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The Effect of Physical ACtivity Enhancement Scheme (PACES) in Hemodialysis Patients

Primary Purpose

Kidney Failure, Chronic, Exercise, Physical Activity

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
PACES intervention
Usual care with sham intervention
Sponsored by
Health Science Center of Xi'an Jiaotong University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Kidney Failure, Chronic focused on measuring End-Stage Renal Disease, Exercise, Physical Activity, Hemodialysis

Eligibility Criteria

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

Inclusion Criteria: adult (age≥18) with stable ESRD; receiving≥3 months HD; receiving HD more than 5 times every two weeks; volunteer for participating in this investigation. Exclusion Criteria: are unable to do walk on one's own (severe musculoskeletal pain at rest or with minimal activity precluding walking or stationary cycling; unable to sit, stand or walk unassisted, walking devices such as cane or walker allowed); have shortness of breath at rest or with activities of daily living (NYHA Class IV); have mental disease, disturbance of consciousness and couldn't cooperate with this investigation.

Sites / Locations

  • Nursing School of the Air Force Medical University

Arms of the Study

Arm 1

Arm 2

Arm Type

Sham Comparator

Experimental

Arm Label

Usual care with sham intervention

PACES intervention

Arm Description

Patients in the control group received usual care with sham exercise.

PACES includes an exercise perception intervention and an exercise intervention, which lasts for 12 weeks and is carried out simultaneously.

Outcomes

Primary Outcome Measures

daily steps (paces)
OMRON electronic pedometer (HJ-321) records the participants' daily steps. Participants are instructed to wear the pedometer on their waist for 7 days, and the pedometer is removed only during rest, bathing and swimming.
The Human Activity Profile (HAP)
HAP is a questionnaire designed to assess general physical activity. It consists of a list of 94 activities ranked in ascending order of level of energy required to perform each activity. Two scores are available from the HAP: a maximum activity score (MAS), reflective of the most taxing activity a respondent is still performing and an adjusted activity score (AAS), reflective of the respondent's daily activity level. The MAS is the number of the highest ranked activity the respondent is still performing. The AAS is calculated by subtracting from the MAS the number of activities that the respondent has stopped performing that rank below the participants' most metabolically intense activity. The minimum and maximum values of MAS and AAS are 0 and 94 respectively. The higher the score, the stronger the physical activity of the patient.

Secondary Outcome Measures

Dialysis Patient-perceived Exercise Benefits and Barriers Scale (DPEBBS)
The 24-item DPEBBS is used to evaluate participants' perceived benefits and barriers to exercise. The scale consisted of 24 items and 2 open questions, including 12 items of exercise benefits and 12 items of exercise barriers. Total scores ranged from 24 to 96. The higher the score, the more exercise benefits the patients experienced and the fewer factors that prevented them from exercise.
Self-efficacy for exercise scale (SEE)
SEE is used to identify the participants' confidence in their ability to exercise, which is a major determinant in the success of changing behavior. The score ranges from 0 to 100, and the higher the score, the higher the level of self-efficacy.
Social support Rating Scale (SSRS)
Participants' social support status is measured by the SSRS. The scale has 10 items, including 3 aspects, objective support, subjective support and utilization of social support. The total score is the sum of points for each item. The higher the score is, the higher the degree of social support is. The scale scores range from 12 to 66, with ≤22 being low, 23 to 44 medium, and 45 to 66 high.
Stage of Change Questionnaire
The questionnaire identifies the participants' state of readiness to adopt a more active lifestyle according to the Health Action Process Approach. The higher the stage, the better the readiness of the participants.
Kidney Disease Quality of Life (KDQOL-36)
KDQOL-36, consisted of the 12-item Short Form Health Survey (SF-12) including the physical component summary (PCS) and the mental component summary (MCS) and 24 disease-specific items which entail 3 subscales: the symptom and problems list, the burden of kidney disease, and the effects of kidney disease, is to evaluate patients' QoL. Scores of each dimension range from 0 to 100 and higher scores represent better QoL.
Glomerular filtration rate (GFR)
GFR is estimated by the using the CKD-EPI creatinine equation.
Serum levels of IL-6
Serum levels of IL-6 is measured using immunoassay kit (DuoSet ELISA Development, R&D Systems, Inc., USA). Blood samples are drawn after an overnight fast of at least 12 hour. The last blood collection will be performed 48 h after the last exercise session, to avoid acute effects of the exercise influencing inflammatory and oxidative stress markers. These methods will follow the manufacturer's recommendations.
C-reactive protein (CRP)
CRP is evaluated as an index of catabolism and systemic inflammation using a high-sensitivity assay.
Serum creatinine
Serum creatinine is evaluated as an index of catabolism and systemic inflammation.
sit-to-stand tests 10 (STS-10)
The sit-to-stand tests 10(STS-10) is a test that assesses the capacity to stand up from a chair. The STS-10 is calculated as the total time needed to complete 10 repetitions of standing up and sitting down again.
sit-to-stand tests 60 (STS-60)
The sit-to-stand tests 60 (STS-60) is a test that assesses the capacity to stand up from a chair. The STS-60 registers the repetitions performed in 60 seconds.
Six-minute walk test (6MWT)
6MWT is commonly used to assess walking capacity in patients with chronic diseases, including Chronic Kidney Disease (CKD) patients.
Ejection fraction
Transthoracic echocardiography is performed using a Vivid E95 ultrasound system (General Electric, Frankfurt, Germany) equipped with a multifrequency transducer and 4D imaging analysis software. Normative ultrasound images were obtained by use of a 3.5-MHz phased array probe, placed on the third or fourth left intercostal space and Apical region. Connect electrocardiogram (ECG) for each subject to ensure standardization of image acquisition and data calculation to obtain ejection fraction. Data were analyzed and interpreted by one experienced echocardiographer who was blinded to treatment status and imaging sequence. To minimize the effect of variations in fluid volume in hemodialysis patients, studies were performed 18-24 h after a hemodialysis session.
Left ventricular mass index
Left ventricular mass is calculated from M-mode images, according to the guidelines of the American Society of Echocardiography. The left ventricular mass index is obtained by dividing by the formula of body surface area.
Left ventricular volume index
Left ventricular volume is calculated from M-mode images, according to the guidelines of the American Society of Echocardiography. The left ventricular volume index is obtained by dividing by the formula of body surface area. index is obtained by dividing by the formula of body surface area.

Full Information

First Posted
December 24, 2022
Last Updated
January 30, 2023
Sponsor
Health Science Center of Xi'an Jiaotong University
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1. Study Identification

Unique Protocol Identification Number
NCT05718765
Brief Title
The Effect of Physical ACtivity Enhancement Scheme (PACES) in Hemodialysis Patients
Official Title
The Effect of Physical ACtivity Enhancement Scheme (PACES) on Physical Outcomes in Hemodialysis Patients
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Completed
Study Start Date
September 20, 2022 (Actual)
Primary Completion Date
January 10, 2023 (Actual)
Study Completion Date
January 10, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Health Science Center of Xi'an Jiaotong University

4. Oversight

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

5. Study Description

Brief Summary
Hemodialysis is the most commonly used renal replacement therapy for end-stage renal disease (ESRD) patients. At present, more than 553,000 ESRD patients in China are receiving hemodialysis treatment, but the long-term survival rate is low, and the annual mortality rate is as high as 18%. This is significantly related to lower physical activity in hemodialysis patients. Physical inactivity can lead to the decline of cardiopulmonary function and muscle function, the aggravation of daily life restriction and the increased risk of death. The National Kidney Foundation Disease Outcomes Quality Initiative (K/DOQI) recommends physical activity as cornerstone of ESRD rehabilitation. But hemodialysis patients are still living in a physical inactivity state. In the early stage of this study, the Physical Activity Enhancement Scheme (PACES) was developed for hemodialysis patients, that is, taking spaces as the core of physical activity investigation, and encouraging patients to start to improve physical activity. The PACES has been registered on the ClinicalTrials.gov before (number: NCT05189795). The investigators now plan to evaluate the impact of PACES on physical activity of hemodialysis patients through clinical trials.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Kidney Failure, Chronic, Exercise, Physical Activity, Renal Dialysis
Keywords
End-Stage Renal Disease, Exercise, Physical Activity, Hemodialysis

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Usual care with sham intervention
Arm Type
Sham Comparator
Arm Description
Patients in the control group received usual care with sham exercise.
Arm Title
PACES intervention
Arm Type
Experimental
Arm Description
PACES includes an exercise perception intervention and an exercise intervention, which lasts for 12 weeks and is carried out simultaneously.
Intervention Type
Behavioral
Intervention Name(s)
PACES intervention
Intervention Description
The exercise perception intervention program is divided into three stage, and every four weeks is a stage. The theme of the first stage is to make the patient have the intention to exercise. The theme of the second stage is to provide effective support for the patient, so that the patient can take the initiative to start exercise. The theme of the third stage is to enable patients to keep exercising. The exercise intervention is a 12-week progressive intradialytic combined cycling exercise which proceed in the first HD 2 hours for safety. Each session consisted of a 5-minute warm-up, cool-down and 30-minute cycling at a Rating of Perceived Exertion (RPE) of 12-14. The machine has two exercise types including aerobic exercise and resistance exercise. Every four weeks is divided into a stage. And the time of aerobic exercise and resistance exercise were personally adjusted per stage to maintain the personalized target RPE.
Intervention Type
Other
Intervention Name(s)
Usual care with sham intervention
Intervention Description
Patients in the control group received usual care and were advised to do sham exercise such as stretch legs and arms about 15 minutes during the first 2 hemodialysis hours.
Primary Outcome Measure Information:
Title
daily steps (paces)
Description
OMRON electronic pedometer (HJ-321) records the participants' daily steps. Participants are instructed to wear the pedometer on their waist for 7 days, and the pedometer is removed only during rest, bathing and swimming.
Time Frame
Change from daily steps at 12 weeks.
Title
The Human Activity Profile (HAP)
Description
HAP is a questionnaire designed to assess general physical activity. It consists of a list of 94 activities ranked in ascending order of level of energy required to perform each activity. Two scores are available from the HAP: a maximum activity score (MAS), reflective of the most taxing activity a respondent is still performing and an adjusted activity score (AAS), reflective of the respondent's daily activity level. The MAS is the number of the highest ranked activity the respondent is still performing. The AAS is calculated by subtracting from the MAS the number of activities that the respondent has stopped performing that rank below the participants' most metabolically intense activity. The minimum and maximum values of MAS and AAS are 0 and 94 respectively. The higher the score, the stronger the physical activity of the patient.
Time Frame
Change from HAP 12 weeks.
Secondary Outcome Measure Information:
Title
Dialysis Patient-perceived Exercise Benefits and Barriers Scale (DPEBBS)
Description
The 24-item DPEBBS is used to evaluate participants' perceived benefits and barriers to exercise. The scale consisted of 24 items and 2 open questions, including 12 items of exercise benefits and 12 items of exercise barriers. Total scores ranged from 24 to 96. The higher the score, the more exercise benefits the patients experienced and the fewer factors that prevented them from exercise.
Time Frame
DPEBBS is measured at baseline (before intervention) and after 12 weeks of intervention.
Title
Self-efficacy for exercise scale (SEE)
Description
SEE is used to identify the participants' confidence in their ability to exercise, which is a major determinant in the success of changing behavior. The score ranges from 0 to 100, and the higher the score, the higher the level of self-efficacy.
Time Frame
SEE is measured at baseline (before intervention) and after 12 weeks of intervention.
Title
Social support Rating Scale (SSRS)
Description
Participants' social support status is measured by the SSRS. The scale has 10 items, including 3 aspects, objective support, subjective support and utilization of social support. The total score is the sum of points for each item. The higher the score is, the higher the degree of social support is. The scale scores range from 12 to 66, with ≤22 being low, 23 to 44 medium, and 45 to 66 high.
Time Frame
SSRS is measured at baseline (before intervention) and after 12 weeks of intervention.
Title
Stage of Change Questionnaire
Description
The questionnaire identifies the participants' state of readiness to adopt a more active lifestyle according to the Health Action Process Approach. The higher the stage, the better the readiness of the participants.
Time Frame
The questionnaire is measured at baseline (before intervention) and after 12 weeks of intervention.
Title
Kidney Disease Quality of Life (KDQOL-36)
Description
KDQOL-36, consisted of the 12-item Short Form Health Survey (SF-12) including the physical component summary (PCS) and the mental component summary (MCS) and 24 disease-specific items which entail 3 subscales: the symptom and problems list, the burden of kidney disease, and the effects of kidney disease, is to evaluate patients' QoL. Scores of each dimension range from 0 to 100 and higher scores represent better QoL.
Time Frame
KDQOL-36 is measured at baseline (before intervention) and after 12 weeks of intervention.
Title
Glomerular filtration rate (GFR)
Description
GFR is estimated by the using the CKD-EPI creatinine equation.
Time Frame
GFR is measured at baseline (before intervention) and after 12 weeks of intervention.
Title
Serum levels of IL-6
Description
Serum levels of IL-6 is measured using immunoassay kit (DuoSet ELISA Development, R&D Systems, Inc., USA). Blood samples are drawn after an overnight fast of at least 12 hour. The last blood collection will be performed 48 h after the last exercise session, to avoid acute effects of the exercise influencing inflammatory and oxidative stress markers. These methods will follow the manufacturer's recommendations.
Time Frame
Serum levels of IL-6 is measured at baseline (before intervention) and after 12 weeks of intervention.
Title
C-reactive protein (CRP)
Description
CRP is evaluated as an index of catabolism and systemic inflammation using a high-sensitivity assay.
Time Frame
CRP is measured at baseline (before intervention) and after 12 weeks of intervention.
Title
Serum creatinine
Description
Serum creatinine is evaluated as an index of catabolism and systemic inflammation.
Time Frame
Serum creatinine is measured at baseline (before intervention) and after 12 weeks of intervention.
Title
sit-to-stand tests 10 (STS-10)
Description
The sit-to-stand tests 10(STS-10) is a test that assesses the capacity to stand up from a chair. The STS-10 is calculated as the total time needed to complete 10 repetitions of standing up and sitting down again.
Time Frame
STS-10 is measured at baseline (before intervention) and after 12 weeks of intervention.
Title
sit-to-stand tests 60 (STS-60)
Description
The sit-to-stand tests 60 (STS-60) is a test that assesses the capacity to stand up from a chair. The STS-60 registers the repetitions performed in 60 seconds.
Time Frame
STS-60 is measured at baseline (before intervention) and after 12 weeks of intervention.
Title
Six-minute walk test (6MWT)
Description
6MWT is commonly used to assess walking capacity in patients with chronic diseases, including Chronic Kidney Disease (CKD) patients.
Time Frame
6MWT is measured at baseline (before intervention) and after 12 weeks of intervention.
Title
Ejection fraction
Description
Transthoracic echocardiography is performed using a Vivid E95 ultrasound system (General Electric, Frankfurt, Germany) equipped with a multifrequency transducer and 4D imaging analysis software. Normative ultrasound images were obtained by use of a 3.5-MHz phased array probe, placed on the third or fourth left intercostal space and Apical region. Connect electrocardiogram (ECG) for each subject to ensure standardization of image acquisition and data calculation to obtain ejection fraction. Data were analyzed and interpreted by one experienced echocardiographer who was blinded to treatment status and imaging sequence. To minimize the effect of variations in fluid volume in hemodialysis patients, studies were performed 18-24 h after a hemodialysis session.
Time Frame
Ejection fraction is measured at baseline (before intervention) and after 12 weeks of intervention.
Title
Left ventricular mass index
Description
Left ventricular mass is calculated from M-mode images, according to the guidelines of the American Society of Echocardiography. The left ventricular mass index is obtained by dividing by the formula of body surface area.
Time Frame
Left ventricular mass index is measured at baseline (before intervention) and after 12 weeks of intervention.
Title
Left ventricular volume index
Description
Left ventricular volume is calculated from M-mode images, according to the guidelines of the American Society of Echocardiography. The left ventricular volume index is obtained by dividing by the formula of body surface area. index is obtained by dividing by the formula of body surface area.
Time Frame
Left ventricular volume index is measured at baseline (before intervention) and after 12 weeks of intervention.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: adult (age≥18) with stable ESRD; receiving≥3 months HD; receiving HD more than 5 times every two weeks; volunteer for participating in this investigation. Exclusion Criteria: are unable to do walk on one's own (severe musculoskeletal pain at rest or with minimal activity precluding walking or stationary cycling; unable to sit, stand or walk unassisted, walking devices such as cane or walker allowed); have shortness of breath at rest or with activities of daily living (NYHA Class IV); have mental disease, disturbance of consciousness and couldn't cooperate with this investigation.
Facility Information:
Facility Name
Nursing School of the Air Force Medical University
City
Xi'an
State/Province
Shaan XI
Country
China

12. IPD Sharing Statement

Learn more about this trial

The Effect of Physical ACtivity Enhancement Scheme (PACES) in Hemodialysis Patients

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