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Clinical Evaluation of the Response to Chest Physiotherapy in Children With Acute Bronchiolitis

FIBARRIX Clinical Evaluation of the Response to Chest Physiotherapy in Infants With Acute Bronchiolitis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02458300
Acronym
FIBARRIX
Enrollment
77
Registered
2015-06-01
Start date
2015-01-31
Completion date
2015-03-31
Last updated
2016-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bronchiolitis

Keywords

Bronchiolitis, Chest, Physical therapy

Brief summary

The objective of this study is to evaluate the clinical response of children diagnosed with acute bronchiolitis, relative to a chest physiotherapy protocol. Comparing this treatment with standard care of the nursing staff and auxiliaries of infants patients aged 1 month to 2 years.

Detailed description

This randomized clinical trial has an intervention group and a control group. All treatment will be made by physiotherapist with extensive clinical experience and training in techniques of Chest physiotherapy (CPT). Performing at least one session per day during the time of patient admission. This session takes an average of about 15 minutes, begins by fogging of hypertonic saline, and ends with the nasal and oral suction of the patient. The evaluation of clinical data is done 10 minutes before, 10 minutes later, 2 hours after physiotherapy treatment. The evaluation will be do it for a doctor who will, in all patients, a clinical examination that includes all items scale clinical severity of acute bronchiolitis. Patient Registries: SELECTION OF THE POPULATION Reference population. Patients diagnosed acute viral bronchiolitis during the conduct of the trial and have been admitted to the University Hospital Virgin of Arrixaca. Sample size The sample calculation was done considering a reduction of 2 points after physiotherapy in bronchiolitis severity scale. Whereas: Variances: sames Detect mean difference: 2,000 Common standard deviation: 2,370 Ratio of sample sizes: 1,00 Confidence level: 95,0% The standard deviation values were obtained from: JM Fernández Ramos et al Validation of a clinical scale of severity of acute bronchiolitis. An Pediatr (Barc). 2014; 81 (1): 3-8, article in which the mean and standard deviation (SD) score of patients admitted was 7 ± 2.37. There are no items to compare this scale before and after treatment, so the investigators have assumed that value of common standard deviation (SD) and whereas a decrease of 2 points on the scale post-physical therapy would be clinically relevant. Power (%) Sample size Cases Control Total 85,0 27 27 54 90 31 31 62 Finally it was decided to increase to 60 cases / group considering that the number of losses may be higher (the investigators calculate 50%).

Interventions

OTHERNebulization of hypertonic saline

application of hypertonic saline serum through a mask fogging or a box fogging

OTHERProlonged slow expiration technique (PSE)

Passive expiratory aid implemented baby. the child is placed supine on a hard surface. Thoracoabdominal slow manual pressure that begins at the end of a spontaneous and continuous exhalation to residual volume is exercised. Oppose reaches 2 or 3 breaths. Vibrations can accompany the art. The goal is to achieve a greater expiratory volume.

OTHERPatient coughing Provocation (TP)

Tp is based on the mechanism reflects cough induced by stimulation of the buttons on the wall of the trachea extrathoracic mechanoreceptors. The child is placed supine. A short pressure is done with the thumb on the tracheal conduit (in the sternal notch) at the end of inspiration, or at the beginning of expiration. With the other hand holding the abdominal region we prevent the dissipation of energy and make the explosion tussive more effective. It is done after the PSE.

OTHERinspiratory maneuver to rhinopharyngeal cleaning DRR

After the inspiratory reflection following the PSE, the TP or crying. At the end of expiratory time the child's mouth is closed with the back of his hand just finished his chest support, raising the jaw and forcing the child to an inspiration with the nose

OTHERAspiration of secretions

Suctioning with a probe by a vacuum system installed on the wall.

Sponsors

Universidad Católica San Antonio de Murcia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
1 Months to 2 Years
Healthy volunteers
No

Inclusion criteria

* Patients admitted to the pediatric intensive care unit or pediatric nursing unit. Which they are diagnostic of acute viral bronchiolitis (AVB).

Exclusion criteria

* Presence of cyanotic congenital heart disease no longer for comparing the constants. * Relative or absolute contraindication CPT techniques included in the protocol. * Patients diagnosed with moderate or severe gastroesophageal reflux since the PSE gastroesophageal reflux can accentuate a previously exist. * Patients with laryngeal diseases caused because the cough is a technique that is applied directly to the tracheal wall and can affect the larynx. * Absence of cough reflects and presence of laryngeal stridor is a contraindication to chest physiotherapy in general. * Systematic presence of gag reflex as the aspiration of secretions and coughing caused nasobucales stimulate this reflex

Design outcomes

Primary

MeasureTime frame
Evaluate the effectiveness of a physiotherapy treatment with clinical severity scale of a patient diagnosed with acute viral bronchiolitisParticipants will be followed for the duration of hospital stay, an expected average of 7 days

Secondary

MeasureTime frameDescription
Assess the variation of score, a scale of severity of acute viral bronchiolitis, after intervention protocolsParticipants will be followed for the duration of hospital stay, an expected average of 7 days
Analyze a inquiry of subjective opinion, completed by parents or tutors at the end of treatmentParticipants will be followed for the duration of hospital stay, an expected average of 7 daysA questionnaire was filled out by parents or guardians of patients. After, the results of the survey will be analyzed by means of SPSS software
To quantify the changes in clinical score severity scale.Participants will be followed for the duration of hospital stay, an expected average of 7 days

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026