)

Communication Clinical Trial

— EECCHO  

Official title:

Feasibility Assessment of the Electrolarynx for Enabling Communication in the

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05604079
• Other study ID #: TorontoEGH
• Status: Completed
• Phase: N/A
• Start date: November 2014
• Est. completion date: December 2017

Study information

• Verified date: May 2021
• Source: Michael Garron Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

All critically ill patients receiving mechanical ventilation experience a period of inability to speak due to the need for cuffed endotracheal or tracheostomy tubes. Consequences of the inability to speak include: significant emotional distress; unrecognized pain; sleeplessness; increased use of restraints, self-extubation and line removal, as well as injury to self and healthcare professionals. Communication methods such as word mouthing, gesticulating, and writing may be ineffective and result in frustration. Recent technological innovations include communication boards and electronic speech generating devices however these require fine motor skills and coordination which may not be intact in the chronically critically ill. The Electrolarynx was recently shown to be effective in establishing communication in a case study of an intubated patient. Despite the well-recognized deleterious consequences of speech incapacity, few studies have evaluated communication strategies in the critically ill and no published study has evaluated the Electrolarynx in this patient population.

In this study, the investigators aim to assess the feasibility and patient acceptability of establishing speech with an Electrolarynx for intubated or tracheostomized patients experiencing difficult weaning and unable to tolerate cuff deflation. Feasibility will be determined by the proportion of participants able to produce intelligible and comprehensible speech. The investigators will also collect data on consent rates, reasons for refusal, the proportion of eligible patients and the time required for research procedures to inform future studies. The investigators will provide participants with a maximum of five Electrolarynx training sessions. On completion the investigators will measure speech intelligibility, comprehensibility, and patient acceptability using the Assessment of Intelligibility of Dysarthric Speech and the Ease of Communication scale. Satisfaction with communication and anxiety will be measured before and after Electrolarynx training. To the investigators' knowledge, this study will be the first to rigorously evaluate, using previously validated measures, the feasibility of the Electrolarynx for establishing communication for mechanically ventilated patients.

Description:

Despite the well-recognized deleterious consequences of speech incapacity, few studies have evaluated communication strategies for patients unable to tolerate cuff deflation. Despite the aforementioned case reports, no studies report the feasibility of the Electrolarynx in restoring communication. Communication impairment during hospitalization has implications for the quality and safety of care as it is a modifiable risk factor for adverse events. This has led to accreditation organizations mandating reasonable efforts to establish alternative communication strategies for patients unable to speak. For chronically critically ill (CCI) patients, inability to speak increases anxiety, decreases a sense of control, and impairs meaningful patient involvement in decision making. Anxiety can exacerbate pain, which is known to impede ventilator weaning. Therefore it is likely that the inability to speak can impact negatively on weaning outcomes. To the investigators' knowledge, this study will be the first to rigorously evaluate, using previously validated measures, the feasibility of the Electrolarynx for establishing communication for mechanically ventilated patients.

Overall Program of Research Hypothesis The investigators hypothesize that restoration of communication using the Electrolarynx can reduce patient anxiety resulting in improvement in weaning outcomes (weaning success and duration) and reduced adverse events associated with inability to communicate such as agitation, delirium, restraint use, and tube/line/device removal. Before being able to test this hypothesis, the feasibility of use of the Electrolarynx needs to be confirmed.

Study Aim The aim of this study is to assess the feasibility of establishing speech with an Electrolarynx for patients receiving ventilation via an endotracheal tube or tracheostomy experiencing difficult weaning and unable to tolerate cuff deflation. Feasibility will be determined in terms of the proportion of participants able to produce intelligible and comprehensible speech as well as ease of, and satisfaction with communication.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 24
• Est. completion date: December 2017
• Est. primary completion date: December 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 100 Years

Eligibility

Inclusion Criteria:

1. endotracheal tube or tracheostomy in situ and unable to tolerate cuff deflation for > one hour

2. alert, awake and able to follow simple commands demonstrated by a Glasgow Coma Score of 15 with the verbal score assigned for the ability to communicate words using non-vocal methods

3. able to read and understand English

4. = 18 years old

5. unimpaired oral-motor capabilities (functional speech structures) assessed by standard oral-peripheral examination by a speech language pathologist and capable of mouthing words in response to orientation questions

6. meets all the above criteria and is anticipated to require mechanical ventilation for a further 5 days

7. consent to participate..

Exclusion Criteria:

1. pre-existing hearing or speech impairment that seriously interferes with communication before hospitalization (as documented in chart or reported by family members)

2. previous diagnosis of dementia identified in the patient's medical history.

Related Conditions & MeSH terms

• Communication

Intervention

Device:
• Electrolarynx
The device transmits electronic sound source vibrations through soft tissue, either the neck at the level of the glottis, or less commonly the check. Speech is created through movements of articulators including the lips, tongue and jaw.

Locations

Country	Name	City	State
Canada	Saint Michael's Hospital	Toronto	Ontario
Canada	Sunnybrook Health Care Centre	Toronto	Ontario
Canada	Toronto East General Hospital	Toronto	Ontario

Sponsors (3)

Lead Sponsor	Collaborator
Michael Garron Hospital	Sunnybrook Health Sciences Centre, Unity Health Toronto

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Feasibility of the Electrolarynx for establishing successful communication defined as the ability to generate speech that is intelligible and comprehensible	We determined speech intelligibility and comprehensibility using the Assessment of Intelligibility of Dysarthric Speech (AIDS), a validated objective tool for quantifying single-word and sentence intelligibility. Intelligible speech was arbitrarily defined as =70% of words identified correctly by raters. Ability to establish comprehensible speech was defined as a difficulty score of = 5 averaged over the five sentences.	Within 5 days of training
Secondary	Perceived ease and satisfaction with use	The investigators will use a simplified form of the Ease of Communication scale developed by Menzel that has been adapted and used in studies assessing communication in non-vocal ICU patients. We will use a 5-point Likert type scale to measure satisfaction with 1 indicating very satisfied and 5 indicating not at all satisfied.	Within 5 days of training
Secondary	Training time	The investigators will record the total time spent to train each participant to use the Electrolarynx	Commencement and completion of training - training is a maximum of five days
Secondary	Anxiety	The investigators will measure anxiety using the Faces Anxiety Scale	Within 5 days of training
Secondary	Consent rate	The investigators will document the number of participants that consent and decline	One month after completion of study recruitment
Secondary	Time to complete research measures	The investigators will record the time to complete all research procedures	One month after completion of study recruitment
Secondary	Effectiveness of the Electrolarynx	The investigators will measure the effectiveness of the Electrolarynx for communication using the Electrolarynx Effectiveness Score	Within 5 days of training