Expiratory Muscle Training Versus Incentive Spirometry After Colorectal Surgery

NCT ID: NCT05290480

Last Updated: 2022-03-22

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

24 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-01-01

Study Completion Date

2019-04-10

Brief Summary

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The aim of this study was to compare the effects of expiratory muscle training (EMT) and incentive spirometry (IS) in addition to conventional pulmonary rehabilitation after colorectal surgery. Twenty-four individuals (13 male) undergoing colorectal surgery were included. They were randomly divided into two groups. In addition to conventional chest physiotherapy, group 1 was performed EMT (n=12), group 2 was performed deep breathing exercises with incentive spirometry (IS) in postoperative period. Respiratory muscle strength, functional capacity, levels of movement and independence, and postoperative pulmonary complications (PPC) were evaluated. Length of stay in hospital (LOS) was recorded.

Detailed Description

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The aim of this study was to compare the effects of expiratory muscle training (EMT) and incentive spirometry (IS) in addition to conventional pulmonary rehabilitation after colorectal surgery. Twenty-four individuals (13 male) undergoing colorectal surgery were included. They were randomly divided into two groups. In addition to conventional chest physiotherapy, group 1 was performed EMT (n=12), group 2 was performed deep breathing exercises with incentive spirometry (IS) in postoperative period. Respiratory muscle strength, functional capacity, levels of movement and independence, and postoperative pulmonary complications (PPC) were evaluated. Length of stay in hospital (LOS) was recorded

Conditions

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Colorectal Cancer Pulmonary Rehabilitation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Investigators
Treatment and evaluation were performed by two different physiotherapists. The assessing physiotherapist was blind to group allocation.

Study Groups

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Expiratory muscle training

participant performed expiratory muscle training with threshold device

Group Type EXPERIMENTAL

expiratory muscle training

Intervention Type OTHER

participants performed expiratory muscle training according to their maximum expiratory pressure that measured earlier in addition to conventional chest physiotherapy

Insentive spirometry

participant performed deep breathing exercise with insentive spirometry device

Group Type EXPERIMENTAL

Insentive spirometry

Intervention Type DEVICE

participants performed deep breating exercise with insentive spirometry in additional to convantional chest physiotherapy

Interventions

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expiratory muscle training

participants performed expiratory muscle training according to their maximum expiratory pressure that measured earlier in addition to conventional chest physiotherapy

Intervention Type OTHER

Insentive spirometry

participants performed deep breating exercise with insentive spirometry in additional to convantional chest physiotherapy

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* hemodynamically stable
* able to walk independently
* able to walk independently

Exclusion Criteria

* any contraindication for chest physiotherapy (unstable cardiovascular disease, severe pulmonary hypertension, corrected severe hypoxemia, exercise desaturation, rib fractures, subcutaneous emphysema, advanced osteoporosis, thrombocytopenia, effort dyspnea and vertigo)
* any metastases
* severe chronic cardiovascular disease
* candidates for organ transplantation
* abdominal hernia repair
* history of surgery more than one year
* orthopaedic or neurological disease that would prevent independent walking
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Pamukkale University

OTHER

Sponsor Role lead

Responsible Party

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Erhan KIZMAZ

research assistant

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Erhan KIZMAZ, Msc

Role: PRINCIPAL_INVESTIGATOR

Pamukkale University

Locations

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Pamukkale University

Denizli, Pamukkale, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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ekizmaz

Identifier Type: -

Identifier Source: org_study_id

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