- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT02437552
Cycle Ergometer Exercise in Phase I of Cardiac Rehabilitation After Cardiac Surgery
28. Januar 2021 aktualisiert von: Ada Clarice Gastaldi, University of Sao Paulo
The prevalence of heart diseases has increased significantly in recent years and it is a health public problem due to an increased risk of death by several reasons.
A cardiac surgery is an alternative of treatment for critical injuries heart valves and coronaries arteries.
Changes in respiratory system resulting from cardiac surgery are well established and include a reduced functional capacity due post-surgical pain, causing increased respiratory function and increased oxygen consumption .
The exercises with the cycle ergometer in phase I of cardiac rehabilitation can improve peripheral muscle strength, functional capacity and perception of dyspnea when used postoperatively and there are speculations if an earlier carried out can contribute to a better postoperative evolution of patients, but these benefits in phase I of the Rehabilitation Cardiac are not well defined in the literature.
Objective: To evaluate the exercises effects with ergometer cycle in the postoperative course of patients undergoing cardiac surgery.
Method: Patients will be recruited the cardiac surgery service of Polyclinic Pato Branco in the city of Pato Branco in state of Paraná, of both sexes, appropriate for the inclusion criteria, which will be evaluated by pulmonary function tests (strength of respiratory muscles, submaximal exercise test, dyspnea scales, laboratories tests and radiological exam).
All patients will be randomly assigned for one of two groups: the control group (Conventional treatment) and rehabilitation group (conventional treatment +cycle ergometer), for about 7 days at postoperative period.
Patients will be reevaluated on the third postoperative day and at discharge.
Clinical evolution data will be collected from the records and notes of the medical staff and monitoring physiotherapist.
Studienübersicht
Status
Zurückgezogen
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
The research will be a randomized controlled clinical trial.
The study will be conducted at the Polyclinic Pato Branco, in the city of Pato Branco Parana - Brazil and this study already approved by the Ethics Committee Clinical Hospital and Faculty of Medicine, University of São Paulo and all participants sign the consent form informed.
For the implementation of research wil be recruited patients heart surgery who fit the inclusion criteria and do not show any characteristics of the exclusion criteria, which agree to participate and sign the consent form free and informed.
The equipment and tests are already included in routine admissions of patients, approved by the hospital and the Brazilian Public Health System (SUS).
Studientyp
Interventionell
Phase
- Unzutreffend
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienorte
-
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Paraná
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Pato Branco, Paraná, Brasilien, 85501250
- Policlínica Pato Branco
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Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
30 Jahre bis 70 Jahre (Erwachsene, Älterer Erwachsener)
Akzeptiert gesunde Freiwillige
Nein
Studienberechtigte Geschlechter
Alle
Beschreibung
Inclusion Criteria:
- Patients undergoing cardiac surgery type Myocardial Revascularization and Exchange Mitral Valve Aortic, both sexes and aged between 30-75 years.
Exclusion Criteria:
Patients undergoing surgical correction of heart disease congenital, aortic aneurysm and dissection of aorta;
- Present disabling disease to accomplish what is proposed in study as previous stroke, mental or motor deficit, hearing loss, amputation of the lower limbs (unilateral or bilateral);
- Present psychomotor agitation of immediate postoperative and first postoperative and history weaning failure in the immediate;
- Instability hemodynamics and vasoactive drugs;
- Present what other type of peri and postoperative complications;
- Re-operation within 24 hrs.
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Single
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
---|---|
Placebo-Komparator: Control group: routine physiotherapy
Are patients who carry out the routine already established the Unit, consisting of the first post surgery, the patient lying down doing the breathing exercises, active exercises ends and active-assisted upper (UL) and lower limbs (LL),
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routine physiotherapy
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Aktiver Komparator: Intervention group: ergometer cycle exercise
Are the patients who will carry out the exercises routine over the cycle ergometer twice daily from 3 PO for 5 minutes with its progressiveness at discharge for ward for 10 minutes
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routine physiotherapy
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
Change of six-minute walk test (6MMWT) distance
Zeitfenster: Before surgery ,third and seventh postoperative day
|
The six-minute walk test will be conducted with monitoring blood pressure, HR, RR and SpO2 in a hall plan, with distances previously marked.
The patient will be accompanied by the researcher and encouraged by constant verbal stimulation, walking as fast as possible, if the patient stop walking the timer will keep triggered.
Will use the oximeter with the sensor on the third finger of the right hand, and a certain reading after the signal stabilization and at the same time we get the heart rate.
Will be used to calculate the expected value, and reference to distance in the 6MWT, the equations proposed by Enright and Sherrill (1998) determining the percentage of predicted for each test performed by patient.
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Before surgery ,third and seventh postoperative day
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
Change of spirometric values
Zeitfenster: Before surgery ,third and seventh postoperative day
|
Spirometry will be performed according to criteria of the American Thoracic Society and the Brazilian Consensus Spirometry.
Values will be observed from CVF, VEF1 e PEF.
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Before surgery ,third and seventh postoperative day
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Andere Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
Change of respiratory muscle strength - Mouth pressure measurements
Zeitfenster: Before surgery ,third and seventh postoperative day
|
Manovacuometry will be performed with the patient seated with nasal clip, the display scale with intervals of 4 cmH2O and variation +/- 120 cmH2O.
The highest value obtained during the two maneuvers will be compared to the table described by Neder et al (1999), which predicts expected values for the Brazilian population according to gender and age.
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Before surgery ,third and seventh postoperative day
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Change of perceived dyspnea
Zeitfenster: Before surgery ,third and seventh postoperative day
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The perceived effort is used the Borg Scale modified scored from 0 to 10.
And dyspnea scale will be scored from 0 to 4 according to the intensity of dyspnea and is based on used the scale of the Medical Research Council (MRC).
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Before surgery ,third and seventh postoperative day
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Change of body mass index
Zeitfenster: Before surgery and postoperative seventh day
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The BMI will be calculated using the classical formula: BMI = current weight (kg) / A2 (m).
The following lower limits of normal were considered: BMI <21 for age group 35-44 years; <22 for 45-54 years; <23 for 55 -64 years and <24 to 65 above years.
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Before surgery and postoperative seventh day
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Change of cirtometry
Zeitfenster: Before surgery ,third and seventh posoperative day
|
Cirtometry will be held in myocardial revascularization of patients who use the saphenous and waist hip will be performed in all patients.
Will be used a tape measure.
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Before surgery ,third and seventh posoperative day
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Change of peripheral muscle strength
Zeitfenster: Before surgery ,third and seventh postoperative day
|
The peripheral muscle strength assessment test will be the end of the test the foot, the patient will be instructed to stay barefoot with his right hand resting on the front wall and with a semi elbow flexion to aid maintenance balance.
Prior to testing, the participant will be oriented make a plantar flexion to the point of support of the joints metatarsophalangeal and this time will be marked by the examiner through a mark on the wall and the patient will be informed that should reach the one marked point.
The test itself consisted of time, in seconds, the time it takes to perform five push-ups as plantar soon as possible.
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Before surgery ,third and seventh postoperative day
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Change in cortisol levels
Zeitfenster: Before surgery ,third and seventh postoperative day
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Laboratory evaluation will be performed by laboratory staff of hospital with a blood sample from the patient, which will be assessed the cortisol levels .
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Before surgery ,third and seventh postoperative day
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change of radiological assessment
Zeitfenster: Before surgery ,third and seventh postoperative day
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Radiological assessment will be held the day before the surgery, the third post-operative and post-operative seventh, the clinic Radiology Southwest - Pato Branco - Paraná to assess complications lung from surgery.
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Before surgery ,third and seventh postoperative day
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Adherence evaluation
Zeitfenster: Third and seventh postoperative day
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The questionnaire will be administered at the end of the first contact of the patient the exercises with the cycle ergometer to assess adherence running a differential exercise during your surgical recovery.
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Third and seventh postoperative day
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Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
Publikationen und hilfreiche Links
Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Primärer Abschluss (Tatsächlich)
28. Januar 2021
Studienanmeldedaten
Zuerst eingereicht
29. April 2015
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
6. Mai 2015
Zuerst gepostet (Schätzen)
7. Mai 2015
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
2. Februar 2021
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
28. Januar 2021
Zuletzt verifiziert
1. Januar 2021
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Andere Studien-ID-Nummern
- USP 2015-1
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
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