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

Sponsor
Universidad Católica San Antonio de Murcia (Other)
Overall Status
Completed
CT.gov ID
NCT02458300
Collaborator
(none)
77
2
1.9

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Nebulization of hypertonic saline
  • Other: Prolonged slow expiration technique (PSE)
  • Other: Patient coughing Provocation (TP)
  • Other: inspiratory maneuver to rhinopharyngeal cleaning DRR
  • Other: Aspiration of secretions
N/A

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%).

Study Design

Study Type:
Interventional
Actual Enrollment :
77 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
FIBARRIX "Clinical Evaluation of the Response to Chest Physiotherapy in Infants With Acute Bronchiolitis"
Study Start Date :
Jan 1, 2015
Actual Primary Completion Date :
Mar 1, 2015
Actual Study Completion Date :
Mar 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Control Arm

Nebulized hypertonic saline. Aspiration of secretions

Other: Nebulization of hypertonic saline
application of hypertonic saline serum through a mask fogging or a box fogging

Other: Aspiration of secretions
Suctioning with a probe by a vacuum system installed on the wall.

Active Comparator: Intervention Arm.

Nebulization of hypertonic saline. Application of Prolonged slow expiration technique (PSE) expiratory volume. Patient coughing Provocation (TP) Inspiratory maneuver to rhinopharyngeal cleaning DRR Aspiration of secretions

Other: Nebulization of hypertonic saline
application of hypertonic saline serum through a mask fogging or a box fogging

Other: Prolonged 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.

Other: Patient 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.

Other: inspiratory 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

Other: Aspiration of secretions
Suctioning with a probe by a vacuum system installed on the wall.

Outcome Measures

Primary Outcome Measures

  1. Evaluate the effectiveness of a physiotherapy treatment with clinical severity scale of a patient diagnosed with acute viral bronchiolitis [Participants will be followed for the duration of hospital stay, an expected average of 7 days]

Secondary Outcome Measures

  1. Assess the variation of score, a scale of severity of acute viral bronchiolitis, after intervention protocols [Participants will be followed for the duration of hospital stay, an expected average of 7 days]

  2. Analyze a inquiry of subjective opinion, completed by parents or tutors at the end of treatment [Participants will be followed for the duration of hospital stay, an expected average of 7 days]

    A questionnaire was filled out by parents or guardians of patients. After, the results of the survey will be analyzed by means of SPSS software

  3. 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]

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Month to 2 Years
Sexes Eligible for Study:
All
Accepts 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

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Universidad Católica San Antonio de Murcia

Investigators

  • Principal Investigator: Enrique E Conesa Segura, PT, MurciaSalud
  • Principal Investigator: Susana Beatriz S Reyes Dominguez, PhD,MD, MurciaSalud
  • Study Chair: José J Rios Diaz, PhD, BiolSc, PT, Universidad Católica San Antonio de Murcia
  • Study Chair: Eduardo E Ramos Elbal, MD, MurciaSalud
  • Study Chair: Cristina C Palazón Carpe, MD, MurciaSalud
  • Study Chair: Maria Ángeles M Ruiz Pacheco, MD, MurciaSalud
  • Study Chair: Jaume J Enjuanes Llovet, MD, MurciaSalud
  • Study Chair: Sara S Francés Tarazona, MD, MurciaSalud
  • Study Chair: Sebastián S Gil Garcia, PT, MurciaSalud
  • Study Chair: Maía de los Ángeles M Martinez-Salazar Arboleas, PT, MurciaSalud

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Enrique Conesa Segura, PT, Universidad Católica San Antonio de Murcia
ClinicalTrials.gov Identifier:
NCT02458300
Other Study ID Numbers:
  • FIBARRIX
First Posted:
Jun 1, 2015
Last Update Posted:
Mar 2, 2016
Last Verified:
May 1, 2015
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Keywords provided by Enrique Conesa Segura, PT, Universidad Católica San Antonio de Murcia
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 2, 2016