Effect of Early Bedside Cycling Exercises on Selected Physical and Psychological Outcomes in Patients After Heart Valve Surgery
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Cairo University
- Enrollment
- 41
- Locations
- 1
- Primary Endpoint
- Length of hospital stay
Study Overview
Brief Summary
The aim of this clinical trial is to assess the effect of early bedside cycling exercises post heart valve surgeries. the main question aims to answer: whether adding an early bedside cycling exercise will have an effect on patient's functional capacity, other physical outcomes and have an effect on patient's psychological state?
The participant will be assessed blindly the physical and psychological outcomes before getting randomly allocated in groups. the bedside cycling will be introduced and conducted in the intervention group in addition to the conventional physical therapy cardiac rehabilitation routine through preexisted physical therapy staff who present the hospital:
The routine use of breathing exercises, coughing techniques, chest wall vibrations, and mobilization is common during the first postoperative days.
On the other hand, the control group will only receive the conventional rehabilitation, subsequently, both groups will be assessed and compared by addressing the difference of the outcomes before discharging from the hospital.
Detailed Description
The aim of the study is to assess the effect of early bedside cycling exercises on selected physical and psychological outcomes in patients after heart valve surgery.
This study will be carried out on fifty patients diagnosed with valve heart disease and undergoing valve replacement or intervention. They will be recruited from National Heart Institute-Cairo, Egypt.
The purpose, nature and the risk of the study will be explained to the patients and each patient will be consented prior to participation in the study.
The patients in this study will randomly be assigned and randomly allocated into two equal groups (n=25), the intervention group will be treated daily from being extubated and being relatively stable until discharge from the hospital:
- Study group (25 patients): will receive bedside cycling in addition to the medical treatment and physiotherapy protocol.
- Control group (25 patients): will receive only routine physiotherapy treatment protocol and the medical treatment.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Double (Participant, Care Provider)
Masking Description
Patient are masked through out the study and health care providers who provide routine care of the patient whether are nurses, physicians or existed physiotherapist are also masked
Eligibility Criteria
- Ages
- 20 Years to 40 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Fifty patients with valvular heart disease (VHD)who have undergone valve surgical intervention
- •Their age between 20-40 years old.
- •Both genders
Exclusion Criteria
- •Cognitive impairment.
- •Neurological disorders.
- •Sever Musculoskeletal disorders (MSD) e.g. (late stages of osteoarthritis).
- •Underlying pulmonary diseases (aspiration pneumonia, chronic obstructive pulmonary disease, pneumothorax, etc).
- •Presence of comorbidities like:
- •Liver disease e.g. Active cirrhosis or history of previous liver transplant.
- •Renal disease e.g. Chronic renal disease, Renal failure.
- •Complicated operative course: post-operative complication:
- •a) Presence of preoperative cofounder complication: pulmonary hypertension (Pulmonary artery pressure) = which estimated by right ventricular systolic pressure (RVSP) is greater than 50 mmHg, left ventricular dysfunction which estimated left ventricular ejection fraction equals 40 % or less.
- •b) Patients with Coronary artery bypass surgery, active infective endocarditis, acute valve dysfunction and other acute urgent conditions.
Arms & Interventions
Bedside cycling Group
Participants (25 patients) that will receive bedside cycling:
- Intensity:
- RPE from 11 to 13 (scale 6-20)
- Resting HR + 20-30 bpm (up to tolerance if non-symptomatic), from low intensity and progressed to medium intensity.
- Duration: Session duration: Total duration of 20 min, early morning.
- Frequency: once daily from medically stable until discharge. in addition the medical treatment and routinely physiotherapy protocol.
Intervention: Bedside cycling (Device)
Routine physical therapy Group
participant that will receive only routine physiotherapy treatment protocol and the medical treatment.
Intervention: control (Other)
Outcomes
Primary Outcomes
Length of hospital stay
Time Frame: through study completion, an average of 2 weeks.
compare the intervention group to control group length of hospital stay.
Activities of Daily Living and Functional level
Time Frame: through study completion, an average 7 days
measuring Activities of Daily Living and Function level by using Barthel Index, the current level of 10 items the maximum score is 100, the lower scores ranging from 0- 20 indicating increased disability.
the Quality of Life
Time Frame: from the date of patient admission to the hospital until date of the surgical operation, an average of 2 weeks.
The Short Form-12 Health Questionnaire was used to measure the Quality of Life over the past 4 weeks, consisting of two components: physical and mental. The highest possible score for the mental component was 60.75781, indicating a better mental condition. Similarly, the highest possible score for the physical component was 56.577706, indicating a better physical condition.
Functional capacity
Time Frame: through study completion, an average of 2 weeks.
measured by Six Minutes Walk Test, it will be performed on a flat surface, with a predetermined distance 30 meters measured and marked off. Patients will be asked to walk self-paced back and forth between the 2 marked points for 6 minutes. Rests are allowed, and administrators are able to provide standardized feedback during and at the end of the test, The laps are counted, and a distance walked in 6 minutes is determined.
Forced Vital Capacity
Time Frame: through study completion, an average of 2 weeks.
measured by Spirometry Pulmonary function test, (THOR laboratory Spiro Tube PC Spirometer) will assess Forced Vital Capacity (FCV) in liters.
Psychological status
Time Frame: through study completion, an average of 2 weeks.
The Depression Anxiety Stress Scales 42 were used to measure three negative emotional states (depression, anxiety, and stress) experienced by the patients in the previous week. A higher score on the scale indicates a more severe condition, with the highest possible score being 126 and the lowest score being 0.
Forced Vital Capacity
Time Frame: from the date of patient admission to the hospital until date of the surgical operation, an average of 2 weeks.
measured by Spirometry Pulmonary function test, (THOR laboratory Spiro Tube PC Spirometer) will assess Forced Vital Capacity (FCV) in liters.
Functional capacity
Time Frame: from the date of patient admission to the hospital until date of the surgical operation, an average of 2 weeks.
measured by Six Minutes Walk Test, it will be performed on a flat surface, with a predetermined distance 30 meters measured and marked off. Patients will be asked to walk self-paced back and forth between the 2 marked points for 6 minutes. Rests are allowed, and administrators are able to provide standardized feedback during and at the end of the test, The laps are counted, and a distance walked in 6 minutes is determined.
Psychological status
Time Frame: from the date of patient admission to the hospital until date of the surgical operation, an average of 2 weeks.
The Depression Anxiety Stress Scales 42 were used to measure three negative emotional states (depression, anxiety, and stress) experienced by the patients in the previous week. A higher score on the scale indicates a more severe condition, with the highest possible score being 126 and the lowest score being 0.
Activities of Daily Living and Functional level
Time Frame: within the first 24-hour post-surgery
measuring Activities of Daily Living and Function level by using Barthel Index, the current level of 10 items the maximum score is 100, the lower scores ranging from 0- 20 indicating increased disability.
Secondary Outcomes
- Prothrombin International Normalized Ratio (INR)(1 month follow-up.)
- Functional Capacity(1 month follow-up.)
- Psychological status(1 month follow-up.)
- the Quality of Life(1 month follow-up.)
- Incidence of adverse event(from the date of beginning cycling intervention or routinely physiotherapy until the date of discharge and will be assessed up to one month.)
Investigators
Salwa Asem Abusarea Milegy
Teaching assistant in faculty of physical therapy Cairo university
Cairo University