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Physical Activity in Renal Disease (PAIRED): The Effect on Hypertension

Primary Purpose

Chronic Kidney Diseases

Status
Terminated
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
Exercise
Enhanced usual care
Sponsored by
University of Alberta
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Kidney Diseases

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Experimental

Other

Arm Label

Exercise

Enhanced usual care

Arm Description

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.

Outcomes

Primary Outcome Measures

24-hour ambulatory SBP
mean 24-hour ambulatory systolic blood pressure

Secondary Outcome Measures

antihypertensive use
Using the assigned DDD (WHO) for that drug
KDQOL-36
Kidney Disease and Quality of Life instrument - this is a short form that includes the SF-12 plus the burden of kidney disease, symptoms/problems of kidney disease, and effects of kidney disease scales from the KDQOL-SF
IPAQ-SF
International Physical Activity Questionnaire - Short Form
SEE scale
Self Efficacy for Exercise questionnaire - the total score ranges from 0 to 90. High scores indicate higher self-efficacy in exercise. There are 9 questions; responses vary from 0 to 10. The mean score on each question is 5.5.
EQ-5D
European Quality of Life (EuroQOL) health questionnaire with 5 dimensions
pulse wave velocity
measurement of aortic stiffness (femoral carotid, radial carotid)
body mass index
calculated as weight in kilograms divided by height in meters squared
Fat mass
Body composition using bioimpedance spectroscopy
clinic blood pressure
with a oscillometric sphygmomanometer
Oxygen uptake (VO2 peak)
Cardiopulmonary exercise testing
estimated glomerular filtration rate
c-reactive protein
total cholesterol
LDL
HDL
triglycerides
HgA1C
glycated hemoglobin
spot urinary sodium
measured on a non-exercise day
spot urinary protein
measured on a non-exercise day
7-day accelerometry
number of steps
7-day accelerometry
sedentary time
7-day accelerometry
time in light activity
7-day accelerometry
time in moderate activity
7-day accelerometry
time in vigorous activity
7-day accelerometry
time in very vigorous activity
7-day accelerometry
METS
7-day accelerometry
sedentary bouts
24-hour ABPM
daytime, night time systolic and diastolic BP
Adherence
70% of in centre sessions attended and 70% of home sessions performed prescribed (accelerometry and log book)
Body cell mass
Body composition using bioimpedance spectroscopy

Full Information

First Posted
May 12, 2018
Last Updated
April 28, 2021
Sponsor
University of Alberta
Collaborators
Canadian Institutes of Health Research (CIHR)
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1. Study Identification

Unique Protocol Identification Number
NCT03551119
Brief Title
Physical Activity in Renal Disease (PAIRED): The Effect on Hypertension
Official Title
Physical Activity in Renal Disease (PAIRED): A Randomized Controlled Trial of the Effect on Hypertension
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Terminated
Why Stopped
Covid-19 pandemic
Study Start Date
November 21, 2018 (Actual)
Primary Completion Date
August 13, 2020 (Actual)
Study Completion Date
August 20, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Alberta
Collaborators
Canadian Institutes of Health Research (CIHR)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Background and importance: Hypertension is highly prevalent among Canadians with non-dialysis dependent chronic kidney disease (CKD). It is a modifiable risk factor for both cardiovascular (CV) events and CKD progression. Exercise is an effective strategy for blood pressure (BP) reduction in the general population but in people with CKD, hypertension is mediated by different causes (i.e. vascular stiffness, volume expansion) and it is unclear whether exercise will reduce BP in this population. Consequently, exercise resources are not offered in the routine multidisciplinary care of people with CKD and the prevalence of sedentary behaviour remains double that of the general population. The role of exercise in CKD management is also an important question for patients. From CIHR-supported workshops with patients, the role of lifestyle, such as exercise in CKD was a top research priority. Research aims: i.To determine the effect of exercise on mean ambulatory systolic blood pressure (SBP) in people with CKD compared to usual care. The investigators hypothesize that exercise training will significantly reduce BP compared to control. ii.To inform the design of a larger, multi-center trial evaluating the effect of exercise on the risk of CKD progression. Methods: A 160 participant, single center randomized trial of adults from Alberta Kidney Care North CKD clinics, Edmonton, Albert, Canada. Participants with an estimated glomerular filtration rate (eGFR) of 15-44 ml/min per 1.73m2 and SBP >130 mmHg will be randomized, stratified by eGFR (<30 versus ≥ 30) to an exercise intervention or usual care. The main outcome is the difference in 24-hour ambulatory SBP after eight weeks of exercise training between groups. Secondary outcomes include: BPs at eight and 24 weeks, dose of anti-hypertensives, aortic stiffness, CV-risk markers, CV fitness, 7-day accelerometry, quality of life, safety, and in an exploratory analysis, eGFR and proteinuria. The intervention is thrice weekly moderate intensity aerobic exercise supplemented with isometric resistance exercise, targeting 150 minutes per week and delivered over 24-weeks. Phase 1: one supervised weekly sessions and home-based sessions (eight weeks). Phase 2: home-based sessions (16 weeks). To detect a clinically important BP reduction of 5 mmHg between groups requires 128 patients (two sample t-test, alpha 0.05, beta 0.2, common standard deviation of 10 mmHg). Assuming 20% dropout requires 160 patients. For the primary outcome, the investigators will use a mixed linear regression model in which BP is regressed on group, baseline SBP and eGFR, and time point. Expected outcomes: The findings from this study will address a significant knowledge gap in hypertension management in CKD, inform care-delivery and the design of a larger study on CKD progression. This proposal aligns with priorities for both patients and decision makers: to identify the role of exercise in CKD management and to reshape the delivery of renal care so that it is more consistent with patient values and preferences.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Diseases

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
In this parallel arm control trial, participants recruited from outpatient CKD clinics in Alberta Kidney Care North, Edmonton, Alberta, Canada will be randomized (1:1) to enhanced usual care (measurement of physical activity levels) or an exercise intervention.
Masking
Outcomes Assessor
Masking Description
Due to the nature of the intervention, participants cannot be blinded to group assignment; however, the primary outcome is objectively measured (24-hour ambulatory blood pressure measurement). For main trial secondary outcomes, assessors will be blinded to allocation status.
Allocation
Randomized
Enrollment
44 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Exercise
Arm Type
Experimental
Arm Description
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.
Arm Title
Enhanced usual care
Arm Type
Other
Arm Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Exercise
Intervention Description
See previous description
Intervention Type
Other
Intervention Name(s)
Enhanced usual care
Intervention Description
See previous description
Primary Outcome Measure Information:
Title
24-hour ambulatory SBP
Description
mean 24-hour ambulatory systolic blood pressure
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
antihypertensive use
Description
Using the assigned DDD (WHO) for that drug
Time Frame
8 and 24 weeks
Title
KDQOL-36
Description
Kidney Disease and Quality of Life instrument - this is a short form that includes the SF-12 plus the burden of kidney disease, symptoms/problems of kidney disease, and effects of kidney disease scales from the KDQOL-SF
Time Frame
8 and 24 weeks
Title
IPAQ-SF
Description
International Physical Activity Questionnaire - Short Form
Time Frame
8 and 24 weeks
Title
SEE scale
Description
Self Efficacy for Exercise questionnaire - the total score ranges from 0 to 90. High scores indicate higher self-efficacy in exercise. There are 9 questions; responses vary from 0 to 10. The mean score on each question is 5.5.
Time Frame
8 and 24 weeks
Title
EQ-5D
Description
European Quality of Life (EuroQOL) health questionnaire with 5 dimensions
Time Frame
8 and 24 weeks
Title
pulse wave velocity
Description
measurement of aortic stiffness (femoral carotid, radial carotid)
Time Frame
8 and 24 weeks
Title
body mass index
Description
calculated as weight in kilograms divided by height in meters squared
Time Frame
8 and 24 weeks
Title
Fat mass
Description
Body composition using bioimpedance spectroscopy
Time Frame
8 and 24 weeks
Title
clinic blood pressure
Description
with a oscillometric sphygmomanometer
Time Frame
8 and 24 weeks
Title
Oxygen uptake (VO2 peak)
Description
Cardiopulmonary exercise testing
Time Frame
8 and 24 weeks
Title
estimated glomerular filtration rate
Time Frame
8 and 24 weeks
Title
c-reactive protein
Time Frame
8 and 24 weeks
Title
total cholesterol
Time Frame
8 and 24 weeks
Title
LDL
Time Frame
8 and 24 weeks
Title
HDL
Time Frame
8 and 24 weeks
Title
triglycerides
Time Frame
8 and 24 weeks
Title
HgA1C
Description
glycated hemoglobin
Time Frame
24 weeks
Title
spot urinary sodium
Description
measured on a non-exercise day
Time Frame
8 and 24 weeks
Title
spot urinary protein
Description
measured on a non-exercise day
Time Frame
8 and 24 weeks
Title
7-day accelerometry
Description
number of steps
Time Frame
8 and 24 weeks
Title
7-day accelerometry
Description
sedentary time
Time Frame
8 and 24 weeks
Title
7-day accelerometry
Description
time in light activity
Time Frame
8 and 24 weeks
Title
7-day accelerometry
Description
time in moderate activity
Time Frame
8 and 24 weeks
Title
7-day accelerometry
Description
time in vigorous activity
Time Frame
8 and 24 weeks
Title
7-day accelerometry
Description
time in very vigorous activity
Time Frame
8 and 24 weeks
Title
7-day accelerometry
Description
METS
Time Frame
8 and 24 weeks
Title
7-day accelerometry
Description
sedentary bouts
Time Frame
8 and 24 weeks
Title
24-hour ABPM
Description
daytime, night time systolic and diastolic BP
Time Frame
8 and 24 weeks
Title
Adherence
Description
70% of in centre sessions attended and 70% of home sessions performed prescribed (accelerometry and log book)
Time Frame
8 and 24 weeks
Title
Body cell mass
Description
Body composition using bioimpedance spectroscopy
Time Frame
8 and 24 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stephanie Thompson, MD PhD
Organizational Affiliation
University of Alberta
Official's Role
Principal Investigator
Facility Information:
Facility Name
Royal Alexandra Hospital
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T5H 3V9
Country
Canada
Facility Name
University of Alberta Hospital, outpatient dialysis unit
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T6G 2P4
Country
Canada
Facility Name
Grey Nuns Hospital
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T6L5X8
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
30736832
Citation
Thompson S, Wiebe N, Gyenes G, Davies R, Radhakrishnan J, Graham M. Physical Activity In Renal Disease (PAIRED) and the effect on hypertension: study protocol for a randomized controlled trial. Trials. 2019 Feb 8;20(1):109. doi: 10.1186/s13063-019-3235-5.
Results Reference
derived

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Physical Activity in Renal Disease (PAIRED): The Effect on Hypertension

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