Effects of the Breath Stacking Technique After Upper Abdominal Surgery

NCT ID: NCT04418700

Last Updated: 2021-04-26

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

32 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-06-01

Study Completion Date

2021-03-31

Brief Summary

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This study evaluates the effects of the breath stacking technique in patients after upper abdominal surgery. Half of the patients receive routine physical therapy associated with the Breath Stacking technique, while the other half will receive only routine physical therapy.

Detailed Description

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This randomized controlled study aims to evaluate the effects of the Breath Stacking technique in patients undergoing upper abdominal surgery on clinical, physiological and cardiopulmonary variables. These individuals were randomized to compose the control group (CG) and the intervention group (GBS). The routine physical therapy was performed in both groups and in the GBS two daily sessions of up to 20 minutes of Breath Stacking technique were applied. To verify the effect of this intervention, before and after the protocol, patients underwent the following evaluations: algometry, cirtometry in the axillary line , umbilical line and the xiphoid process, ventilometry, spirometry and manovacuometry.

Conditions

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Abdominal Surgery

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Breath Stacking technique

The intervention group will receive routine physical therapy associated with the Breath Stacking technique in 2 daily sessions of up to 20 minutes.

The technique consists of an Instrument composed of a one-way valve coupled to a face mask to promote the accumulation of successive inspiratory volumes.

Group Type EXPERIMENTAL

Breath Stacking

Intervention Type DEVICE

The patients will perform the maneuver through successive inspiratory efforts for 20 s. Subsequently, the expiratory branch will be unobstructed to allow expiration. This maneuver will be repeated 5 times in each series, with intervals of 30 seconds between them. The technique will be performed with the trunk inclined 30º in relation to the horizontal plane, in 3 series, with interval of 2 min completing 15 min of therapy.

Routine physical therapy

The control group will receive only routine physical therapy. Routine physiotherapy consists of breathing exercises, using techniques bronchial hygiene and pulmonary reexpansion, and motor physiotherapy through exercise passive, active-assisted or active mobilization, stretching, training activities of daily living, positioning and removal of the bed and guidelines for post-discharge.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Breath Stacking

The patients will perform the maneuver through successive inspiratory efforts for 20 s. Subsequently, the expiratory branch will be unobstructed to allow expiration. This maneuver will be repeated 5 times in each series, with intervals of 30 seconds between them. The technique will be performed with the trunk inclined 30º in relation to the horizontal plane, in 3 series, with interval of 2 min completing 15 min of therapy.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Patients undergoing a surgical procedure that involves in an incision in the upper quadrants of the abdominal region.

Exclusion Criteria

* Intolerance to the use of BS mask.
* Chronic obstructive pulmonary disease (COPD), Asthma, Chron's disease.
* Liver trauma severe with hemodynamic repercussions.
* Patients undergoing esophagectomy.
* Sepsis with complications postoperative hemodynamics.
* Need for surgical reintervention.
* Forwarded to Intensive Care Unit or need for mechanical ventilation after discharge from the anesthetic recovery.
* Cognitive dysfunction that makes it impossible to understand and execute evaluations and intervention.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Universidade Federal de Santa Maria

OTHER

Sponsor Role lead

Responsible Party

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Prof. Dr. Antônio Marcos Vargas da Silva

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Federal University of Santa Maria

Santa Maria, Rio Grande do Sul, Brazil

Site Status

Countries

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Brazil

References

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Fernandes DDL, Righi NC, Rubin Neto LJ, Belle JM, Pippi CM, Ribas CZDM, Nichele LFI, Signori LU, Silva AMVD. Effects of the breath stacking technique after upper abdominal surgery: a randomized clinical trial. J Bras Pneumol. 2022 Mar 14;48(1):e20210280. doi: 10.36416/1806-3756/e20210280. eCollection 2022.

Reference Type DERIVED
PMID: 35293484 (View on PubMed)

Other Identifiers

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11041019.0.0000.5346

Identifier Type: -

Identifier Source: org_study_id

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