Coronary Artery Disease Clinical Trial
Official title:
The Effect of a Physiotherapy Prehabilitation Programme on Postoperative Outcomes in Patients Undergoing Cardiac or Thoracic Surgery
The purpose of this study is to determine the effects of a physiotherapy prehabilitation programme (walking and deep breathing exercises) in cardiac or thoracic patients by measuring changes in lung volumes, functional capacity physiotherapy length of stay postoperatively.
Preoperative rehabilitation or "Prehabilitation" can be defined as "the process of enhancing
the functional capacity of the individual to enable him or her to withstand a stressful
event". Prehabilitation is a relatively new concept with emerging evidence demonstrating a
reduction in length of hospital stay and disability, improved functional capacity and quality
of life as well as fewer peri-operative complications compared to usual care.
Patients who are awaiting Cardiothoracic surgery are often fearful of being physically
active, however extended periods of physical inactivity lead to a loss of muscle mass,
physical deconditioning and pulmonary complications which can in turn lead to decreased
quality of life, higher levels of morbidity, increased hospital length of stay and even
fatality.
Based on literature supporting the positive effects of physical activity, physiotherapy
prehabilitation aims to enhance functional exercise capacity in patients undergoing
Cardiothoracic surgery and hence minimising the risk of postoperative morbidity and enhancing
postsurgical recovery. Although there is evidence for prehabilitation in cardiothoracic
specialties these are mainly within heart failure patients therefore not comparable to
patients undergoing CABG or lobectomy surgeries.
The aim of this study is to determine whether a home based preoperative prehabilitation
programme improves patients' functional capacity, as measured by a 6 minute walk test (6MWT)
prior to surgery and improve post surgical recovery and recovery of functional capacity
earlier. This study will compare functional capacity levels from baseline (at time of being
accepted for surgery) and on the day of admission for surgery. Secondary aims are to
determine functional capacity prior to discharge from hospital and at 6-8 week follow up
appointment. Increasing maximal tidal volumes preoperatively would in turn decrease the
chance of atelectasis postoperatively thereby decreasing pulmonary complications. Time to
achieve discharge criteria from physiotherapy and total post-operative hospital length of
stay will be assessed. Patient health related satisfaction will be assessed using the EQ-5D.
The endpoint of this study will be when the patient returns for their routine 6-8 week follow
up appointment and completes final 6MWT, tidal volume (TV) measurement and EQ-5D.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT06030596 -
SPECT Myocardial Blood Flow Quantification for Diagnosis of Ischemic Heart Disease Determined by Fraction Flow Reserve
|
||
Completed |
NCT04080700 -
Korean Prospective Registry for Evaluating the Safety and Efficacy of Distal Radial Approach (KODRA)
|
||
Recruiting |
NCT03810599 -
Patient-reported Outcomes in the Bergen Early Cardiac Rehabilitation Study
|
N/A | |
Recruiting |
NCT06002932 -
Comparison of PROVISIONal 1-stent Strategy With DEB Versus Planned 2-stent Strategy in Coronary Bifurcation Lesions.
|
N/A | |
Not yet recruiting |
NCT06032572 -
Evaluation of the Safety and Effectiveness of the VRS100 System in PCI (ESSENCE)
|
N/A | |
Recruiting |
NCT04242134 -
Drug-coating Balloon Angioplasties for True Coronary Bifurcation Lesions
|
N/A | |
Recruiting |
NCT05308719 -
Nasal Oxygen Therapy After Cardiac Surgery
|
N/A | |
Completed |
NCT04556994 -
Phase 1 Cardiac Rehabilitation With and Without Lower Limb Paddling Effects in Post CABG Patients.
|
N/A | |
Recruiting |
NCT05846893 -
Drug-Coated Balloon vs. Drug-Eluting Stent for Clinical Outcomes in Patients With Large Coronary Artery Disease
|
N/A | |
Recruiting |
NCT06027788 -
CTSN Embolic Protection Trial
|
N/A | |
Recruiting |
NCT05023629 -
STunning After Balloon Occlusion
|
N/A | |
Completed |
NCT04941560 -
Assessing the Association Between Multi-dimension Facial Characteristics and Coronary Artery Diseases
|
||
Completed |
NCT04006288 -
Switching From DAPT to Dual Pathway Inhibition With Low-dose Rivaroxaban in Adjunct to Aspirin in Patients With Coronary Artery Disease
|
Phase 4 | |
Completed |
NCT01860274 -
Meshed Vein Graft Patency Trial - VEST
|
N/A | |
Recruiting |
NCT06174090 -
The Effect of Video Education on Pain, Anxiety and Knowledge Levels of Coronary Bypass Graft Surgery Patients
|
N/A | |
Terminated |
NCT03959072 -
Cardiac Cath Lab Staff Radiation Exposure
|
||
Completed |
NCT03968809 -
Role of Cardioflux in Predicting Coronary Artery Disease (CAD) Outcomes
|
||
Recruiting |
NCT05065073 -
Iso-Osmolar vs. Low-Osmolar Contrast Agents for Optical Coherence Tomography
|
Phase 4 | |
Recruiting |
NCT04566497 -
Assessment of Adverse Outcome in Asymptomatic Patients With Prior Coronary Revascularization Who Have a Systematic Stress Testing Strategy Or a Non-testing Strategy During Long-term Follow-up.
|
N/A | |
Completed |
NCT05096442 -
Compare the Safety and Efficacy of Genoss® DCB and SeQuent® Please NEO in Korean Patients With Coronary De Novo Lesions
|
N/A |