Development and Validation of the SWADOC Tool

Sponsor
University of Liege (Other)
Overall Status
Recruiting
CT.gov ID
NCT04706689
Collaborator
Centre Hospitalier Universitaire de Liege (Other), Centre de Traumatologie et de Réadaptation de Jette (Erasme, ULB) (Other), Cliniques de Soins Spécialisés Valdor-Pèrî (Other), Centre Hospitalier Neurologique William Lennox (UCL) (Other), Centre Hospitalier Universitaire de Nīmes (Other), Uzès hospital (Other), Fontfroide functional re-education centre, Montpellier, France (Other)
104
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59.2
13
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Study Details

Study Description

Brief Summary

Background: After a period of coma, patients with severe brain injury may present disorders of consciousness (DOC). A wide proportion of these patients also suffer from severe dysphagia. Assessment and therapy of swallowing disabilities of DOC patients are essential because dysphagia has major functional consequences and comorbidities. Dysphagia evaluation in patients with DOC is hampered by the lack of adapted tools. The first aim of the study was to develop a new tool, the SWallowing Assessment in Disorders Of Consciousness (SWADOC), and propose a validation protocol. The SWADOC tool has been developed to help therapists to apprehend components related to swallowing in patients with DOC. The second aim is to appreciate the relationship between patients' level of consciousness and SWADOC items and scores.

Method/design: In this multicentric prospective cohort, 104 patients with DOC will be tested three times during two consecutive days with the SWADOC tool. Statistical analyses will focus on the reliability and validity of the SWADOC tool, especially the intra and inter-rater reliability, internal consistency, measures of dispersion and concurrent validity with the FOTT Swallowing Assessment of Saliva (FOTT-SAS). The level of consciousness will be assessed with the Simplified Evaluation of CONsciousness Disorders (SECONDs) and the Coma Recovery Scale-Revised (CRS-R)

Discussion: The assessment of swallowing abilities among patients with DOC is the first necessary step towards the development of an individualized dysphagia care plan. A validated scoring tool will be essential for clinicians to better apprehend dysphagia in DOC patients and to document the evolution of their disorders.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: SWADOC tool
  • Behavioral: FOTT-SAS

Study Design

Study Type:
Observational
Anticipated Enrollment :
104 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
The Development and Validation of the SWADOC Tool: A Study Protocol for a Multicentric Prospective Cohort Study
Actual Study Start Date :
Jul 24, 2020
Anticipated Primary Completion Date :
Dec 31, 2024
Anticipated Study Completion Date :
Jun 30, 2025

Arms and Interventions

Arm Intervention/Treatment
Unresponsive wakefulness syndrome patients (UWS)

The level of consciousness will be assessed with the Simplified Evaluation of CONsciousness Disorder (SECONDs) and the Coma Recovery Scale-Revised (CRS-R).

Behavioral: SWADOC tool
The tool explores some oral and pharyngeal components of swallowing as well as a range of prerequisite and related components of swallowing in DOC patients. It is composed of an average of 50 qualitative items and a subsection named "SWADOC-scored" comprising 8 quantitative items.

Behavioral: FOTT-SAS
Facial Oral Tract Therapy Swallowing Assessment of Saliva : the results of the SWADOC-scored in one of the sessions will be compared to the FOTT Swallowing Assessment of Saliva (FOTT-SAS) (27). The test is based on 7 questions under which if items 1-4 are answered "Yes" and items 5-7 are answered "No", oral intake should be initiated. The FOTT-SAS includes items that can be scored based on the administration of the SWADOC tool. In that respect, no additional administration will be required

Minimally conscious patients MINUS (MCS-)

The level of consciousness will be assessed with the Simplified Evaluation of CONsciousness Disorder (SECONDs) and the Coma Recovery Scale-Revised (CRS-R).

Behavioral: SWADOC tool
The tool explores some oral and pharyngeal components of swallowing as well as a range of prerequisite and related components of swallowing in DOC patients. It is composed of an average of 50 qualitative items and a subsection named "SWADOC-scored" comprising 8 quantitative items.

Behavioral: FOTT-SAS
Facial Oral Tract Therapy Swallowing Assessment of Saliva : the results of the SWADOC-scored in one of the sessions will be compared to the FOTT Swallowing Assessment of Saliva (FOTT-SAS) (27). The test is based on 7 questions under which if items 1-4 are answered "Yes" and items 5-7 are answered "No", oral intake should be initiated. The FOTT-SAS includes items that can be scored based on the administration of the SWADOC tool. In that respect, no additional administration will be required

Minimally conscious patients PLUS

The level of consciousness will be assessed with the Simplified Evaluation of CONsciousness Disorder (SECONDs) and the Coma Recovery Scale-Revised (CRS-R).

Behavioral: SWADOC tool
The tool explores some oral and pharyngeal components of swallowing as well as a range of prerequisite and related components of swallowing in DOC patients. It is composed of an average of 50 qualitative items and a subsection named "SWADOC-scored" comprising 8 quantitative items.

Behavioral: FOTT-SAS
Facial Oral Tract Therapy Swallowing Assessment of Saliva : the results of the SWADOC-scored in one of the sessions will be compared to the FOTT Swallowing Assessment of Saliva (FOTT-SAS) (27). The test is based on 7 questions under which if items 1-4 are answered "Yes" and items 5-7 are answered "No", oral intake should be initiated. The FOTT-SAS includes items that can be scored based on the administration of the SWADOC tool. In that respect, no additional administration will be required

Patients emerging from the minimally conscious state (EMCS)

The level of consciousness will be assessed with the Simplified Evaluation of CONsciousness Disorder (SECONDs) and the Coma Recovery Scale-Revised (CRS-R).

Behavioral: SWADOC tool
The tool explores some oral and pharyngeal components of swallowing as well as a range of prerequisite and related components of swallowing in DOC patients. It is composed of an average of 50 qualitative items and a subsection named "SWADOC-scored" comprising 8 quantitative items.

Behavioral: FOTT-SAS
Facial Oral Tract Therapy Swallowing Assessment of Saliva : the results of the SWADOC-scored in one of the sessions will be compared to the FOTT Swallowing Assessment of Saliva (FOTT-SAS) (27). The test is based on 7 questions under which if items 1-4 are answered "Yes" and items 5-7 are answered "No", oral intake should be initiated. The FOTT-SAS includes items that can be scored based on the administration of the SWADOC tool. In that respect, no additional administration will be required

Outcome Measures

Primary Outcome Measures

  1. Change in the SWADOC-scored during three sessions (Examiner 1) - Intra-reliability [15-25 minutes (3 times in 5 business days)]

    The SWallowing Assessment in Disorders Of Consciousness (SWADOC) tool is composed of an average of 50 qualitative and quantitative items. The subsection "SWADOC-scored" includes the 8 quantitative items. Four items are linked to the oral phase and four to the pharyngeal phase. For each quantitative item, patient's abilities are rated on a four-level severity scale ranging from 0 to 3. These levels correspond to item scores that can be added together to calculate 3 performance scores: the oral phase sub-score (sum of the 4 oral item scores - minimum of 0, maximum of 12), the pharyngeal phase sub-score (sum of the 4 pharyngeal item scores - minimum of 0, maximum of 12) and the total swallowing score (sum of the 8 item scores - minimum of 0, maximum of 24). The better the score is, the better the swallowing is.

  2. SECONDs [7 minutes (immediately before or after the SWADOC tool in each of the three sessions)]

    The Simplified Evaluation of CONsciousness Disorders (SECONDs): it features a shorter administration time (median of 7 minutes) and required only a mirror as material. It consists of 8 items: observation and reporting spontaneous behaviors, response to command, communication, visual pursuit and fixation, pain localization, oriented behaviors and arousal. The SECONDs provides a total score directly reflecting one diagnosis (0 = coma, 1 = UWS, 2-5 = MCS-, 6-7 = MCS+, 8 = EMCS). The better the score is, the better the consciousness level is.

Secondary Outcome Measures

  1. SWADOC-scored by Examiner 2 (inter-reliability) [15-25 minutes - immediately before or after one of the three sessions]

    The SWallowing Assessment in Disorders Of Consciousness (SWADOC) tool is composed of an average of 50 qualitative and quantitative items. The subsection "SWADOC-scored" includes the 8 quantitative items. Four items are linked to the oral phase and four to the pharyngeal phase. For each quantitative item, patient's abilities are rated on a four-level severity scale ranging from 0 to 3. These levels correspond to item scores that can be added together to calculate 3 performance scores: the oral phase sub-score (sum of the 4 oral item scores - minimum of 0, maximum of 12), the pharyngeal phase sub-score (sum of the 4 pharyngeal item scores - minimum of 0, maximum of 12) and the total swallowing score (sum of the 8 item scores - minimum of 0, maximum of 24). The better the score is, the better the swallowing is.

  2. FOTT-SAS (Examiner 1) [Immediately after one of the three sessions]

    FOTT-SAS (Facial Oral Tract Therapy Swallowing Assessment of Saliva) The FOTT-SAS is a reliable assessment for detecting aspiration risk in patients with acquired brain injury. The test is based on 7 questions under which if items 1-4 are answered "Yes" and items 5-7 are answered "No", oral intake should be initiated (the better the score is, the better the swallowing is, minimum of 0, maximum of 7). The observations made during the assessment will permit to score the FOTT-SAS and verify the concurrent validity of the SWADOC tool.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria :
  • Age above 18-year-old

  • Perfect knowledge of French language before the injury

  • Previous event of coma phase caused by a severe acquired brain injury

  • Medical stability (absence of mechanical ventilation and sedation, no acute medical pathology such as infection or respiratory distress)

  • No neurological or otorhinolaryngological disease which can impact swallowing prior to the brain injury

  • Minimum of 28 days since the acquired brain injury at inclusion

  • Diagnosis of UWS, MCS-, MCS+ or EMCS based on the CRS-R or SECONDs

  • Informed consent from legal representative of the patient

  • Affiliated patient or beneficiary of a health insurance plan (for French participants only).

Contacts and Locations

Locations

Site City State Country Postal Code
1 Centre Hospitalier Neurologique William Lennox (UCL) Ottignies-Louvain-la-Neuve Brabant Wallon Belgium 1340
2 Centre neurologique et de réadaptation fonctionnelle de Fraiture-en-Condroz Fraiture Belgium 4557
3 Centre de Traumatologie et de Réadaptation de Jette (Erasme, ULB) Jette Belgium
4 Centre du Cerveau², University Hospital of Liège Liège Belgium 4000
5 Cliniques de Soins Spécialisés Valdor-Pèrî Liège Belgium 4000
6 Fontfroide functional re-education centre Montpellier France
7 CHU Nîmes Nîmes France
8 Uzès hospital Uzès France

Sponsors and Collaborators

  • University of Liege
  • Centre Hospitalier Universitaire de Liege
  • Centre de Traumatologie et de Réadaptation de Jette (Erasme, ULB)
  • Cliniques de Soins Spécialisés Valdor-Pèrî
  • Centre Hospitalier Neurologique William Lennox (UCL)
  • Centre Hospitalier Universitaire de Nīmes
  • Uzès hospital
  • Fontfroide functional re-education centre, Montpellier, France

Investigators

  • Study Director: Olivia Gosseries, PhD, University of Liege, Giga Consciousness

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Olivia Gosseries, Neuropsychologist, PhD, Co-director of the Coma Science Group, Research Associate at FRS-FNRS, University of Liege
ClinicalTrials.gov Identifier:
NCT04706689
Other Study ID Numbers:
  • 2020_79
First Posted:
Jan 13, 2021
Last Update Posted:
Sep 29, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Olivia Gosseries, Neuropsychologist, PhD, Co-director of the Coma Science Group, Research Associate at FRS-FNRS, University of Liege
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 29, 2021