Effect of Chest Physiotherapy on the Development of Preterm Infants.

NCT ID: NCT04689386

Last Updated: 2025-03-27

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

COMPLETED

Clinical Phase

NA

Total Enrollment

51 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-02-26

Study Completion Date

2024-12-31

Brief Summary

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The aim of this study is to investigate the effect of the stimulation of "reflex rolling" from the Vojta method and the effect of the expiratory flow increase technique on the development of the preterm infants. In the same way, it will be assessed whether the application of these techniques produce pain.

This application will be carried out in preterm infants of less than 32 weeks of gestation with neonatal respiratory distress syndrome (SDR) and carriers of mechanical ventilation. The intervention will take place in the neonatal intensive care unit (NICU) The intervention period is one month (4 weeks) and different follow-ups will be carried out at term age, at 3, 6, 9 and 12 months of corrected age.

Detailed Description

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Conditions

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Development, Infant Respiratory Distress Syndrome in Premature Infant

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Group I Stimulation of "reflex rolling" from the Vojta method

Group Type EXPERIMENTAL

Group I (GE-I) - Stimulation of "reflex rolling" from the Vojta method

Intervention Type OTHER

This manoeuvre does not require the newborn to be moved, but only a slight rotation of the head towards the side from which the stimulus is delivered. The starting position for performing the first phase of reflex rolling is the asymmetric supine position, with the limbs freely lying on the resting surface.

A digital pressure will exert on the chest area, where the mammillary line crosses the insertion of the diaphragm, either at the level of the 6th rib, or between the 5th and the 6th, or between the 6th and the 7th. A one minute stimulus will be performed on each side. The intervention will be repeated twice a day, ensuring that the period between one intervention and another is at least two hours.

Group II Expiratory flow increase technique

Group Type EXPERIMENTAL

Group II (GE-II) - expiratory flow increase technique

Intervention Type OTHER

The technique adapted to the premature infant will be performed. This maneuver consists of slowly applying light pressure to the infant's chest with one hand, obliquely, starting from the end of the inspiratory plateau until the end of expiration, which is prolonged. The hand should be placed between the sternal notch and the xiphoid process of the newborn's sternum. The therapist's other hand is placed on the last ribs (without applying pressure) as a bridge, of which the columns are the thumb and forefinger (or middle finger). Therefore, contact with the infant's abdomen is avoided and the expansion of the lower rib is limited, allowing a better displacement of the diaphragm and avoiding an increase in intra-abdominal pressure. The maneuver will be repeated three times, respecting the infant's responses and their physiological constants. The intervention will be repeated twice a day, trying to ensure that the period between one intervention and another is at least 2 hours.

Control Group

Routine intervention in the NICU with mechanical ventilation.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Group I (GE-I) - Stimulation of "reflex rolling" from the Vojta method

This manoeuvre does not require the newborn to be moved, but only a slight rotation of the head towards the side from which the stimulus is delivered. The starting position for performing the first phase of reflex rolling is the asymmetric supine position, with the limbs freely lying on the resting surface.

A digital pressure will exert on the chest area, where the mammillary line crosses the insertion of the diaphragm, either at the level of the 6th rib, or between the 5th and the 6th, or between the 6th and the 7th. A one minute stimulus will be performed on each side. The intervention will be repeated twice a day, ensuring that the period between one intervention and another is at least two hours.

Intervention Type OTHER

Group II (GE-II) - expiratory flow increase technique

The technique adapted to the premature infant will be performed. This maneuver consists of slowly applying light pressure to the infant's chest with one hand, obliquely, starting from the end of the inspiratory plateau until the end of expiration, which is prolonged. The hand should be placed between the sternal notch and the xiphoid process of the newborn's sternum. The therapist's other hand is placed on the last ribs (without applying pressure) as a bridge, of which the columns are the thumb and forefinger (or middle finger). Therefore, contact with the infant's abdomen is avoided and the expansion of the lower rib is limited, allowing a better displacement of the diaphragm and avoiding an increase in intra-abdominal pressure. The maneuver will be repeated three times, respecting the infant's responses and their physiological constants. The intervention will be repeated twice a day, trying to ensure that the period between one intervention and another is at least 2 hours.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Preterm Infants \<32 gestational age
* Admitted to the NICU
* With SDR
* Hemodynamically stable
* Stable convulsive pictures
* Controlled thermoregulation
* Mechanical ventilation (invasive or non-invasive)
* Parents / guardians of legal age, with sufficient cognitive ability to understand consent
* Signature of consent

Exclusion Criteria

* Periventricular leukomalacia
* Grade III and IV intraventricular hemorrhage
* Rib fracture
* Asphyxia at birth
* Necrotizing enterocolitis \> or = II B

Abandoned Criteria:

* Appearance of any of the complications mentioned above
* Hospital transfer
* Hospital discharge (if the intervention at home cannot be followed)
* Voluntary decision of parents / guardians to abandon the study
* Medical decision
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Fundación para la Salud Infantil de la Comunidad Valenciana

UNKNOWN

Sponsor Role collaborator

Universidad de Murcia

OTHER

Sponsor Role lead

Responsible Party

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Ana Igual Blasco

Degree in Physiotherapy

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Hospital General Universitario de Elche

Elche, Alicante, Spain

Site Status

Hospital Universitario Torrecárdenas

Almería, Almería, Spain

Site Status

Hospital Clínico Universitario Virgen de la Arrixaca

El Palmar, Murcia, Spain

Site Status

Countries

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Spain

References

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Other Identifiers

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74244433

Identifier Type: -

Identifier Source: org_study_id

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