Hemodynamic Effects of Physiotherapy in the Early Postoperative Period

NCT ID: NCT03726541

Last Updated: 2019-03-07

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

72 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-11-01

Study Completion Date

2018-12-30

Brief Summary

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Physiotherapy will be applied to the patients who undergo thoracotomy operation after 24 hours of intensive care stay. Physiotherapy program includes breathing exercises, incentive spirometer training, ambulation. Oxygen saturation, heart rate and blood pressure values will be recorded before and after the training session. Changes in the follow-up parameters will be discussed.

Detailed Description

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Conditions

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Physiotherapy Postoperative Lung Diseases

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

SCREENING

Blinding Strategy

NONE

Study Groups

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Early physiotherapy group

breathing exercise incentive spirometry training ambulation coughing

Group Type EXPERIMENTAL

physiotherapy

Intervention Type OTHER

Physiotherapy program includes breathing exercises, incisive spirometer study, grade ambulation. Oxygen saturation, heart rate and blood pressure values will be recorded before and after the session. Changes in the follow-up parameters will be discussed.

Interventions

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physiotherapy

Physiotherapy program includes breathing exercises, incisive spirometer study, grade ambulation. Oxygen saturation, heart rate and blood pressure values will be recorded before and after the session. Changes in the follow-up parameters will be discussed.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Between 18-75 age
* Hemodynamically stable
* Being conscious

Exclusion Criteria

* Excessive pain
* Neurological complications
* Posttraumatic and musculoskeletal problems to prevent exercise
* Do not want to be included in the study
* Fever above 38 degrees
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Istanbul Medipol University Hospital

OTHER

Sponsor Role lead

Responsible Party

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esra pehlivan

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Arif Balcı

Role: STUDY_CHAIR

Saglik Bilimleri Universitesi

Locations

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Yedikule Chest Disease Hospital

Istanbul, Zeytinburnu, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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Hemodynamics_ physiotherapy

Identifier Type: -

Identifier Source: org_study_id

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