Hemodynamic Effects of Physiotherapy in the Early Postoperative Period
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT03726541 |
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Recruitment Status :
Completed
First Posted : October 31, 2018
Last Update Posted : March 7, 2019
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Physiotherapy Postoperative Lung Diseases | Other: physiotherapy | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 72 participants |
| Allocation: | N/A |
| Intervention Model: | Single Group Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Screening |
| Official Title: | Hemodynamic Effects of Physiotherapy in the Early Postoperative Period |
| Actual Study Start Date : | November 1, 2018 |
| Actual Primary Completion Date : | December 30, 2018 |
| Actual Study Completion Date : | December 30, 2018 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Early physiotherapy group
breathing exercise incentive spirometry training ambulation coughing
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Other: 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. |
- Change from baseline oxygen saturation [ Time Frame: 30 minutes ]The hearth rate response will be measured before and after exercise training with pulse oximeter.
- Change from baseline hearth rate response. [ Time Frame: 30 minutes ]The hearth rate response will be measured before and after exercise training with intensive care ECG
- Change from baseline systolic and diastolic blood pressure response. [ Time Frame: 30 minutes ]Blood pressure will be measured before and after exercise training with monometer from the arm
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| Ages Eligible for Study: | 18 Years to 75 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
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
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03726541
| Turkey | |
| Yedikule Chest Disease Hospital | |
| Istanbul, Zeytinburnu, Turkey, 34200 | |
| Study Chair: | Arif Balcı | Saglik Bilimleri Universitesi |
| Responsible Party: | esra pehlivan, Principal investigator, Istanbul Medipol University Hospital |
| ClinicalTrials.gov Identifier: | NCT03726541 |
| Other Study ID Numbers: |
Hemodynamics_ physiotherapy |
| First Posted: | October 31, 2018 Key Record Dates |
| Last Update Posted: | March 7, 2019 |
| Last Verified: | March 2019 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | Undecided |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Lung Diseases Respiratory Tract Diseases |

