Dolores One: Maximizing Functional Communication for Adults

Communication Clinical Trial

Official title: Dolores One: Maximizing Functional Communication for Adults Using Non-Invasive Ventilation in the Acute Care Setting

Status Withdrawn

Clinical Trial Summary

Difficulties with communication for patients requiring mechanical ventilation is known to be a source of distress in the acute care setting. The inability to speak has been associated with increased psychological distress and increased feelings of fear and anger and impact negatively on patient participation with caregivers and their overall recovery. Developing and maintaining communication between patients and hospital staff reduces patient stress and increases patient satisfaction and part of the standard pf care. According to the new and revised The Joint Commission standards, hospitals must identify and document patients' communication needs and communicate with patients during their care in a manner that meets those needs. Using the Dolores One device for patients can improve the ease and efficiency of communication while they are in the acute care setting. For non-speaking patients, nonverbal communication means are often used, including mouthing words and head nods to indicate yes/no responses. However, relying completely on nonverbal means can limit patient responses and lead to ineffective and frustrating communication exchanges. There have been several studies reviewing the negative effects of the inability to speak for intubated, mechanically ventilated patients. However, there is a need for more research to address communication difficulties in other mechanically ventilated populations, including patients receiving non-invasive ventilation and ventilator dependent tracheostomy patients. The Dolores One is comprised of an acoustic throat sensor and positioned at the patient's neck with a soft adjustable collar. The sensor gathers vocal cord vibrations and transmits signals to a control unit, processes the sensor signal, and finally, generates the patient's voice. The smart signal processing automatically accommodates both weak forced voices and whispers, producing a voice output to allow for normal conversation in a patient's natural voice, free from the sounds of rushing air or equipment noises secondary to Non-Invasive Mechanical Ventilation (NIMV) systems. The purpose of the study is to determine if the Dolores One devices can be used in the clinical acute care setting with patients in NIMV to improve their ability to communication as measured as ease to communicate and intelligibility, with family and the members of the medical team.

Clinical Trial Description

Primary Aims: 1. Is to determine if the Dolores One device can significantly improve the ease of communication as measured by the Ease of Communication 2. Is to determine if the Dolores One device can significantly improve the intelligibility of communication as measured by the Intelligibility section of the Frenchay Dysarthria Assessment (FDA). Design: This study will be a prospective study using a convenient cohort of 55 adult patients, who was using NIMV, to pilot the effectiveness of the Dolores One to improve verbal communication. There will be no randomization and no control group. The design is a pretest / posttest mixed method in which the Easy of Communication Scale and the Intelligibility section of the FDA will be administered at base line and repeated once the Dolores One has been set up on the patient. Methodology: The respiratory therapists who are working in the Medical Intensive Care Unit (MICU) and 10 West will complete the initial screening for potential subjects based upon the study's eligibility criteria. The floor respiratory therapist will notify the Principle Investigator (PI) of a potential subject. The PI will either verify that the patient meets the eligibility criteria or will contact another member of the study team to verify eligibility, medically appropriateness to participate and consent the patient. To screen for medical appropriateness and minimize risk a member of the study team will have a conversation with medical team to determine medical stability as defined as patient having stable vitals on NIMV as defined by medical team parameters and nursing orders for the individual patient and on stable NIMV setting for 30 to 90 minutes as per respiratory therapy guidelines. Once the consent has been obtained, the Speech Language Pathologist (SLP) will be notified and will obtain the data regarding the parameters of the NIMV and document current vital signs, which is standard practice for patient safety. Then the speech therapist will complete the baseline communication assessment using the Ease of Communication Scale and the Intelligibility section of the FDA. The Ease of Communication Scale is a self report 10 item questionnaire in which the subject rates their ability to communication while on NIMV. It is on a 5 item Likert scale and a total sum is recorded. For the Intelligibility Section of the FDA, the speech therapist will use a random table to select 5 short sentences or phrase in which there is a key word. The speech therapist will ask the subject to speak these phrase out loud. A volunteer staff member, who is unfamiliar with the list of possible sentences provided in the FDA, will be asked to write down the sentences the subject speaks. The SLP will score the intelligibility as a yes no response based upon the accuracy of the key word. Intelligibility will be reported as a percentage of correct responses. The statements will be randomized to decrease familiarity as well as there are over 140 nurses and 15 nurse aides and other various staff that work on these units that the speech therapist may obtain to as a volunteer. The volunteer pool is sufficient to decrease the likelihood of the volunteer being familiar with the statements to bias the test results. If a staff member who is assigned for daily care for this subject is unavailable, or unable to volunteer at time of testing, the Speech therapist will ask another staff member of the unit who has been educated regarding the study, to assist. After preliminary data collection has been completed, the SLP will place the Dolores One on the patient and adjust sensor position and device volume to achieve optimal voice output. The SLP will position the Dolores One on either side of the neck to assure comfort and effective sound. It will not be applied to any area of skin rash or lesion. The device can be removed at any time and reapplied when the patient would like to speak. The Dolores One will be left with the patient to have the opportunity to use the device to communicate with their health care team and visitors for the next 24 to 36 hours. The speech therapist training session will take approximately 10 minutes to train the subject on the use and to practice prior to the therapist leaving. The SLP will return between 24 and 36 hours from initial data collection, verify medical and NIMV stability, record vitals, obtain NIMV parameters, and repeat the Ease of Communication Scale and the Intelligibility Section of the FDA. After testing, this concludes the subjects participation in the study. Other data that will be collected include, age, race, gender, unit location, NIMV Manufacture brand, NIMV setting: Fraction of Oxygen (FiO2), Positive End Expiratory Pressures (PEEP), inspiratory pressure, minute ventilation, and patient vitals (heart rate, blood pressure, respiratory rate and oxygen saturation), leak percentage , and primary diagnosis. This data will be collected at the time pre and post application of the Dolores One prior to completing the Ease of Communication Survey and the Intelligibility Section of FDA. Prior to the start of this study the unit will receive education regarding the study and the general use of the Dolores One. Providers will be notified by providing educational materials in the team report rooms and will notify the attending as well as the medical director for the units Separate training regarding the study, use of the Dolores One and screening criteria will be given to the respiratory therapy department via their hand off meetings. This has been approved by respiratory leadership. The Respiratory Therapist (RT) will be provided with the eligibility criteria to improve screening process. ;

Related Conditions & MeSH terms

• Communication

• NCT number: NCT03934619
• Study type: Interventional
• Source: University of Maryland, Baltimore
• Status: Withdrawn
• Phase: N/A
• Start date: October 7, 2019
• Completion date: March 31, 2020