Physical Activity in Renal Disease (PAIRED): The Effect on Hypertension
Chronic Kidney Diseases
About this trial
This is an interventional treatment trial for Chronic Kidney Diseases
Eligibility Criteria
Inclusion Criteria:
- Resting SBP >120 mmHg systolic on screening BP clinic measurements (with an electronic sphygmomanometer, mean of three readings after first reading is discarded) and at least one previous SBP measurement above 120 mmHg on a separate occasion within the past six months (home or clinic measurement).
- Stable on blood pressure medications for the past eight weeks
- eGFR 15-44 ml/min per 1.73m2 eGFR between 15-44 ml/min per 1.73m2 within the last three months and one additional value in this rage in the last 12 months.
- Independent ambulation with or without an assistive device for at least three consecutive minutes
- Cognition and English language sufficient enough to understand written information, provide consent, and comply with the testing and interventions
- Approval of the attending nephrologist
- No significant exercise-induced arrhythmia or new ischemia on submaximal incremental exercise testing (final screening step)
Exclusion Criteria:
- Resting SBP >160 mmHg or DBP > 110 mmHg on screening BP clinic measurement (Note: the individual may be re-screened 8 weeks after medication adjustment)
- Arm circumference greater than 54 centimeters (size limit of large ABPM cuff)
- Recent (<6 weeks) or planned (<6 months) major cardiovascular events or procedures
- Any known contraindication to exercise (American College of Sports Medicine Guidelines)
Acute myocardial infarction (3-5 days) or unstable angina; Uncontrolled symptomatic arrhythmias; Active endocarditis; Acute myocarditis or pericarditis; Symptomatic severe aortic stenosis; Acute pulmonary embolism or deep vein thrombosis; Suspected dissecting aneurysm; Uncontrolled asthma; Uncontrolled pulmonary edema; Room air desaturation to <85%; Acute non-cardiopulmonary disorder that may affect exercise performance (infection, orthopedic problem); Mental impairment leading to inability to cooperate; Uncontrolled hypertension (as above)
- Pregnant or planning to become pregnant
- Transplant
- Life expectancy or predicted time to renal replacement therapy <9 months (attending physician judgment)
- Planned move or hospital admission within the next 9 months
- Currently enrolled in an interventional clinical trial; currently enrolled in a structured exercise program or performing regular exercise training > 2 day/week in the last 3 months
- Taking other medications known to affect blood pressure (prednisone cyclosporine) and expected adjustment in the next 9 months
- Significant barrier to participation in a home exercise program or an insurmountable barrier to attend in-center training sessions.
Sites / Locations
- Royal Alexandra Hospital
- University of Alberta Hospital, outpatient dialysis unit
- Grey Nuns Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Other
Exercise
Enhanced usual care
Personnel experienced in training people with chronic conditions (exercise specialist) will supervise the exercise training. At each in-center session in phase 1, the patient's exercise will be monitored to assess whether they are achieving target levels. Training intensities will be prescribed based on the most recent exercise test. Phase 1: an eight-week program of once weekly-supervised facility-based exercise sessions and twice weekly home-based sessions. Phase 2: a 16-week home-based exercise program overseen by an exercise specialist. During this phase, participants will be progressed through their home-based exercise program from Phase 1 on an individual basis. i. Frequency. A minimum of three exercise sessions per week. ii. Intensity. A moderate intensity (40-60% heart rate reserve) based on exercise testing. iii. Time. 150 minutes of exercise per week. iv. Type. We will prescribe aerobic exercise supplemented with isometric resistance exercises.
Participants in the control group will perform accelerometry. This is enhanced usual care because physical activity measurement is not routinely performed in CKD clinics. Control arm participants will only receive their accelerometry data after they have completed the study.