Investigation of a Free Water Protocol

NCT ID: NCT06309602

Last Updated: 2025-06-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

136 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-10-22

Study Completion Date

2028-01-01

Brief Summary

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Hypothesis: Use of a Free Water Protocol (FWP) will improve patient satisfaction scores (Dysphagia Handicap Index), will not increase the risk of aspiration pneumonia/pneumonitis, and will result in improved oral hygiene (as assessed by the Oral Assessment Guide). Aim: To demonstrate that improvement in patient satisfaction and quality of life scores outweighs the potential risks of aspiration of plain water in an acute care setting; to qualitatively assess the implementation of a Free Water Protocol from the viewpoints of the patient and family/caregivers; to quantify changes in oral hygiene practices for individuals on the Free Water Protocol.

Detailed Description

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Individuals who have difficulty swallowing thin liquids are commonly restricted from ingesting plain water and prescribed a thickened liquid only diet to prevent choking hazards and aspiration pneumonia. These thickened liquids are intended to reduce aspiration of oral secretions carrying respiratory pathogens, the primary cause of aspiration pneumonia. This restriction from plain water (also known as thin water) can result in lowered patient satisfaction in addition to dissatisfaction with the texture and taste of thickened liquids. However, prior research from inpatient rehabilitation settings has demonstrated that plain water can be given to patients who otherwise require thickened liquids to prevent aspiration pneumonia. If patients prescribed a thickened liquid diet are allowed access to plain water, then hydration status may improve along with increased patient satisfaction.

This Free Water Protocol (FWP) differs from a thickened-liquids-only protocol in three ways: 1) allowing individuals access to plain, un-thickened water; 2) purposefully providing oral care prior to access of plain water; and 3) not allowing plain water until 30 minutes after meal completion and oral care has been completed with the intent to reduce the risk of pulmonary complications. Although many institutions have adapted and implemented an FWP, only 10 studies have measured pulmonary complications of an FWP. Among those, other outcomes are reported inconsistently with varying methodologies (e.g., fluid intake, hydration status, occurrences of urinary tract infection, satisfaction measures). More research is needed to demonstrate the benefits of allowing free water over the risk of potential pulmonary complications, especially in an acute care setting.

Conditions

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Oropharyngeal Dysphagia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Control / Standard Care

Standard care provided for patients with orders for thickened liquids.

Group Type OTHER

Control / Standard Care

Intervention Type OTHER

Standard care will be given to patients with orders for thickened liquids. This will include oral care twice a day and implementation of swallowing strategies and precautions as prescribed by the treating speech-language pathologist. Only fluids thickened to the recommended viscosity will be available to the patient.

Free Water Protocol

Standard care provided for patients with orders for thickened liquids. Additionally, participant will be allowed to have plain, un-thickened water after the following have taken place: 1) Wait 30 minutes after meal or medication administration; 2) Complete oral care according to instructions posted at bedside.

Group Type EXPERIMENTAL

Free Water Protocol

Intervention Type OTHER

Intake of plain, un-thickened water is allowed even when a patient has orders for thickened liquids. Risks of pulmonary complications are decreased with use of a strict oral care regimen and timed intake of water related to meals. Patient satisfaction and comfort is increased with ingestion of plain water.

Interventions

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Free Water Protocol

Intake of plain, un-thickened water is allowed even when a patient has orders for thickened liquids. Risks of pulmonary complications are decreased with use of a strict oral care regimen and timed intake of water related to meals. Patient satisfaction and comfort is increased with ingestion of plain water.

Intervention Type OTHER

Control / Standard Care

Standard care will be given to patients with orders for thickened liquids. This will include oral care twice a day and implementation of swallowing strategies and precautions as prescribed by the treating speech-language pathologist. Only fluids thickened to the recommended viscosity will be available to the patient.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Stroke diagnosis or trauma patients being cared for by Trauma \& Acute Care Surgery (TACS) providers
* Current orders for restricted or thickened liquids
* Ability to control their own airway (i.e. airway adjuncts not needed)

Exclusion Criteria

* Individuals who are medically fragile, as determined by treating physician, to include diagnosis of sepsis, need for vasopressors, or high oxygenation needs (requiring high-flow nasal cannula, Airvo, or oximask)
* Individuals who refuse oral care, have any decayed teeth or dental disease, or have a documented active oral infection
* Individuals with an advanced progressive neurological condition, active head/neck cancer, or those who are immunosuppressed
* Individuals who are on bed-rest orders
* Individuals who are lethargic or sedated
* Individuals with suspected pre-hospital aspiration event and/or aspiration pneumonitis
* Individuals with a fever of unknown origin
* Individuals with a history of recurrent aspiration pneumonia/pneumonitis
* Individuals whose primary language is one that the questionnaires are not available in a validated format
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Poudre Valley Health System

OTHER

Sponsor Role lead

Responsible Party

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Emily Main, MS, CCC-SLP

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Medical Center of the Rockies

Loveland, Colorado, United States

Site Status NOT_YET_RECRUITING

Medical Center of the Rockies

Loveland, Colorado, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Emily Main, MS

Role: CONTACT

970-624-4369

Facility Contacts

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Emily Main, MS, CCC-SLP

Role: primary

970-624-4369

Emily Main, MS

Role: primary

970-624-4369

Other Identifiers

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22-0465

Identifier Type: -

Identifier Source: org_study_id

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