Rehabilitation Technologies for Chronic Conditions: Will We Sink or Swim?
Abstract
:1. Introduction
2. Materials and Methods
3. Clinical Need in the Populations of Interest
3.1. Neurological Conditions: (e.g., Stroke, Degenerative Conditions, Spinal Cord Injury, and Vestibular Disorders)
3.2. Musculoskeletal Conditions (e.g., Chronic Pain and Arthritis)
3.3. Metabolic Conditions (e.g., Diabetes)
3.4. Pulmonary Conditions (e.g., Chronic Obstructive Pulmonary Disease)
3.5. Cardiovascular Conditions: (e.g., Heart Disease)
4. Technology Review and Efficacy
4.1. Robotic Exoskeletons
4.1.1. Technology Features
4.1.2. Efficacy
Author | Study Design | Population | Intervention | Outcome |
---|---|---|---|---|
Stroke | ||||
Calafiore et al. [43] | Systematic review | Stroke (n = 14 studies, 576) | Lokomat end-effector trainer and exoskeleton | Two studies of exoskeletons showed improvements in walking; poor to good quality studies |
Hsu et al. [7] | Systematic review with meta-analysis | Stroke (n = 13 studies; 492 subjects) 1.2–75 months post-stroke Mixed ambulatory status | Exoskeleton-assisted training compared to dose-matched conventional training 10–40 sessions, 10 days–10 weeks; 150–1800 min | Improved outcomes with exo-training: walking speed [MD] 0.13 m/s, 95% CI (0.05; 0.21), balance [SMD] 0.3, 95% CI (0.07, 0.54); after follow-up, mobility [SMD] 0.45, 95% CI (0.07, 0.84) and endurance [SMD] 46.23 m, 95% CI (9.90, 82.56) |
Karunakaran et al. [6] | Systematic review | Adults with acquired brain injury (n = 45 studies of stroke); total subjects not reported) | Lower extremity robotic exoskeleton for overground walking 1–40 sessions | Generally improved balance gait characteristics; motor impairments but some inconsistencies; no effect on global disability or spasticity |
Leow et al. [8] | Systematic review with meta-analysis | Stroke (n = 20 studies; 759 subjects) | Exoskeleton-assisted training compared to conventional training 2–5x/week; 10 days–10 weeks 20–120 min/session | Improved exo-training: walking ability (d = 0.21; 95% CI (0.01–0.42)); follow-up (d = 0.37; 95% CI (0.03, 0.71)); and walking speed (d = 0.23; 95% CI (0.01–0.46)) Nine studies examined follow-up 22 weeks–12 months |
Parkinson’s Disease | ||||
Carmignano et al. [44] | Systematic review | Parkinson’s disease (n = 20 studies) | Exoskeleton-assisted training (n = 9 studies); end-effector robots (n = 11 studies) 2–5 sessions per week; 3–5 weeks; 20–45 min | Improved gait but not superior to conventional treatment, except in more severe disease No adverse outcomes Quality appraisal low to high |
Picelli et al. [45] | Systematic review | Parkinson’s disease (n = 18 studies); | Exoskeleton-assisted training n = 9 studies; end-effector robots (n = 9 studies) 10–20 sessions over 2–5x/week, 20–40 min duration per session | Improved balance and less freezing of gait Moderate quality studies |
Multiple Sclerosis | ||||
Bowman et al. [46] | Systematic review | Multiple sclerosis (n = 12 studies) | Exoskeleton (n = 10 studies) 6–40 sessions, 2–5 sessions, 3–8 weeks | Improved balance and gait Fair to good study quality, 65% good to excellent study quality |
Calabro et al. [47] | Systematic review | Multiple sclerosis (17 studies) | Lokomat grounded robotic device (n = 13), power exoskeleton (n = 2), end-effector (n = 2) 2–5 sessions/week, 3–18 weeks | Improved gait speed, balance, and endurance; more severe patients improved functional outcomes when paired with VR; improved spasticity, fatigue, pain, psychological wellbeing, and quality of life |
Spinal Cord Injuries | ||||
Hayes et al. [49] | Systematic review | Spinal cord injuries (n = 12 studies; 521 subjects) ASIA scores A-D | Exoskeletons (n = 3), Locomat (n = 9) 11–41 sessions, over 4–24 weeks | No improvements in gait speed compared to conventional training; low to high study quality |
Zhang et al. [50] | Systematic review | Spinal cord injury (n = 11 case-control studies) Complete and incomplete injury ASIA 1A–5A | Power exoskeletons 2–5 sessions/week 30–90 min 1 month–1 year | Improved gait; low study quality and hetereogeneity |
Mixed Neurological Conditions | ||||
Dijkers et al. [48] | Review of systematic reviews | Neurologic populations (n = 17 studies) (stroke, SCI) | Powered exoskeletons for gait training Intervention dosing not provided | Systematic reviews poor-quality; failure to report important clinical characteristics; caution is warranted for decisions on technology use |
Musculoskeletal | ||||
McGibbon et al. [51] | Randomized control trial | Knee osteoarthritis (n = 24 subjects two-stage cross-over design) | Exoskeleton in clinic and home training 2-week use of device at home; 2 weeks of non-use | No immediate effects; improved stair time (p = 0.001), WOMAC pain (p = 0.004), and function (p = 003) |
Diabetes/COPD/Heart Disease | ||||
No studies found |
4.2. Virtual and Augmented Reality
4.2.1. Technology Features
4.2.2. Efficacy
4.3. Remote Monitoring
4.3.1. Technology Features
4.3.2. Efficacy
Author | Study Design | Population | Intervention | Outcome |
---|---|---|---|---|
Neurological Conditions (Stroke and Parkinson’s Disease) | ||||
Stroke | ||||
Dorsch et al. [77] | Randomized control trial | Stroke (n = 135); 11 countries, in-patient acute care setting | Wearable sensors for walking; effects of quantitative feedback on daily walking Monitoring throughout day, 5–7 days/week, with 3x/week feedback, duration mean of 22.5 days | No effect: augmented feedback did not increase time walking, but was useful for therapists |
Lynch et al. [75] | Systematic review | Stroke (n = 4 studies, 245 subjects), time post-stroke 1 week to 51 months | Wearable sensors Variable monitoring rate, inconsistent reporting on time and frequency 30 min–1 h/day, 3x/week, duration 11 days–12 weeks | No effect on step count; low-quality evidence |
Parkinson’s Disease | ||||
Ozden et al. [76] | Systematic review and meta-analysis | Parkinson’s disease (n = five studies, two in meta-analysis) | Varied approaches (mobile apps and/or sensors) Inconsistent reporting frequency and time, duration 6 weeks–12 months | Sensors plus apps were equivalent to standard treatment in balance and function Sensors plus apps improved quality of life and adherence compared to standard treatment. Good quality studies with low–high risk of bias |
Musculoskeletal Conditions | ||||
Christiansen et al. [78] | Randomized control trial | Total knee replacement (n = 43 subjects) | Fitbit, step goals, and one phone call with standard care Continuous monitoring with one call/month, duration 6 months | Intervention increased step count, time walking, and engagement in moderate to vigorous physical activity compared to control |
Mehta et al. [79] | Randomized control trial | Hip and knee arthroplasty (n = 147 subjects) | Wearable activity monitoring Daily monitoring and messaging 1–3x/week. Duration 45 days | No effects on discharge, return to activity; remote monitoring decreased readmission |
Diabetes | ||||
Michaud et al. [80] | Systematic review + meta-analysis | Diabetes (n = 17 studies, 15 studies for meta-analysis) | Telemonitoring devices Duration 3–12 months | Small reduction in HbA1c and weight loss compared to usual care. Subgroup analysis suggested telemonitoring with automatic mobile transmission or with real-time feedback modality may lead to a greater improvement in HbA1c outcomes when compared with telemonitoring without these features. Low- to high-quality |
Chronic Obstructive Pulmonary Disease (COPD) | ||||
Benzo et al. [81] | RCT | COPD (n = 375) | Home-based rehabilitation with remote monitoring and health coaching intervention Continuous monitoring with weekly calls. Exercise included three exercises daily, 6 days/week. Duration 12 weeks | Significant and clinically meaningful difference between the intervention and control in terms of physical and emotional disease specific quality of life scores (95% confidence interval): 0.54 points (0.36–0.73), p < 0.001; 0.51 (0.39–0.69), p < 0.001. |
Zanaboni et al. [82] | RCT | COPD (n = 120) | Telerehabilitation and treadmill training with self-management website that is remotely monitored by physiotherapists. Three groups: (1) Telerehab and treadmill program supervised by PT (2) unsupervised treadmill training with exercise diary, booklet, and individualized training program, and (3) usual care Weekly monitoring, 30-min sessions 3–5 times/week exercise Moderate- to high-intensity. Duration 8 weeks | Significant decrease in hospitalizations and emergency department visits in intervention groups compared to usual care. Significant improvement in COPD health status (p = 0.002) and strength compared to control group (p = 0.027). No differences between groups were detected for self-efficacy, anxiety, and depression scores. |
Stamenova et al. [83] | RCT | COPD (n = 122) | Three groups: (1) remote monitoring by respiratory therapist, (2) self-monitoring, and (3) standard care Monitoring: oxygen saturation, blood pressure, temperature, weight, and symptoms Duration 6 months | No significant difference between groups in self-management, knowledge, symptoms, or healthcare use. |
Heart disease | ||||
Zhong et al. [84] | Systematic review with meta-analysis | Percutaneous coronary surgery recovery (n = 5 studies, 585 subjects) | Home-based cardiac telerehabilitation with remote monitoring 1–5x/week, inconsistent reporting of time and intensity, duration 6–24 weeks | Improve physical exercise capacity (6WMT), systolic blood pressure, triglycerides, and low-density lipoprotein cholesterol compared to control. No effect on quality of life, diastolic blood pressure, total cholesterol, and high-density lipoprotein cholesterol. High variability of intervention models |
Ramachandran et al. [85] | Systematic review + meta-analysis | Heart disease (cardiac rehab phase 2) (n = 14 studies, 2869 subjects) | Home-based cardiac telerehabilitation. Three groups: (1) home-based cardiac telerehabilitation, (2) usual care, (3) clinic cardiac rehabilitation Session monitoring, 1–5x/week, duration 6 weeks–6 months | When compared with usual care, home-based cardiac rehab showed significant improvement in functional capacity, daily step count, exercise habits, depression scores, and quality of life (short-form mental component summary and physical component summary scores). Home-based rehab and clinic-based cardiac rehab were comparably effective on functional capacity physical activity behavior, hospitalizations, and quality of life. Variable risk of bias |
Nick et al. [86] | Systematic review | Heart failure (n = 12 studies, 1923 subjects) | Telemonitoring for improving self-care behaviors Frequency of user interface with device varied between 2x/day and 1x/week for 2–18 months | Improved self-care behavior with use of telemonitoring. There is insufficient and conflicting evidence to determine how long the effectiveness lasts. Medium- to high-quality studies, low to mod risk of bias |
Maddison et al. [87] | RCT non-inferiority trial | Heart disease (n = 162) | Remote telerehabilitation with monitoring Intervention: telerehabilitation exercise prescription, exercise monitoring (vitals, ECG, and accelerometry), coaching, and theory-based behavioral strategies. Control: Clinic-based in-session monitoring. Three sessions/week for 12 weeks. Ranged from 30 to 60 min sessions and 40%–65% heart rate reserve | Effect: Remote telerehabilitation program with monitoring was non-inferior to clinic-based rehabilitation program. Remotely monitored participants were significantly less sedentary compared to the control. Clinic-based participants had better improvements in waist and hip sizes compared to intervention. No other between-group differences were detected in VO2max, exercise adherence, motivation, or quality of life. Costs: The per capita program delivery and medication costs were significantly lower for the remote monitoring group. The hospital service utilization costs were not statistically significantly different between groups. |
5. Obstacles, Implementation, and Suggestions
5.1. Obstacles
5.1.1. Patient/Clinician Needs: Lack of Research on Usability and Patient Centered Outcomes
5.1.2. Effectiveness: Difficulty with Comparisons, Insufficient Research across Populations, Lack of Long-Term Outcomes
5.1.3. Lack of Healthcare Service Outcomes
5.1.4. Lack of Implementation Outcomes and Strategies
5.2. Implementation and Suggestions: A Path to Facilitated Adoptions through Hybrid Research
6. Discussion
6.1. Summary of Findings and Comparison to Other Studies
6.2. Contributions
6.3. Limitations and Conclusions
Supplementary Materials
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
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Author | Study Design | Population | Intervention | Outcome |
---|---|---|---|---|
neurological (stroke, parkinson’s disease, vestibular disorders) | ||||
Chu et al. [58] | Systematic review and meta-analysis | Vestibular disorders (n = 20 studies, 968 subjects) | VR Mixed home and supervised sessions 4–45 min sessions, 1–6 days/week, 3–12 weeks | Improved Dizziness Handicap Inventory [SMD]: −7.09, 95% CI: [−2.17, −2.00]); no effect on Activities-Specific Balance Confidence scale High heterogeneity |
Heffernan et al. [59] | Systematic review and meta-analysis | Vestibular Dysfunction (n = 5 studies, 204 subjects) | VR and AR 20–45 min, 4–6 weeks | Dizziness Handicap Inventory SMD 1.13 (95% CI, −1.74, −0.52); high risk of bias noted |
Mohamed Hazza et al. [60] | Systematic review and meta-analysis | Vestibular dysfunction (n = 6 studies, 258 subjects) | VR 10–45 min, 2–7 days/week, 1–6 weeks | Balance MD −3.27 (95% CI −4.27, −1.84); Dizziness VAS MD 25.13 95% CI (12.96, 37.29); Dizziness Handicap Inventory MD −12.93, 95% CI (−24.18, −1.69); No effect Activities-Specific Balance Confidence or Vertigo Analogue Scale |
Demeco et al. [11] | Systematic review | Stroke (n = 12 studies; 350 subjects) | VR 30–120 min, 2–5x/week, 2–9 weeks | Improved upper limb function, gait, and balance. High heterogeneity. |
Gil et al. [70] | Systematic review and meta-analysis | Stroke and older adults (n = 11 studies, 4 studies for meta-analysis, 308 subjects) | AR 20–120 min, 1–5x/week, 1–12 weeks | No effect balance (−1.12 (95% CI −3.54, 1.31), small effect on function (Timed up and Go) 92.81 (95% CI 1.04, 4.58) |
Sevcenko et al. [10] | Systematic review | Stroke (n = 10 studies) Parkinson’s disease (n = 8 studies), 1052 subjects | VR 2–7x/week, 2–6 weeks | May be as effective as conventional treatments and may be more motivating. Good to high study quality |
Kwon et al. [12] | Systematic review and meta-analysis | Parkinson’s disease (n = 14 studies, 524 subjects) | VR 30–60 min, 2–5 days/week, 6–12 weeks | Improved balance (Berg Balance Scale (MD = 2.71 95% CI 1.45–3.96) and Balance Confidence scale (MD = 9.43, 95% CI 5.67–13.19)); no improvement in gait, ADLs, motor function, or quality of life; risk of bias low to high; heterogeneity low to moderate |
Musculoskeletal | ||||
Blasco et al. [61] | Systematic review | Total knee replacement rehabilitation (n = 6 studies; 312 subjects) | VR with rehabilitation 20–60 min, two to seven sessions/week, 6–48 weeks | Improved balance; no improvement on function, pain, or satisfaction |
Choi et al. [62] | Systematic review and meta-analysis | LBP (n = 11 studies, 1761 subjects) | Virtual-reality-based rehabilitation Intervention details not identified | Pain: small to medium effect (SMD = +/− 0.37, 95% CI (0.75 to 0.00) Low bias, high heterogeneity |
Youssef et al. [63] | Systematic review | Orthopedic patient subjects (n = 19 studies, multiconditions, findings for arthritis and pain reported) | VR 45–60 min, 2–3 days/week, 6–12 weeks, | No difference compared to conventional care for knee osteoarthritis and neck pain; inconclusive for low back pain |
Guo et al. [64] | Systematic review and meta-analysis | Neck pain (n = 8 studies, 382 subjects) | VR 20–360 min, 1–6 weeks, 1–4 weeks | Small effect pain intensity (SMD −0.51, 95% CI −0.91, −0.11); improved disability, kinesiophobia, and range of motion in VR group. High heterogeneity, limited quality; adverse event motion sickness |
Ye et al. [65] | Systematic review and meta-analysis | Neck pain (n = 5 studies, 192 subjects) | VR | Modest improvement in pain (VAS SMD—0.58 (95% CI (−0.91—0.25) Neck Disability Index (SMD = −0.54; 95% CI (−1.24, 0.15); ROM non-significant difference |
Diabetes | ||||
Lee [71] | Randomized control trial | Diabetes (n = 45 subjects) | VR Three-arm study: (1) Control group: typical routine (2) IG: VR (3) IG: Exercise 40–60 min, 3x/week, 2 weeks | VR and exercise group improved mean blood glucose (F = 12.001 p < 0.001) and serum fructosamine (F = 3.274, p = 0.016) compared to the control group. Both intervention groups had significant improvement in muscle mass compared with the control group (F = 4.445, p = 0.003). No difference in body mass index. |
Pulmonary disease | ||||
Rutkowski et al. [72] | Randomized control trial | COPD (n = 106) | Three groups: (1) endurance training pulmonary rehab (ET); (2) pulmonary rehab + VR and endurance training (ET + VR); (3) pulmonary rehab + VR (VR) Endurance exercise: 20–30 min VR: 20 min Pulmonary rehab components 5 days/week X 2 weeks | ET + VR group superior to ET group in arm curl (p < 0.003), chair stand (p < 0.008), back scratch (p < 0.002), chair sit and reach (p < 0.001), up and go (p < 0.000), and 6-min walk test (p < 0.011). VR group was superior to ET group in arm curl (p < 0.000), chair stand (p < 0.001), and 6-min walk test (p < 0.031). |
Heart Disease | ||||
Bouraghi [68] | Systematic review | Cardiac disease (n = 26 studies, 1281 subjects) | VR: rehabilitation 2–3x/week, 2 weeks–6 months | Reduced pain and length of hospitalization and improved systolic blood pressure and heart rate. |
García-Bravo et al. [67] | Systematic review | Cardiac rehabilitation (n = 10 studies, 874 subjects) | VR and Video Games + cardiac rehabilitation 20–60 min, 2–7 sessions/week, 6 weeks–12 months | Increased heart rate, less pain, a greater ability to walk, higher energy levels, an increase in physical activity, and improvements of motivation and adherence |
Blasco-Peris et al. [66] | Systematic review and meta-analysis | Cardiovascular disease in cardiac rehabilitation (n = 8 studies, 733 subjects) | Exergaming component to cardiac rehabilitation compared to traditional cardiac rehabilitation 20–60 min, 2 sessions/day–7 sessions/week, 6–48 weeks | Non-significant statistical difference between exergaming and conventional cardiac rehab programs in exercise capacity changes (measured as the distance covered in the 6MWT). |
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LaMarca, A.; Tse, I.; Keysor, J. Rehabilitation Technologies for Chronic Conditions: Will We Sink or Swim? Healthcare 2023, 11, 2751. https://doi.org/10.3390/healthcare11202751
LaMarca A, Tse I, Keysor J. Rehabilitation Technologies for Chronic Conditions: Will We Sink or Swim? Healthcare. 2023; 11(20):2751. https://doi.org/10.3390/healthcare11202751
Chicago/Turabian StyleLaMarca, Amber, Ivy Tse, and Julie Keysor. 2023. "Rehabilitation Technologies for Chronic Conditions: Will We Sink or Swim?" Healthcare 11, no. 20: 2751. https://doi.org/10.3390/healthcare11202751
APA StyleLaMarca, A., Tse, I., & Keysor, J. (2023). Rehabilitation Technologies for Chronic Conditions: Will We Sink or Swim? Healthcare, 11(20), 2751. https://doi.org/10.3390/healthcare11202751