Nursing Care Bundle on Oral Intake Among Critically Ill Children With Post-Extubation Dysphagia

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age6-18
SponsorKafrelsheikh University

About this trial

the aim of this study is to evaluate the effect of Nursing care Bundle on Oral Intake among Critically Ill Children with Post-Extubation Dysphagia

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

undergoing emergency oral endotracheal intubation for at least 48 hours

able to communicate and having no sensory deficit and accepted to participate in the research

Disqualifiers

children who had a history of neuromuscular disease, preexisting swallowing problems and agitated children were excluded.

Trial design

Design model

Parallel

Treatments tested in this trial

  • a nursing care bundle on oral intake

    Procedure/Surgery

    a nursing care bundle on oral intake will be started the day after their successful extubation and extend for 14th days. Additionally, the participants will be provided with a brief education on safe swallowing.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Conventional care groupNo intervention 0 interventions
Group B: Care bundle groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Change from baseline of oral health post-extubation on Post-Extubation Oral Assessment Scale

It consisted of eight categories including Voice, ability to swallow, lips, saliva, tongue, mucous membranes, gingiva and teeth. scoring of each component 0 score indicates (normal) , 1 score indicates (mild abnormality) and 2 scores indicate (sever abnormality). Total score (0-3) indicates minimal risk of post-extubation complications ,4-6 indicates moderate risk of complications and 7-10 indicates high risk of post-extubation complications.

Time frame
The first measurement time will be From extubation of mechanical ventilation up to 1 week"7 th day's post-extubation". The second time will be from extubation up to 2 week"14th day's" post-extubation
2

change from the baseline in swallowing on Pediatric Dysphagia Screening Questionnaire (PDSQ)

it designed to identify children at risk for oropharyngeal dysphagia. scoring of each component 0 score indicates (no difficultly) ,1 score indicates (mild difficulty)2 scores (moderate difficulty) and 3 score indicates (severe difficulty). Total score (0-5) indicates minimal or to no dysphagia risk ,6-10 indicates to some dysphagia risk, 11-15 indicates high dysphagia risk and 16-18 indicates Severe dysphagia risk.

Time frame
The first measurement time will be From extubation of mechanical ventilation up to 1 week"7 th day's post-extubation". The second time will be from extubation up to 2 week"14th day's" post-extubation
3

change from baseline of normal oral intake of the children on the Pediatric Functional Oral Intake Scale (P-FOIS)

it includes a 6-point scale used to assess a child's oral intake ability. It categorizes intake into seven levels, ranging from complete dependence on non-oral feeding to successful oral intake.

Time frame
The first measurement time will be From extubation of mechanical ventilation up to 1 week"7 th day's post-extubation". The second time will be from extubation up to 2 week"14th day's" post-extubation

Secondary outcomes

Other outcomes

Sponsors and contacts

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