Posts Tagged compliance

[ORIGINAL REPORT] View of Compliance with Upper Limb Home-Based Exergaming Interventions for Stroke Patients: A Narrative Review

Background: Telerehabilitation and follow-up techniques have been developed in recent years to assess the effectiveness of diverse intervention programmes that include exergaming technologies. For patients with upper limb impairment after stroke, motion-gaming technologies can provide effective and amusing training. Beyond efficiency, professionals must analyse patient compliance with the system for self-use at home, because patients may or may not independently perform the exercises prescribed by the therapist. Questions on the sustainable use of this type of home exercise also arise.

Objective: This review examines user compliance with exercise programmes, measured according to the training rate (percentage of prescribed sessions and minutes completed) and completion rate (number of drop-outs and discontinued interventions) reported or calculable according to the data collected.

Results and discussion: Rates of compliance with training were relatively high. No group effect on compliance was found. Drop-out and discontinued intervention rates were either due to external causes or directly related to the technologies. Some studies have reported the use of supervision, most of them through home visits and remote support. Few studies performed long-term follow-up, which could provide information to help broaden practices. This narrative review considers how this field of research may evolve in the future.

LAY ABSTRACT

The use of video games in hospitals as a rehabilitation tool in neurology is developing, particularly for stroke victims. For patients with arm problems, it can be effective and fun to use gamified systems. When the patient goes home, they must continue their rehabilitation in order to continue to progress or maintain their skills. However, performing exercises alone at home raises questions about patients’ compliance with the exercises prescribed by their therapists. Do patients complete the prescribed sessions? Are there occasional or permanent interruptions? This narrative review attempts to address these questions. The review also examines the obstacles that might hinder the use of these technologies and the facilitators that may help compliance.

Telerehabilitation offers an alternative rehabilitation technique through the delivery of rehabilitation and habilitation services via information and communication technologies (ICTs) (12). Telerehabilitation is a useful approach in outpatient rehabilitation, especially for post-stroke patients (3). Stroke was the second-leading cause of death and third-leading cause of death and disability combined worldwide in 2019 (4). Stroke is highly prevalent among older patients, many of whom have underlying health issues (e.g. diabetes, hypertension, and cardiovascular disease). Upper extremity paralysis is a predominant impairment after stroke, with a recovery rate of 10–20% (5), affecting independence and quality of life (6). This reflects the importance of post-hospital discharge support programmes. Telerehabilitation is one possible approach in outpatient stroke rehabilitation, with follow-up at home.

Exergaming, otherwise known as exercise-based games (e.g. virtual reality and interactive video-game interventions) is a relevant alternative home-based rehabilitation for persons with neurological diseases. The effectiveness of these interventions has been shown to be at least equivalent to conventional therapy or usual care (7). Most studies have focused on assessing the effectiveness of the technologies, but patient compliance with these technologies is under-explored. Even if the technology can be adapted technically or physiologically, it remains necessary for the patient to want to use it; therefore, effective implementation for self-use at home depends on patient compliance.

Medical compliance was defined in the late 1970s as “the extent to which the patient’s behavior in terms of taking medications, following diets, or executing other lifestyle changes coincides with medical or health advice” (8). Exercise compliance is defined as “a person’s compliance with a prescribed or self-prescribed fitness program” (9). The terms compliance, adherence, and concordance are often used interchangeably (10). The term compliance is used throughout this narrative review as an indication of positive patient behaviour in following an exercise programme. Many people do not feel motivated to engage in new habits, including exercise. In 2013, a meta-analysis showed that approximately 21% of people did not intend to take up physical activity, while 36% intended to, but found changing their sedentary behaviour difficult (11). Training is often limited by a lack of motivation, which can be the main reported reason for non-adherence with home exercise by individuals with chronic stroke (12). Designing optimal rehabilitation treatment programmes for stroke patients requires an understanding of “What” is the content of the treatment, “How much” treatment is required, and “When” treatment is best delivered (13).

This narrative review assesses patient compliance according to the type of upper limb technology used and the home implementation parameters.

GAME-BASED SYSTEMS IN THE HOME-BASED SETTING

Exergaming is defined as the integration of physical activity into a video-game environment that requires active body movements to control the game (14). The emergence of commercial video-game systems, coupled with handheld controllers and motion-capture devices, has facilitated the use of computer games for neurorehabilitation. These technologies have the potential to be effective for increasing upper limb capacities (1518). Game-based systems may offer a motivational exercise environment that encourages continued use. Health professionals and participants have reported high levels of satisfaction and acceptance of telerehabilitation interventions (5). Piron et al. (2008) showed that post-stroke patients with arm motor impairments assigned to the home-based virtual reality group were able to engage in therapy at home through a user-friendly system, and the videoconferencing system ensured a good relationship between the patient and the remote therapist (19). Their study was based on the patient’s degree of satisfaction, an important indicator of the efficacy of the therapeutic intervention, which improves the patient’s motivation to engage in rehabilitation.

A range of commercial gaming systems are described in the literature for home use: Kinect™ (Microsoft Corporation; Redmond WA, USA) (30323443), Wii™ (Nintendo, Japon) (2528), Vive™ (HTC, Taïwan) (29), PlayStation® 3 Eye Move controller (Sony, Japon) (26), Leap Motion controller (Ultraleap, USA) (30) (Table I). These devices are mostly associated with custom games and other specific rehabilitation devices, such as robotic devices, specific controllers, and passive arm support (e.g. TheraBot system (Rehabilitation Robotics and Research and Design Lab, Milwaukee, WI, USA) (31), SaeboMAS (Saebo Inc., Charlotte NC, USA) with SCRIPT dynamic wrist and hand orthosis sensor (32), HandinMind (HiM) system (33) (Hocoma AG, Switzerland), P5 Glove (Essential Reality Inc; NY, USA) (24), Armeo®Senso (Hocoma AG, Switzerland) (34), BrightBrainer™ Grasp (Bright Cloud International, NJ, USA) (29), Myo Band (n.a) (26), MusicGlove (FlintRehab, CA, USA) (35), CyWee Z controller (CyWee Inc., Taiwan) (36) and passive arm support (30)) (Table I).

Author, yearDesign Methods Data collectionParticipantsTechnologyImplementation parameters (number of sessions, frequency, and length)Home training (min)Drop outDiscontinued intervention
Brokaw et al. (43)Pilot evaluation of the usability and utility in the home Qualitative Interview1 stroke patientComputer screen, Kinect™ (Microsoft Corporation; Redmond WA, USA), 5 custom games19 sessions 30 min, 5 days/week, for 4 weeksNRNo1 session hardware not used final 3 training sessions
Burdea et al. (29)Feasibility study Mixed Survey + training7 chronic post-stroke patients 7 caregiversBrightBrainer™ (Bright Cloud International, NJ, USA) computer, Vive™ (HTC, Taïwan) and BrightBrainer Grasp controllers, custom games, Automatic electrical meter20 sessions wk 1 20 min wk 2 25 min wk 3 30 min wk 4 40 min 5 days/week, 4 weeks605 min1 screening failure (low MOCA score)NR
Chen et al. (26)Qualitative study in a randomized trial Qualitative semi-structured interviews13 stroke patientsComputer, Myo Band, Wiimote™ (Nintendo, Japon) in a pistol-shaped holder, Power Mate, PlayStation® 3 Eye Move controller (Sony, Japon), Joystick, Logitech Trackpad, real-time video guidance36 sessions 70 min at a fixed time every day 6 days per week, over 6–8 weeksNRNoNR
Dodakian et al. (35)Pilot study Quantitative Survey12 stroke patientsLaptop, wrist accelerometer sensor, MusicGlove (FlintRehab, CA, USA), 18 games, videoconference1 structured hour + 1 h of free play, for 28 days (2 × 14-day separated by a 1–3-week break)Active time (games+exercises): 60 ± 10 min/d, including a mean of 22 ± 24 min/d of free play. Total time (active time + education questions, measuring blood pressure, reading game instructions, donning devices, and taking breaks between tasks): 182 ± 61 min/d.No1 not completed 4 sessions (fatigue) 1 not completed 1 session (hardware malfunction) 1 missed 2 complete sessions (other medical appointments)
Fluet et al. (30)A Feasibility and pilot study – comparison Mixed Survey + training11 stroke patients: 5 enhanced motivation (EM) group + 6 unenhanced control (UC) groupLeap Motion controller (Ultraleap, USA) passive arm support, custom-designed simulationsAs much as possible, but at least 20 min, daily for 12 weeks> 400 sessions. Enhanced motivation group: 95±95 min per week (range 40–276 min) Unenhanced control group: 35 ± 31 min per week (range 3–93min)NRNR
King et al. (36)Case series (after a trial of 10 sessions of bilateral therapy using VR) (Hijmans et al.2011) Mixed Survey + Training3 patients with chronic strokeComputer screen, CyWee Z controller (CyWee Inc., Taiwan) gamesChose when and for how long for in each session, for no longer than 90 min on any given day Each game at least once, after free to choose the proportion of time on any games for 8 weeks≥ 35 min per session ≥ 4.5 times per week ≥ 33.5 hcontinued for between 55 and 61 days at homeNoDiary: mean number total of days missed: 11.66
McNulty et al. (25)a randomized controlled trial Mixed Survey + structured interview + training41 stroke patients (21 + 20)Wiimote™ (Nintendo, Japon) Wii Sports™ games10 sessions 60 min weekdays, progressively increasing, for 14 days follow-up 6 monthsWii-based Movement Therapy (WMT): 1,188 min modified constraint-induced movement therapy (mCIMT): 1,194 min. Completion rates 105.7 (93.6–114.7)% (WMT) and 101.0 (87.6–108.1)% (mCIMT)2 EG (withdrew+death) 1 CG (unrelated medical condition)NR
Nijenhuis et al. (32)Pilot randomized controlled trial Mixed Survey + semi-structured interview + training20 stroke patients (10 + 10)Computer, SaeboMAS (Saebo Inc., Charlotte NC, USA) SCRIPT dynamic wrist and hand orthosis sensor, games36 sessions at least 30 min per day, 6 days a week, for 6 weeks follow-up 2 monthsCG: 189 (143–266) min per week EG: 118 (51–176) min per week ranging from 13 to 423 min per week1 EG (shoulder pain due to external causes)NR
Sivan et al (49)Feasibility study Qualitative semi-structured interview17 (9 prototype) patients + 7 therapistsComputer screen, powered joystick, controlled assistance, 8 games8 weeksNRNRNR
Standen et al. (27)Prospective cohort study plus qualitative analysis Mixed Semi-structured interview + training29 stroke patients, including 17 in the qualitative studyPC, Virtual glove, Wiimote™ (Nintendo, Japon), 3 custom games3 times a day for periods of no more than 20 min, for 8 weeksPercentage of the duration of use ranged from 1.46 to 70.6 percentage of days used ranged from 10% to 100%Allocation: 4 EG (family issues, not interested, arm pain, severe aphasia) Follow-up: 1 CG (measures onerous) + 3 EG (illness, ill family member, going on holiday)NR
Thielbar et al. (21)Randomized trial – crossover, interventional study Mixed Survey + Training20 chronic post-stroke patients (10 in the FSU group and 10 in the FMU group)Computer, Kinect™ Microsoft Corporation; Redmond WA, USA) wireless mouse. 3 custom exercises, voice communication, remote central server, custom Google Cloud Virtual Machine8 sessions 4 sessions of 1 h each week, for 4 weeks: 2 weeks with multi-user (MU) + 2 single-user (SU) versionFor the SU mode, FSU group: 30.2 ± 10.8 min and FMU: 39.9 ± 12.8 min For the MU mode, the FSU and FMU groups had similar times1 (medical reasons) 1 FMU group (declined participation)MU mode: 18 of 20 subjects participated in all 8 sessions, and all 20 subjects participated in at least 7 sessions SU mode: only 15 of 20 subjects participated in all 8 sessions, and 16 of 20 participated in at least 7 sessions
Wingham et al. (28)Pragmatic multi-centre RCT with a qualitative study and health economics analysis Qualitative semi-structured interview19 stroke patients 10 caregiversTelevision, Wii console, Wii gamesFor up to 45 min daily for 6 weeks followed up at 6 weeks and 6 monthsEG: 37 min (range 4–108 min) CG: 32 min (range 4–63 min)1 (timetable)NR
Wittmann et al. (34)Feasibility study Mixed Structured patient interview + training11 stroke patientsArmeo®Senso (Hocoma, Switzerland) = wearable inertial measurement units (IMU)As often as possible for 6 weeks26.5 ± 11.5 (min 8, max 41) days out of 42 days duration per week: 137 ± 120 min (min 15, max 357) training sessions on 4.4 days per week training (gaming) duration per session: 30 ± 16 min (min 11, max 56)NRNR
NR: non-recorded; EG: experimental group; CG: control group; EM: enhanced motivation group; UC: unenhanced control group; WMT: Wii-based movement therapy; mCIMT: modified constraint-induced movement therapy; SU: single user; MU: multi-user, wk: weeks; min: minimum; max: maximum; MoCA: montreal cognitive assessment.

Some studies included real-time audio or video systems (3031394347). The exergames used in the studies were specific or non-specific systems for upper-limb stroke rehabilitation. Devices can be used alone or in combination with other technologies (e.g. exoskeleton, robotics, exogenous stimulation, virtual reality headsets, and augmented reality), potentially further improving recovery. It is of interest to determine whether combinations can have a positive impact on compliance. For example, in the REINVENT platform (37), researchers combined the principles of action observation in head-mounted virtual reality with brain-computer interface (BCI) neurofeedback for stroke rehabilitation to try to elicit optimal rehabilitation gains. It would be of interest to assess the relevance of this on functional activities and in different settings (e.g. laboratory, clinic, home). As reported by Perrochon et al. (2019), future studies in the home should include the multiple observations reported in the literature to ensure an optimal exergaming design (738).

HOME EXERCISE REGIMEN

Several systematic reviews have indicated that intensive treatment is favoured, but there is no consensus on the optimum amount, intensity, distribution, or duration of therapy (39). Across a large number of studies, the key elements of task-specific training are repeated, challenging the practice of functional, goal-oriented activities (4042). Motion-tracking systems provide real-time feedback regarding execution of task-specific exercises, but it is unclear which is the most efficient training. To our knowledge, there are no guidelines regarding the appropriate maximum duration of research and clinical sessions to maintain compliance. Dose, frequency, and duration scheduling of home-based therapy are shown in Table I.

The overall dose ranged from 20 min (29) to 120 min per day (1 h structured activity and 1 h free play) (35). The recommended time increased stepwise each week for 1 study (29), whereas another progressively increased the time over 10 consecutive weekdays (25). Three studies did not give the number of expected min per day (303436). Three studies indicated a time limit not to be exceeded; users played for as long as they wanted in a session and whenever they wanted, but for no longer than 90 min on any given day (36); 3 times per day for periods of no more than 20 min (27); or for up to 45 min daily (28). Conversely, another study indicated a minimum time limit requirement of 20 min daily (30). Time of day can be defined to accommodate the necessary appointments with therapists (2126). The current review observed variability in the prescriptions: studies proposing 30 min per day were considered as sub-therapeutic. In contrast, planning 1–2 h per day of task time and assessing repetitions and intensity accurately were recommended (13).

The number of sessions ranged from 8 (21) to 36 (2632). Six studies did not specify the number of expected sessions ((2728303436). The number of days per week were set at 5 (2943), 6 (2632) or 7 (2835). Hence, the sessions were discontinuous or continuous, depending on the study.

The most often used training duration in the studies was 6 weeks (2628323436). Other studies had a total intervention duration ranging from 14 days (25) to 12 weeks (30). Only 1 study planned an interruption after 14 days of 1–3 weeks halfway through the intervention (35). They explained that 14 days was selected based on the success of the EXCITE trial of constraint-induced therapy, which showed benefits when making daily demands on patients for 14 days (44). Only 3 studies proposed follow-up to assess the persistence of improvements in motor function. They did not indicate any information on long-term engagement.

COMPLIANCE ASSESSMENT

Training compliance rate

Some authors referred to the training rate to assess compliance quantitatively. The ratio of the quantity of training performed by the patient to the quantity prescribed by the therapist was reported or calculated. Some authors considered the total training time, in minutes, performed by the study subject, the mean number of sessions per week, and the mean minutes per session for home-based interventions. These data can be compared with the authors’ recommendations.

Certain studies calculated high compliance rate of approximately 96% (29). Other authors compared groups, for example, compliance was very high (99%) for the multi-user mode and 89% for the simple-user mode, suggesting that the training mode can affect the compliance (21). More, the change in the difficulty and complexity showed a greater increase in training time per session than the control group (30). Some other studies have a compliance rate of over 100, taking 100% as the time prescribed by the therapist. Indeed, some studies allow patients to do more exercises if they wish following their prescribed time (3032). For example, the completion rate was 105.7% (93.6–114.7%) for the Wii-based movement therapy and 101.0% (87.6–108.1%) for the control group (median, interquartile range) (25). Conversely, a high compliance rate was found for the control group (105%), but not for the experimental group using computerized gaming exercises (65.6%) (32).

A few studies reported the number of repetitions performed during the intervention (293435). However, with few comparative data, we chose not to report the data in this review.

Participants in the study by Nijenhuis et al. (32) recorded the frequency and duration of training in a diary to assess user compliance with training duration and motivation. King et al. (36) used the same methods to assess patient engagement quantitatively, using diaries to record the occurrence and duration of the intervention.

Attrition rate

The attrition rate is calculated as the number of drop-outs and discontinued interventions. Within eHealth interventions, the exponential decrease in adherence has been described as the “Law of Attrition” (45). It is essential to consider the main causes of the rate and to set up tools to reduce the level of attrition as much as possible. Dropping out of therapy is an implicit marker of dissatisfaction or unacceptability. Variability in acceptable discontinued intervention/drop-out rates was found in the literature, ranging from 5%, to 20%, and 30% for follow-up of more than 1 year (46).

Literature results showed a high attrition rate for the home-based setting, although the drop-out rate was higher for the experimental group than for the control group (252732). The completion rate was not described in all studies. However, among the studies that evaluated the completion rate, variable results were found. For example, a 94.7% rate for intervention completion was reported by Brokaw et al. (43), with only 1 missed session and a 97.9% rate was described by Dodakian et al. (35) with 3 patients not completing or missing sessions. King et al. (36) provided the number of days of intervention over the total intervention period for each subject, recorded by the participants in diaries, and reported a rate of 79.9%. Thielbar et al. (21) compared the training attrition rate between groups: in the multi-user (MU) mode, 90% of subjects participated in all 8 sessions, and 100% participated in at least 7 sessions. However, in the single-user (SU) mode, only 75% of subjects participated in all 8 sessions and 80% participated in at least 7 sessions (21).

BARRIERS TO COMPLIANCE

Non-compliance was intentional or non-intentional. Some factors were due to internal factors (no interest, pain, fatigue, severe aphasia, seizure, illness, death, etc.) and others to external factors (family issues, ill family member, holidays, schedule). This led to limited compliance, and patients either dropped out or discontinued the interventions. Some non-compliance factors were correlated with technical issues: Brokaw et al. (43) reported that participants completed 18 of the planned 19 sessions, but hardware issues prevented participants from using the system for the final 3 training sessions; Some studies reported technical issues with the hardware (2629354349), the software (35), communication reliability causing storage data problems (29), the home setting (262949), unsuitability for use with spastic hands (29), and time constraints (26). These aspects did not necessarily stop the patients from participating in the study. As reported by Perrochon et al. (2019), the rate of drop-out and discontinued interventions were due either to external causes or directly related to the technologies (7). Dodakian et al. (35) produced a summary document of the issues, solutions, and lessons learned for future telerehabilitation studies. This initiative is relevant for future perspectives. As Ong et al. (2018) stated, identifying manipulable aspects of treatment that reduce the probability of drop-out can guide the development of more acceptable interventions (47).

FACILITATORS OF COMPLIANCE

Some authors proposed a familiarization stage with the device before home use. Some studies provided laboratory familiarization before home use: 1 session (43), a brief 2- or 3-day orientation (21), and 10 sessions (36). Familiarization directly at home was also prescribed: 1 session (29) and 2 sessions (43). Other studies established an initial visit for training purposes (2730). These sessions equipped participants with the skills to continue the programme safely and independently at home.

Other means were established to carry out the intervention. One study supplied an instruction manual at the beginning (frequently asked questions and tips) (27), whereas another used a transfer package in each session including different forms to emphasize patient safety, monitor home practice, improve handling and compliance, and provide a forum for patient-centred goal-setting and problem-solving (25). This allows for self-care before calling in the therapists.

However, remote assistance was necessary in most of the studies for which it was made available. Technical issues were expected during studies with this type of technology. Some systems can be used as remotely monitored telerehabilitation; for example, some studies used only telephone calls while others used videoconferencing, education videos, web-based chats, or virtual reality systems (48). Clinicians can propose appropriate responses by adapting and personalizing the planned rehabilitation activities and offering technical assistance when needed. It is important to verify whether the use of telerehabilitation systems can improve patient engagement by conducting their rehabilitation training at home in a safe environment.

Four studies supervised the interventions by combining home visits and remote support via phone calls (27293043), whereas 1 study relied only on home visits (32). Two studies used videoconferencing and remote support (2635) and 1 study scheduled remote appointments using the remote therapist-patient systems and telephone support (21). Remote access to data on participants’ playing performance can be used to verify compliance with the protocol (29). It can be a way to automatically inform the researcher if the data has not been uploaded for three consecutive days (29). The first home visits included a time dedicated to installation and explanations with patients and possibly caregivers. Some studies did not offer supervision (343649).

Furthermore, some authors requested patient feedback. Participants in the study by Chen et al. (26) specified having received support following minor technical issues. Participants and caregivers in the study by Wingham et al. (28) said they felt reassured and supported by the weekly phone call, but also appreciated the social connection.

Dodakian et al. (35) measured the assistance given by phone during the study. The authors supposed that the decrease in assistance required over time might be due to patient familiarity with the system and improved performance of the study team.

Videoconferencing allowed therapists to observe patient performance, answer questions, review the treatment plan, and, on select days, perform brief study assessments (26). In the same study, daily 30-min half-therapy sessions were supervised by videoconference, followed by 40 min during which the patient was alone. Dodakian et al. (2017) proposed 3 videoconferences per week, focusing on the prior week’s activities, followed by a structured interview including specific inquiries on pain, adverse events, and the telerehabilitation system performance. The authors explained that providing feedback and encouragement could increase motivation, according to the standard of care (35). Johnson et al. (2011) described simple encouragement provided through video and audio feedback via a robot assistant (31). In addition to the aspects of communication with the user and monitoring of progress, it could also allow for remote monitoring of the the user’s position when using the device (49).

Fluet et al. (30) described modest motivational enhancements and discussed areas for increasing the training time per session. One suggestion was that supervision in the form of email and text message reminders of weekly tasks could increase the number of training sessions.

It is important to make the games interesting and stimulating to increase the use of the device (49). Integration of the multi-player mode within a game-based task could also be a factor in increasing compliance (2149).

DISCUSSION

Compliance behaviour is complex, requiring an analysis based on theoretical models. Over the years, specific theoretical models for studying compliance have been described. In the Health Belief Model (HBM), compliance is determined by the knowledge and attitudes of the patient (50). There are 4 essential areas in the development of compliant behaviour: perceived susceptibility; perceived severity; perceived benefits; and perceived barriers. More recent forms of the HBM emphasized 2 other factors in the decision to engage in a behaviour: (i) self-efficacy, which is the patient’s belief that he or she is capable of taking the recommended action; and (ii) action cues, which are aids that teach or remind the patient of the recommended action (51). Designing a novel technology for stroke patients involves a deep understanding of the persons who use the system and perform the activity, and the context in which that activity takes place. User expectations and needs must be understood, as must their motivations, and previous experiences (52). The context of use is also a key element to explore at this pre-implementation stage and to evaluate at the post-implementation stage. The architectural, material, and human environment must be considered with regard to use of the system in the patient’s home. Evaluating user experience with interactions and the use of the system is relevant to obtain patient reactions in post-task interview questions (53), and in particular, in terms of compliance with use and engagement.

Most researchers used an off-the-shelf system (i.e. a commercial system) as a primary tool and combined it with elements or games adapted to neuro-rehabilitation. According to Tamayo-Serrano et al. (2018), low-cost solutions are expected to promote the adoption of in-home rehabilitation systems by patients and health organizations (54). To be able to assess cost-effectiveness, quantified cost and time data must be considered. For example, Lloréns et al. (55) reported the cost of telerehabilitation and in-clinic programmes. Costs were reported in terms of human resources (time spent on assistance and guidance during the intervention, progress monitoring, and troubleshooting), round trips to the neurorehabilitation unit, and instrumentation (laptop, Kinect™, and internet access) (55). The cost of the clinical instrumentation was not considered, but this would have provided additional information for comparison. More transparency on the costs incurred would be useful for future studies. Table II summarizes the current literature on compliance.

TopicsDefinitionsMajor findings
Game-based systems in home settingsExergaming: the integration of physical activity into a video game environment that requires active body movements to control the gameMost researchers used an off-the-shelf system (i.e. commercial system) as a primary tool with added elements or games adapted to neuro-rehabilitation
Home exercise regimenAmount, intensity, distribution, or duration of treatment recommended by therapistsVariability in current prescriptions.
30 min per day is considered sub-therapeutic. Recommended to plan 1–2 h per day of task time and to assess repetitions and intensity accurately
Training compliance rateRatio between quantity of training completed by the patient and quantity previously prescribed by the therapistPatients generally follow the prescription and some even go further by continuing to train if allowed. There is no group effect on compliance (it may be greater for the experimental group than the control group, or vice versa)
Attrition rateDrop-out: percentage of subjects failing to complete a study
Discontinued intervention: percentage of sessions failing to complete
High attrition rate for the home-based setting, although the drop-out rate was higher for the experimental group than for the control group
The rate of discontinuation of intervention is lower for the multi-user (MU) mode than the single-user (SU) mode
Compliance barriersCauses of non-complianceInternal factors: no interest, pain, fatigue, severe aphasia, seizure, illness, death
External factors: family issues, ill family member, holidays, timetable
Technical adverse events: hardware, software, communication reliability causing storage data problems, home environment, unsuitability to use with spastic hands, time constraints
Compliance facilitatorsOptions for promoting exercise complianceExplanations given by the therapist before the intervention
Familiarization stage
Notices/instructions available
Remote or in-person assistance
Remote or in-person monitoring
Forum for patient-centred goal-setting and problem-solving
Logbooks and diaries
Multi-player mode

CONCLUSION AND PERSPECTIVES

This narrative review identified current practices for user involvement in the development of stroke-patient decisions on home-based gaming technology. This review studied compliance with technologies adapted to post-stroke rehabilitation. The literature on the subject is recent. Heterogeneity is found on the type of technologies, the intervention regime, and the supervision, making it difficult to draw conclusions on compliance. More robust studies are needed to provide additional data.

In general, home-based gaming therapies are well received by patients and no significant problems occur. Additional experimental studies are required to understand which determinants, intrinsic to devices, impact the user’s compliance. Further research into the conditions for the personalized specification of the technological devices, developed in co-construction with the user, would be useful. Current studies focus on short-term evaluations; however, a long-term view is necessary to assess user compliance for high-ecological validity. Future studies should investigate how emerging technologies enable long-term use and the transfer of the acquired knowledge to everyday life, and should identify resources and assess the suitability of the system’s settings based on the best situation for home use.

ACKNOWLEDGEMENTS

The authors thank Hugo Landais and “La Fondation de l’Avenir pour la recherche médicale appliquée” (Paris, France) and the European Institute of Technology (EIT Health) for their scientific insights and unyielding support.

Authors’ declaration of authorship contribution

All those designated as authors meet the International Committee of Medical Journal Editors (ICMJE) requirements for authorship.

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[ARTICLE] Adherence to Guidelines in Adult Patients with Traumatic Brain Injury: A Living Systematic Review – Full Text

Abstract

Guidelines aim to improve the quality of medical care and reduce treatment variation. The extent to which guidelines are adhered to in the field of traumatic brain injury (TBI) is unknown. The objectives of this systematic review were to (1) quantify adherence to guidelines in adult patients with TBI, (2) examine factors influencing adherence, and (3) study associations of adherence to clinical guidelines and outcome. We searched EMBASE, MEDLINE, Cochrane Central, PubMed, Web of Science, PsycINFO, SCOPUS, CINAHL, and grey literature in October 2014. We included studies of evidence-based (inter)national guidelines that examined the acute treatment of adult patients with TBI. Methodological quality was assessed using the Research Triangle Institute item bank and Quality in Prognostic Studies Risk of Bias Assessment Instrument. Twenty-two retrospective and prospective observational cohort studies, reported in 25 publications, were included, describing adherence to 13 guideline recommendations. Guideline adherence varied considerably between studies (range 18–100%) and was higher in guideline recommendations based on strong evidence compared with those based on lower evidence, and lower in recommendations of relatively more invasive procedures such as craniotomy. A number of patient-related factors, including age, Glasgow Coma Scale, and intracranial pathology, were associated with greater guideline adherence. Guideline adherence to Brain Trauma Foundation guidelines seemed to be associated with lower mortality. Guideline adherence in TBI is suboptimal, and wide variation exists between studies. Guideline adherence may be improved through the development of strong evidence for guidelines. Further research specifying hospital and management characteristics that explain variation in guideline adherence is warranted.

Introduction

Traumatic brain injury (TBI) is a major public health concern affecting approximately 150–300 per 100,000 persons annually in Europe.1 The World Health Organization has predicted that TBI will be one of the leading causes of death and disability worldwide by the year 2020.2

The care for patients with TBI is often complex and multidisciplinary. Guidelines, protocols, and care pathways have been developed to improve quality of care, to reduce variation in practice, and to ensure that evidence-based care is optimally implemented.3

A 2013 systematic review4 found that the use of protocols in the management of severe TBI in the intensive care unit (ICU) led to improved patient outcomes. The findings, however, were based on observational studies that did not report on adherence rates. Without an understanding of adherence rates, the improved outcomes stated in the review cannot be directly attributed to the use of protocols.

Guideline adherence can be defined as the proportion of patients treated according to a guideline recommendation, which often represents evidence-based or best practice care. Previous studies have found that guideline adherence in medicine is generally low5–7 and varies widely across centers,7,8 medical condition,9 types of guideline,10,11 and time period.8,10 As a result, many patients do not receive evidence-based care, while others receive unnecessary care that may even be harmful.5To date, no systematic review of the literature about guideline adherence in TBI has been conducted.

The aim of this systematic review was to provide a comprehensive overview of professionals’ adherence to guidelines in adult patients with TBI. The objectives were threefold:

  • 1. To quantify adherence to guidelines in adult patients with TBI.

  • 2. To explore factors influencing adherence to TBI guidelines in those studies reporting on adherence.

  • 3. To examine the association between adherence to guidelines and outcome in patients with TBI in those studies reporting on adherence.

Continue —> Adherence to Guidelines in Adult Patients with Traumatic Brain Injury: A Living Systematic Review | Journal of Neurotrauma

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[Abstract] Effectiveness of interventions to improve therapy adherence in people with upper limb conditions: A systematic review

Abstract

Study Design

Systematic review.

Introduction

Patient adherence to orthosis wear and/or prescribed exercises improves functional outcome after acute injury and can prevent deformities, contractures, and reinjury of tissues. This is the first systematic review to review the evidence of the effectiveness of interventions to improve treatment adherence in children and adults with acute or chronic upper limb injuries or conditions.

Purpose of the Study

The purpose of this study is to establish the effectiveness of interventions to improve hand therapy adherence in people with upper limb conditions and to report on outcome measures used when reporting adherence.

Methods

A literature search of MEDLINE (OVID), Embase (OVID), CENTRAL (OVID), CINAHL (EBSCO), and EmCare (OVID) (from inception to March 2017) was undertaken. Studies were selected if they met the following inclusion criteria: clinical trials; in adults or children with any injury or condition affecting the upper limb including acute trauma and injury; chronic and acquired musculoskeletal conditions; and neurological conditions. Two independent assessors rated the study quality and risk of bias using the Cochrane Collaboration tool for assessing the risk of bias.

Results

Eight studies met the inclusion criteria. Study quality ranged from 3 to 6 out of 7 points on the Cochrane risk of bias tool. There were 4 categories of intervention for improving adherence: orthosis/cast material/design; orthosis wear schedule; patient education mode for home exercise programs; and behavioral approaches. Due to heterogeneity of condition acuity, interventions, and outcomes reported, it was not possible to pool the results from all studies. Therefore, a narrative best evidence synthesis was undertaken. There is weak evidence from a very small number of trials that orthosis/cast material has no influence on treatment adherence in acute or chronic conditions and mode of patient education (audio-visual vs written) has no effect in acute conditions. There is low-to-moderate quality of evidence in support of behavioral interventions for achieving treatment adherence in chronic rheumatoid arthritis.

Conclusion

Behavioral approaches that encourage self-efficacy are likely to be useful in achieving treatment adherence in populations with chronic upper limb conditions. There is insufficient evidence for other interventions aimed at improving adherence in acute upper limb injuries and conditions.

via Effectiveness of interventions to improve therapy adherence in people with upper limb conditions: A systematic review – Journal of Hand Therapy

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[ARTICLE] 6-REXOS: Upper Limb Exoskeleton Robot with Improved pHRI – Full Text PDF

Abstract

Close interaction can be observed between an exoskeleton robot and its wearer. Therefore, appropriate physical human-robot interaction (pHRI) should be considered when designing an exoskeleton robot to provide safe and comfortable motion assistance. Different features have been used in recent studies to enhance the pHRI in upperlimb exoskeleton robots. However, less attention has been given to integrating kinematic redundancy into upper-limb exoskeleton robots to improve the pHRI.

In this context, this paper proposes a six-degrees-of-freedom (DoF) upperlimb exoskeleton robot (6-REXOS) for the motion assistance of physically weak individuals. The 6-REXOS uses a kinematically different structure to that of the human lower arm, where the exoskeleton robot is worn. The 6-REXOS has four active DoFs to generate the motion of the human lower arm. Furthermore, two flexible bellow couplings are attached to the wrist and elbow joints to generate two passive DoFs. These couplings not only allow translational motion in wrist and elbow joints but also a redundancy in the robot. Furthermore, the compliance of the flexible coupling contributes to avoiding misalignments between human and robot joint axes. The redundancy in the 6- REXOS is verified based on manipulability index, mini‐ mum singular value, condition number and manipulability ellipsoids. The 6-REXOS and a four-DoF exoskeleton robot are compared to verify the manipulation advantage due to the redundancy. The four-DoF exoskeleton robot is designed by excluding the two passive DoFs of the 6- REXOS. In addition, a kinematic model is proposed for the human lower arm to validate the performance of the 6- REXOS. Kinematic analysis and simulations are carried out to validate the 6-REXOS and human-lower-arm model.

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