Effectiveness of a Mobile App for Individuals With or at Risk of Knee Osteoarthritis
Primary Purpose
Knee Pain/Osteoarthritis, Digital Health
Status
Unknown status
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
mRehab app
Sham app
Sponsored by
About this trial
This is an interventional health services research trial for Knee Pain/Osteoarthritis
Eligibility Criteria
Inclusion criteria for all participants:
- at least 50 years of age,
- a regular smartphone user,
- able to speak Cantonese and read Chinese,
- able to perform the exercises required in the physical assessments,
- able to provide written informed consent.
Inclusion criteria for KOA-at-risk participants:
- with subnormal quadriceps strength (as defined by the inability to complete five repetitions of a sit-to-stand test in less than 8 seconds [50 to 70 years of age], 10 seconds [70 to 79 years of age], or 12 seconds [80 years or older])
- with significant chronic knee pain (i.e., β₯2/10 on the 11-point Numerical Pain Rating Scale for more than 3 months on most days of the previous month, aggravated by weight-bearing or movement)
- without regular medical follow-up for knee problems
Inclusion criteria for KOA-diagnosed participants:
- with symptomatic radiographic KOA and being followed-up in hospitals
- have radiographic evidence of grade 2 to 3 KOA on the Kellgren-Lawrence scale in the posteroanterior and/or skyline view or the presence of lateral/posterior osteophytes.
Exclusion criteria:
- have a cognitive impairment,
- have nonambulatory status,
- have systemic inflammatory arthritis (e.g., gout),
- have a history of knee or hip replacement surgery,
- have a history of trauma or surgical arthroscopy of either knee within the past 6 months,
- involve in a similar study,
- participate in a knee exercise program within the past 6 months,
- have an intra-articular injection to the knee within the past 3 months,
- have recent or imminent surgery (within 3 months),
- have medical co-morbidities that preclude participation in exercise
Sites / Locations
- Hong Kong East Cluster, Hospital Authority
- Hong Kong West Cluster, Hospital Authority
- New Territories East Cluster, Hospital Authority
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Sham Comparator
Arm Label
mRehab app
Sham app
Arm Description
Participants randomized to the intervention group will be given the mRehab app free of charge to perform self-management of their knees in their homes.
Participants randomized to the control group will receive a sham app free of charge to perform self-management of their knees in their homes.
Outcomes
Primary Outcome Measures
Changes in knee pain
Knee pain will be assessed on a 11-point Numerical Pain Rating Scale, with 0 representing no pain and 10 representing the worst possible pain.
Changes in physical function of the knee
Physical function will be measured with the 17-item physical function for daily living subscale of the Knee Injury and Osteoarthritis Outcome Score (KOOS). A 5-point Likert scale is used and all items have five possible answer options scored from 0 (No Problems) to 4 (Extreme Problems).
Secondary Outcome Measures
Changes in lower limb function
Lower limb function will be assessed by a 40-m fast-paced walking test, a 9-step stair-climb test, a five-repetition sit-to-stand test, active and passive ranges of motion of the hip and knee joints, and the mini-balance evaluation system test (mini-BESTest).
Changes in lower limb muscle strength
Maximal isometric strength of the quadriceps and hamstrings will be assessed by a handheld dynamometer.
Changes in health-related physical activity
Health-related physical activity will be assessed using the Chinese version of international physical activity questionnaire. This questionnaire asks participants to report the frequency and duration of walking, all vigorous and moderate activities lasting at least 10 min, plus time spent in sedentary activity (sitting and lying awake) during the past 7 days. The data were converted to metabolic equivalent scores for each type of activity, with higher score indicating more physical activity.
Changes in self-efficacy for coping with knee problems
Self-efficacy will be assessed using a 5-item self-efficacy scale modified from an existing validated scale, with scores ranging from 1 (not at all confident) to 10 (totally confident).
Changes in health-related quality of life
Health-related quality of life will be measured using the Chinese version of the EuroQoL 5-dimension 5-level (EQ-5D-5L) questionnaire, which consists of the EuroQoL 5-dimension (EQ-5D) descriptive system and the EQ visual analogue scale (VAS). The EQ-5D descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression; each dimension is rated on a 3-point scale (i.e., no problems, some problems, and extreme problems). The EQ VAS asks the subject to indicate his or her health state on a vertical, visual analog scale with end points of 0 (worst imaginable health state) and 100 (best imaginable health state).
Full Information
NCT ID
NCT04199416
First Posted
December 10, 2019
Last Updated
November 5, 2020
Sponsor
The University of Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT04199416
Brief Title
Effectiveness of a Mobile App for Individuals With or at Risk of Knee Osteoarthritis
Official Title
Effectiveness of an Interactive, Multi-functional Mobile App-based Technology in Endogenous Healthcare for Individuals With or at Risk of Knee Osteoarthritis: A 12-month Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2021 (Anticipated)
Primary Completion Date
March 31, 2023 (Anticipated)
Study Completion Date
March 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Hong Kong
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
To develop and examine an interactive, multi-functional mobile app-based technology designed to encourage endogenous health care using a 12-month randomized controlled trial to demonstrate whether knee osteoarthritis (KOA)-at-risk individuals and KOA-diagnosed patients can improve their knee pain, physical function, and other relevant outcomes by using the technology to support knee/KOA self-management.
Detailed Description
Knee osteoarthritis (KOA), the most common degenerative condition affecting the peripheral weight-bearing joints, leads to pain, restricted mobility, and financial and moral burden. These effects will increase with rising numbers of incidents, exacerbated by population aging and obesity. Zhang et al. found KOA in 43% and 22% (15% and 6% in symptomatic individuals) of Chinese women and men, respectively, 60 years or older. In the United States, KOA affects 12% of the elderly population, and it is projected that the need for total knee replacement (TKR) to treat end-stage KOA will grow by 673% to 3.48 million procedures a year from 2005 to 2030, with the demand for TKR revision doubling from 2005 to 2015. Hong Kong's public hospitals performed 6658 TKRs from 2011 to 2014, with 10,000 cases wait-listed for 2016. These figures suggest that KOA will impose significant and increasing pressure on Hong Kong's healthcare system.
As quadriceps muscle weakness increases the risk of KOA, its symptoms should be alleviated by leg muscle strengthening. Land-based exercise has been effective under close monitoring and supervision. A recent Cochrane Review involving 54 studies concluded that there is moderate to high-quality evidence that land-based exercises significantly improve muscle strength, physical function, and quality of life and reduce pain in KOA patients. The effect of such exercises is comparable to that of nonsteroidal anti-inflammatory drugs with no significant adverse effects. However, therapist-delivered exercise is costly and often impractical, especially in a public-health context, and Internet-delivered exercise regimes represent an alternative approach. In today's information technology (IT)-enabled environment, mobile apps are readily accessible to users of untethered devices (e.g., smartphones). The "any-where, any-time" mobile IT could be exploited to more effectively manage KOA by encouraging self-motivation to substitute for direct monitoring. This study will present "IT-centered endogenous healthcare" as a public policy to boost self-help in primary care and test its practicability and efficacy in KOA management in Hong Kong. The word "endogenous" suggests that self-motivation is a form of self-insurance in primary care. It is further suggested that demand-side incentives will be needed to induce individuals to incrementally allocate more resources (particularly time and effort) to incrementally self-insure health at the primary level.
On the supply side, IT-based healthcare products have been mainly designed for commercial considerations such as marketing and are insufficiently focused on function for purposes of public health and policy. We follow Liao-Cheung's approach to reify demand-side incentives in the form of a publicly funded (and hence free) mobile app, the adoption of which could encourage self-insurance among individuals with knee problems or KOA. The users' time and effort will initially be rewarded by the app's user-friendliness and lack of a fee. The study's technology intervention, "mobile rehabilitation (mRehab) app", will link smartphones to videos of evidence-based, physiotherapist-prescribed exercises to alleviate knee/KOA symptoms, together with educational (e.g., diet and behavioral modifications) and motivational components. This mobile IT platform will have easier and wider accessibility than exercises delivered via tethered devices (e.g., desktop computers), and it can engage the users' interest whenever and wherever KOA effects are felt. Over time, self-motivation is also enhanced by high-frequency prompts, periodic upgrades with feedback, support from Internet KOA-awareness groups, the possibility of accumulating one's own health-data to facilitate queries and dialogue, and (most importantly) monitoring the health progression predicted by the exercise regimen.
A natural research sample follows in the form of IT-enabled individuals with knee/KOA problems. The proposed hypothesis is then offered that sustained use of the mRehab app will significantly reduce the symptoms and improve functions of individuals with quadriceps weakness and knee pain or KOA over time and compared to a sham app (the analytical control). The effectiveness of the mRehab app regarding this hypothesis will be tested in two samples: (1) KOA-at-risk individuals and (2) KOA-diagnosed patients, in a randomized controlled trial (RCT).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Pain/Osteoarthritis, Digital Health
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
320 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
mRehab app
Arm Type
Experimental
Arm Description
Participants randomized to the intervention group will be given the mRehab app free of charge to perform self-management of their knees in their homes.
Arm Title
Sham app
Arm Type
Sham Comparator
Arm Description
Participants randomized to the control group will receive a sham app free of charge to perform self-management of their knees in their homes.
Intervention Type
Device
Intervention Name(s)
mRehab app
Intervention Description
The mRehab app will be an interactive system with a user-friendly graphical user interface to provide multiple motivational functions that engage individuals in their prescribed home exercises. The app will contain video-based lower limb strengthening and aerobic exercise materials, health information, and motivational functions to increase their access to rehabilitation and care resources to augment their self-management ability.
Intervention Type
Device
Intervention Name(s)
Sham app
Intervention Description
The sham app will only contain educational components and text-based exercise recommendations.
Primary Outcome Measure Information:
Title
Changes in knee pain
Description
Knee pain will be assessed on a 11-point Numerical Pain Rating Scale, with 0 representing no pain and 10 representing the worst possible pain.
Time Frame
from baseline to 3, 6, 9, and 12 months
Title
Changes in physical function of the knee
Description
Physical function will be measured with the 17-item physical function for daily living subscale of the Knee Injury and Osteoarthritis Outcome Score (KOOS). A 5-point Likert scale is used and all items have five possible answer options scored from 0 (No Problems) to 4 (Extreme Problems).
Time Frame
from baseline to 3, 6, 9, and 12 months
Secondary Outcome Measure Information:
Title
Changes in lower limb function
Description
Lower limb function will be assessed by a 40-m fast-paced walking test, a 9-step stair-climb test, a five-repetition sit-to-stand test, active and passive ranges of motion of the hip and knee joints, and the mini-balance evaluation system test (mini-BESTest).
Time Frame
from baseline to 3, 6, 9, and 12 months
Title
Changes in lower limb muscle strength
Description
Maximal isometric strength of the quadriceps and hamstrings will be assessed by a handheld dynamometer.
Time Frame
from baseline to 3, 6, 9, and 12 months
Title
Changes in health-related physical activity
Description
Health-related physical activity will be assessed using the Chinese version of international physical activity questionnaire. This questionnaire asks participants to report the frequency and duration of walking, all vigorous and moderate activities lasting at least 10 min, plus time spent in sedentary activity (sitting and lying awake) during the past 7 days. The data were converted to metabolic equivalent scores for each type of activity, with higher score indicating more physical activity.
Time Frame
from baseline to 3, 6, 9, and 12 months
Title
Changes in self-efficacy for coping with knee problems
Description
Self-efficacy will be assessed using a 5-item self-efficacy scale modified from an existing validated scale, with scores ranging from 1 (not at all confident) to 10 (totally confident).
Time Frame
from baseline to 3, 6, 9, and 12 months
Title
Changes in health-related quality of life
Description
Health-related quality of life will be measured using the Chinese version of the EuroQoL 5-dimension 5-level (EQ-5D-5L) questionnaire, which consists of the EuroQoL 5-dimension (EQ-5D) descriptive system and the EQ visual analogue scale (VAS). The EQ-5D descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression; each dimension is rated on a 3-point scale (i.e., no problems, some problems, and extreme problems). The EQ VAS asks the subject to indicate his or her health state on a vertical, visual analog scale with end points of 0 (worst imaginable health state) and 100 (best imaginable health state).
Time Frame
from baseline to 3, 6, 9, and 12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria for all participants:
at least 50 years of age,
a regular smartphone user,
able to speak Cantonese and read Chinese,
able to perform the exercises required in the physical assessments,
able to provide written informed consent.
Inclusion criteria for KOA-at-risk participants:
with subnormal quadriceps strength (as defined by the inability to complete five repetitions of a sit-to-stand test in less than 8 seconds [50 to 70 years of age], 10 seconds [70 to 79 years of age], or 12 seconds [80 years or older])
with significant chronic knee pain (i.e., β₯2/10 on the 11-point Numerical Pain Rating Scale for more than 3 months on most days of the previous month, aggravated by weight-bearing or movement)
without regular medical follow-up for knee problems
Inclusion criteria for KOA-diagnosed participants:
with symptomatic radiographic KOA and being followed-up in hospitals
have radiographic evidence of grade 2 to 3 KOA on the Kellgren-Lawrence scale in the posteroanterior and/or skyline view or the presence of lateral/posterior osteophytes.
Exclusion criteria:
have a cognitive impairment,
have nonambulatory status,
have systemic inflammatory arthritis (e.g., gout),
have a history of knee or hip replacement surgery,
have a history of trauma or surgical arthroscopy of either knee within the past 6 months,
involve in a similar study,
participate in a knee exercise program within the past 6 months,
have an intra-articular injection to the knee within the past 3 months,
have recent or imminent surgery (within 3 months),
have medical co-morbidities that preclude participation in exercise
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kalun Or, PhD
Phone
852-39172587
Email
klor@hku.hk
Facility Information:
Facility Name
Hong Kong East Cluster, Hospital Authority
City
Hong Kong
Country
Hong Kong
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yin Chun Loretta YAM
Phone
2595-6411
Email
yamyc@ha.org.hk
Facility Name
Hong Kong West Cluster, Hospital Authority
City
Hong Kong
Country
Hong Kong
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ping-keung CHAN, PhD
Phone
2255-4654
Email
cpk464@ha.org.hk
Facility Name
New Territories East Cluster, Hospital Authority
City
Hong Kong
Country
Hong Kong
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kevin Ki-wai HO, PhD
Phone
3505-2715
Email
kevinho@cuhk.edu.hk
12. IPD Sharing Statement
Plan to Share IPD
No
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Effectiveness of a Mobile App for Individuals With or at Risk of Knee Osteoarthritis
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