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Effectiveness of Text Message-based Rehabilitation Program for Patients With Peripheral Artery Disease

Primary Purpose

Message-based Rehabilitation for Peripheral Artery Disease Patients

Status
Unknown status
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Message-based lifestyle intervention
Sponsored by
Caritas Institute of Higher Education
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Message-based Rehabilitation for Peripheral Artery Disease Patients focused on measuring Rehabilitation, Peripheral artery disease, Mobile phone text message

Eligibility Criteria

50 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Aged above 50 Clinical diagnosis of peripheral artery disease Received revascularization in the past 6 months. Must be able to receive and read Chinese messages from their own mobile phones Must be able to come back for a 6-week and 6-month follow-up for lifestyle counselling and blood sample taking.

Exclusion Criteria:

Refuse to provide an informed-consent form. Clinical diagnosis of lack of capacity to provide informed consent.

Sites / Locations

  • Choy Hau KimRecruiting
  • Choy Hau KimRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

message-based lifestyle intervention

Control

Arm Description

The intervention group will receive 4 mobile phone messages per week for 24 weeks.

no intervention

Outcomes

Primary Outcome Measures

Change of Fasting blood low density lipoprotein (LDL) level
Fasting blood low density lipoprotein (LDL) level

Secondary Outcome Measures

Change of Smoking status
self-reported 7-day point prevalence abstinence and validated by exhaled carbon monoxide monitor (<4 ppm)
Change of Readiness for behavioural changes
Measured by Patient Activation Measure
Change of Health related Quality of life
Measured by SF12v2
Change of BMI
Body Mas Index
Change of ABI
Ankle-Brachial Index
Change of Fasting glucose level
Fasting glucose level
Change of HDL level
HDL level
Change of Total cholesterol level
Total cholesterol level

Full Information

First Posted
August 13, 2018
Last Updated
January 29, 2019
Sponsor
Caritas Institute of Higher Education
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1. Study Identification

Unique Protocol Identification Number
NCT03640767
Brief Title
Effectiveness of Text Message-based Rehabilitation Program for Patients With Peripheral Artery Disease
Official Title
The Effectiveness of Text Message-based Rehabilitation Program on Cardiometabolic Risk Factors for Patients With Peripheral Artery Disease Post-surgical Revascularization: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Unknown status
Study Start Date
December 1, 2018 (Actual)
Primary Completion Date
December 31, 2019 (Anticipated)
Study Completion Date
June 30, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Caritas Institute of Higher Education

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
Background: Many patients with peripheral artery disease are unable to achieve healthy lifestyle after revascularization. There is evidence that rehabilitation program could result in decreased re-admission, reduced cardiometabolic risk factors and improved quality of life. Aim: This first randomized controlled trial to examine the effectiveness of mobile phone text message-based rehabilitation on low density lipoprotein (LDL), Ankle Brachial Index (ABI), healthy lifestyle behaviors and quality of life for patients after revascularization. Methods: This is a 6 months randomized controlled trial. It is hypothesized that message-based rehabilitation program will be effective in improving the low density lipoprotein (LDL), Ankle Brachial Index (ABI), healthy lifestyle behaviors and quality of life for patients with peripheral artery disease after surgical revascularization. A total of 160 participants will be recruited for the study. The participants will be randomly divided into intervention and control groups. Both intervention and control groups will receive face-to-face lifestyle adherence counseling and booklet at baseline. The intervention group will receive 4 mobile phone messages per week for 24 weeks. All participants will be asked to fill in the questionnaires at the baseline, 6-week and 6-month follow-up in Surgical Out Patient Department (SOPD). Participants' blood results of low density lipoprotein (LDL) at the baseline and at 6-month follow-up will be retrieved from Computer Management System in SOPD The primary outcomes are the fasting LDL levels at 6 months. Secondary outcome are Ankle-Brachial Index (ABI), BMI, Fasting glucose level, HDL level, Total cholesterol level, self-reported adherence to healthy lifestyle behaviours, quality of life and smoking status. Participants: The target participants of this study are peripheral artery disease patients who have received revascularization in the Surgical Department of a regional hospital in Hong Kong. The eligible participants are Chinese, aged 50 years or above, and with medical record of peripheral artery disease with revascularization done in the past 6 months. The participants should be able to receive and read Chinese texts from their own mobile phones and are available to come back for a 6-month follow-up for lifestyle counselling. The potential participants will be excluded if they refuse to provide an informed-consent form or if they have medical records stating their lack of capacity to provide informed consent. The recruitment procedure will take place in Department of Surgery in a regional hospital. Study setting: The study will be conducted in the Surgical Department of a regional hospital in Hong Kong.
Detailed Description
Background Peripheral artery disease (PAD) is a circulatory disease which associated with narrowing of arteries in the lower limbs. It is also a common atherosclerotic vascular disease affecting 3-12% of the global population [1]. With aging of the global population and increasing industrialization, PAD is expected to increase further in the next few decades. Worse of all, PAD increases risk of coronary, cerebrovascular complication including death [2]. So secondary prevention is essential for patients with PAD especially after revascularization. There is robust evidence that the secondary prevention of peripheral artery disease can be achieved by lifestyle modification [3-4]. The American Heart Association (AHA) recommended that smoking cessation, glycemic control and structured exercise are import elements of care for patient with PAD [5]. Despite the need of secondary prevention and the evidence-based guidelines from AHA, there is no structured rehabilitation program for PAD patients in Hong Kong. Recent studies reported secondary prevention of PAD mainly focus on exercise and medication therapy. However, a single lifestyle behavioral change could not address the needs of the patients who have multiple lifestyle risk factors. Since many PAD patients have more than one lifestyle risk factor, the rehabilitation program targeting multiple lifestyle behavioral changes will be more benefit to the at risk patients. Mobile-rehabilitation is a new concept to deliver the rehabilitation program. Center-based rehabilitation is well evidenced to reduce mortality, unplanned hospital admissions and improve quality of life and psychological well-being of the patients [6]. However, its benefits is limited by low referral rate and inaccessibility of program site [7]. Mobile phone messaging can be used to motivate and reinforce the lifestyle behavioral changes. It can also prevent patients from relapsing to the previous unhealthy lifestyle behavioral stage. Current studies show a positive result of using texting to promote healthy lifestyle behaviors among adults with cardiovascular disease [8-9]. Considering that the mobile-phone penetration rate in Hong Kong is about 96.1% [10], the use of texting can be an innovative and cost-effective tool to promote a healthy lifestyle and improve quality of life of PAD patients. To the best of the author's knowledge, there have been no Randomized Controlled Trial (RCT) of a stand-alone mobile phone message-based rehabilitation program designed to help peripheral artery disease patients. This is the first randomized controlled trial to examine the effectiveness of message-based rehabilitation on cardiometabolic risk factors for PAD patients who have received surgical revascularization. The transtheorectical model (TTM) [11] will be used as a framework for conceptualizing the process of behavior change. This model is well-suited to this messaging-based intervention as it allows understanding of participants' processes and dynamics of behavioral changes. 2. Aim This single-blinded randomized controlled trial aimed to evaluate the effectiveness of the message-based rehabilitation on fasting low density lipoprotein (LDL) level, Ankle-Brachial Index (ABI), healthy lifestyle behaviours, quality of life and smoking status for PAD patients who have received revascularization. 3. Research hypothesis The research hypothesis is that the message-based rehabilitation program improve the LDL, ABI and the cardiometabolic risk factors of peripheral artery disease (PAD) patients who have received revascularization. 4. Methodology 4.1 Study design This pilot randomised controlled trial aimed at examining the effectiveness of message-based lifestyle intervention. Peripheral artery disease patients who have received revascularization in the past 6 months, are randomized into 2 groups. The total sample size will be 160. Both intervention and control groups will receive face-to-face lifestyle adherence counseling and booklets at baseline. The intervention group will receive 4 mobile phone messages per week for 24 weeks. The messages are motivational advice to support lifestyle behavioral modification in various stages of behavioral changes. All participants will be follow up at 6-week and 6-month in Surgical Out Patient Department. Participants' ABI, lifestyle behaviors and quality of life will be assessed at baseline, 6- week and 6-month follow-up. Participants' fasting low density lipoprotein (LDL) level at baseline and at 6-month follow up will be retrieved from Computer Management System with approval of Dr. Leung Siu-kee, Chief Of Service Department of Surgery Tuen Mun Hospital. At least ten participants from intervention group will be purposively selected for individual face-to-face semi-structured interview to evaluate the mobile phone-based rehabilitation program at 6-month follow-up. 4.2 Study outcomes Primary outcomes: - Fasting blood low density lipoprotein (LDL) level Secondary outcome: Smoking status Readiness for behavioural changes Health related Quality of life Self-reported walking physical exercise (session per week) Self-reported serving fruits and vegetables consumed per day BMI Fasting glucose level HDL level Total cholesterol level ABI 4.3 Study setting The study will be conducted in the Department of Surgery in Tuen Mun Hospital 4.4 Sampling method Probability sampling (simple random sampling) will be adopted for this study. Simple individual randomization method by sequentially numbered, opaque sealed envelopes (SNOSE) will be used to ensure the PI and participants will be concealed from the allocation sequence. The trained research assistant will prepare 160 identical, opaque, sealed, A5-sized envelops, with a unique 3-digit serial number on the cover of each envelope as an identifier. Half of them will each contain a card indicating "intervention" and the other half, " control". After consent, the trained research assistant will open an envelope according to the sequence of the serial number and assign participant to either "intervention" or "control" group. The envelop must be opened according to the serial number. All others will not know the group allocation before the envelope is opened. Frequent checks (at least weekly) of these numbers will be done to ensure no deviation. 4.5 Sample size Sample size will be determined according to power (1-β), type 1 error (α), and effect size. The mean effect size of lifestyle intervention from a previous study is 0.4, which is a medium effect size according to Cohen 1998 [12]. Thus, an effect size of 0.4 was used in the calculations. To achieve the conventional level of 80% power and α= 5%, the sample size will be 128. The attrition rate in previous studies ranged from 16%-20%. A total of 160 participants will ultimately be required; 80 participants will be randomized to either intervention or control group. 4.6 Study intervention The message-based lifestyle intervention consists of three parts. Both the intervention and control groups will receive Parts I and II. Only the intervention group will receive Part III, which is the mobile phone messaging. Part I: Conduct an individualized healthy lifestyle education The first part is face-to-face individual health education with supportive brief counselling. It consists of the identification of lifestyle risk factors and modification strategies for secondary prevention of PAD. This counselling service will be provided by Site Supervisor, Mr. Ng Hoi Wa. A measurable and realistic lifestyle modification plan will be established together with the client and the site supervisor. Part II: Develop a healthy lifestyle booklet The second part is a reinforcement tool for face-to-face education. The research team will develop a booklet includes misconceptions, maladaptive beliefs, facilitators and barriers of healthy lifestyle modification. Part III: Perform mobile phone-based messaging The trained research assistant will deliver the messages to the participants of the intervention group for 24 weeks throughout the study. The messages will act as a reinforcement to increase self-awareness about health-promoting behaviour and develop the desire for competence in achieving a healthy lifestyle. 5. Data collection The quantitative data will be collected by using questionnaires. The trained research assistant will explain the nature and purpose of the research to the potential participants in interview room in Department of Surgery. The eligible participants are requested to sign the informed-consent forms and reminded that their participation is voluntary. The participants are also requested to fill in two questionnaires, Patient Activation Measure [13] & Short Form 12 version 2 (SF12v2) [14], at the baseline, 6-week and 6-month follow-up. The participants' blood result of fasting low density lipoprotein (LDL) level will be retrieved from computer management system in Department of Surgery. Face-to-face individual semi-structured interviews will be conducted to collect qualitative data. 6. Data analysis Quantitative data will be analysed using International Business Machines Corporation(IBM) Statistics is leading statistical software (SPSS) version 22.0 [15]. The descriptive measures of all participants will be summarised by percentage, mean, and 95% confidence interval (CI), as well as compared for between-group differences. The t-test will be conduct to compare the differences in continuous variables between the intervention and control groups. The qualitative data will be audio-recorded and analysed by thematic analysis. Seven open-ended questions will be used in the semi-structured interviews. How do you feel about the mobile phone text message-based rehabilitation? What factors encouraged you to participate in Peripheral Artery Disease Rehabilitation program? What factors discouraged you from participate in Peripheral Artery Disease Rehabilitation program? How did the mobile phone text message-based rehabilitation facilitate your participation in lifestyle modification? How easy did you find following the lifestyle advice from the mobile phone text message? How difficult did you find following the lifestyle advice from mobile phone text message? Any suggestions on how to improve and promote the rehabilitation for patients with peripheral artery disease?

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Message-based Rehabilitation for Peripheral Artery Disease Patients
Keywords
Rehabilitation, Peripheral artery disease, Mobile phone text message

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This pilot randomised controlled trial aimed at examining the effectiveness of message-based lifestyle intervention. Peripheral artery disease patients who have received revascularization in the past 6 months, are randomized into 2 groups. The total sample size will be 160.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
160 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
message-based lifestyle intervention
Arm Type
Experimental
Arm Description
The intervention group will receive 4 mobile phone messages per week for 24 weeks.
Arm Title
Control
Arm Type
No Intervention
Arm Description
no intervention
Intervention Type
Behavioral
Intervention Name(s)
Message-based lifestyle intervention
Intervention Description
Peripheral artery disease patients who have received revascularization in the past 6 months, are randomized into 2 groups. The total sample size will be 160. Both intervention and control groups will receive face-to-face lifestyle adherence counseling and booklets at baseline. The intervention group will receive 4 mobile phone messages per week for 24 weeks. The messages are motivational advice to support lifestyle behavioral modification in various stages of behavioral changes.
Primary Outcome Measure Information:
Title
Change of Fasting blood low density lipoprotein (LDL) level
Description
Fasting blood low density lipoprotein (LDL) level
Time Frame
Change from the baseline and 6-month follow-up.
Secondary Outcome Measure Information:
Title
Change of Smoking status
Description
self-reported 7-day point prevalence abstinence and validated by exhaled carbon monoxide monitor (<4 ppm)
Time Frame
Change from baseline, 6- week and 6-month follow-up
Title
Change of Readiness for behavioural changes
Description
Measured by Patient Activation Measure
Time Frame
Change from baseline, 6- week and 6-month follow-up
Title
Change of Health related Quality of life
Description
Measured by SF12v2
Time Frame
Change from baseline, 6- week and 6-month follow-up
Title
Change of BMI
Description
Body Mas Index
Time Frame
Change from baseline, 6- week and 6-month follow-up
Title
Change of ABI
Description
Ankle-Brachial Index
Time Frame
Change from baseline, 6- week and 6-month follow-up
Title
Change of Fasting glucose level
Description
Fasting glucose level
Time Frame
Change from baseline and 6-month follow-up
Title
Change of HDL level
Description
HDL level
Time Frame
Change from baseline and 6-month follow-up
Title
Change of Total cholesterol level
Description
Total cholesterol level
Time Frame
Change from baseline and 6-month follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged above 50 Clinical diagnosis of peripheral artery disease Received revascularization in the past 6 months. Must be able to receive and read Chinese messages from their own mobile phones Must be able to come back for a 6-week and 6-month follow-up for lifestyle counselling and blood sample taking. Exclusion Criteria: Refuse to provide an informed-consent form. Clinical diagnosis of lack of capacity to provide informed consent.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hau Kim CHOY, MSc
Phone
852 3702 4262
Ext
4262
Email
hkchoy@cihe.edu.hk
First Name & Middle Initial & Last Name or Official Title & Degree
Hoi Wa NG, MSc
Phone
+852 63808505
Email
nhw716@ha.org.hk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hau Kim CHOY, MSc
Organizational Affiliation
Caritas Institute of Higher Education
Official's Role
Principal Investigator
Facility Information:
Facility Name
Choy Hau Kim
City
Hong Kong
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hau Kim CHOY, MSc
Phone
+852 3702 4262
Ext
4262
Email
hkchoy@cihe.edu.hk
First Name & Middle Initial & Last Name & Degree
Hoi Wa NG, MSc
Phone
+852 6380 8505
Email
nhw716@ha.org.hk
First Name & Middle Initial & Last Name & Degree
Po Tai CHAN, PhD
First Name & Middle Initial & Last Name & Degree
Wei Han HUI, MBBS
First Name & Middle Initial & Last Name & Degree
Albert Kit Yu NG, MBBS
First Name & Middle Initial & Last Name & Degree
Hoi Wa NG, MSc
First Name & Middle Initial & Last Name & Degree
Ha Kan CHU, MSc
First Name & Middle Initial & Last Name & Degree
Lisa Pau Le LOW, PhD
First Name & Middle Initial & Last Name & Degree
Hau Kim CHOY, MSc
Facility Name
Choy Hau Kim
City
Hong Kong
State/Province
HK
ZIP/Postal Code
HK
Country
Hong Kong
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hau Kim CHOY, MSc
Phone
+852 3702 4262
Ext
4262
Email
hkchoy@cihe.edu.hk
First Name & Middle Initial & Last Name & Degree
Hoi Wa NG, MSc
Phone
+852 6380 8505
Email
nhw716@ha.org.hk
First Name & Middle Initial & Last Name & Degree
Po Tai CHAN, PhD
First Name & Middle Initial & Last Name & Degree
Wei Han HUI, MBBS
First Name & Middle Initial & Last Name & Degree
Albert Kit Yu NG, MBBS
First Name & Middle Initial & Last Name & Degree
Hoi Wa NG, MSc
First Name & Middle Initial & Last Name & Degree
Ha Kan CHU, MSc
First Name & Middle Initial & Last Name & Degree
Lisa Pau Le LOW, PhD
First Name & Middle Initial & Last Name & Degree
Hau Kim CHOY, MSc

12. IPD Sharing Statement

Plan to Share IPD
No
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Effectiveness of Text Message-based Rehabilitation Program for Patients With Peripheral Artery Disease

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